| | | C<sub>9</sub>H<sub>8</sub>O | Cinnamal / (Cinnamic aldehyde) | | B-8,F-1,NA-6, NAE65-6, NAC80-6 | | | <img src="../IMAGES/pet.gif"/> | 3-Phenyl-2-propenal; Cinnamic aldehyde; 2-Propenal-3-phenyl; Cinnamal; Phenylacrolein; cassia aldehyde; 3-phenylpropenal; cinnamyl aldehyde; 3-phenylacrolein; benzylideneacetaldehyde; 3-phenyl-2-propenaldehyde; zimtaldehyde; 3-phenylacryaldehyde; Phenyl-2-propenal; Zimtaldehyde light; 3-Phenyl-2-propen-1-al. | Common ingredient in perfumes for household products like deodorizers, detergents, and soap. Flavor in toothpaste, sweets, ice cream, soft drinks, chewing gums, and cakes. Also present in balsam of Tolu and Peru, hyacinth plant, spices, cinnamon, Ceylon and cassia oil. Some Perfumery Uses : Canoe; Hyacinth; Bubblegum; Balsam; Cassia; Natural Occurrence : Cinnamon. Cross: cinnamic alcohol, cinnamon oil. May cause depigmentation. PA. ICU, NICU. | | | | <a href="PDF/P_InfoEn/C-014.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/C-014.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/C-014.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/C-014.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>9</sub>H<sub>10</sub>O | Cinnamyl alcohol / (Cinnamic alcohol) | | | | | <img src="../IMAGES/pet.gif"/> | Cinnamic Alcohol; 3-Phenyl-2-propen-1-ol; Styrone; gamma-Phenylallyl alcohol; Styrylcarbinol; Phenyl-2-propenol; Phenylallyl alcohol. | Component in perfumed cosmetic products and deodorants. Some Perfumery Uses : Cinnamon; Daffodil; Hyacinth; Jasmin. Natural Occurrence : Cinnamon. Cross: balsam Peru, propolis. May cause pigmentation of the face. | | | | <a href="PDF/P_InfoEn/C-013.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/C-013.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/C-013.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/C-013.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>14</sub>H<sub>18</sub>O | Amyl cinnamal / (Amylcinnamaldehyde) | | | | | <img src="../IMAGES/pet.gif"/> | Amylcinnamaldehyde, a-Amyl-cinnamaldehyde; a-Amylcinnamic aldehyde; Heptanal, 2-(phenylmethylene)-; 2-Benzylidene heptanal; 2-Pentyl-3-phenylpropenoic acid. | Raw material in the production of perfumes. Some Perfumery Uses : Tuberose; Peach; Cherry; Estee; Honeysuckle Chevrefeuille. Cross: amylcinnamic alcohol. | | | | <a href="PDF/P_InfoEn/A-014.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/A-014.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/A-014.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/A-014.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>10</sub>H<sub>12</sub>O<sub>2</sub> | | | B-2,DS-16,F-4, DMP-16,DMS-9 | | | <img src="../IMAGES/pet.gif"/> | 2-Methoxy-4-(2-propenyl)phenol; 1-Allyl-3-methoxy-4-hydroxybenzene; 2-Methoxy-4-allylphenol; 4-Allyl-2-methoxyphenol; 4-Allylguaiacol; Allylguaiacol; Caryophyllic acid; Eugenic acid; 4-allylcatechol-2-methyl ether; 4-allyl-1-hydroxy-2-methoxybenzene; 1-hydroxy-2-methoxy-4-prop-2-enylbenzene; 2-methoxy-4-prop-2-enylphenol; p-eugenol; 1,3,4-eugenol; 1-hydroxy-2-methoxy-4-allylbenzene; FA 100; fema no. 2467; 4-hydroxy-3-methoxyallylbenzene; 2-methoxy-1-hydroxy-4-allylbenzene; 1-allyl-4-hydroxy-3-methoxybenzene; 5-allylguaiacol; 1-hydroxy-4-allyl-2-methoxybenzene; 1-hydroxy-2-methoxy-4-propenylbenzene; 2-methoxy-4-(2-propen-1-yl)phenol; Allyl-2-methoxyphenol. | As fragrance in perfumery used as substitute for oil of cloves. Dental analgesic in impression materials and periodontal packings. In the production of vanillin. Insect attractant and component in inhalants and antiseptics. In the manufacture of flavorings. Some Perfumery Uses : Clove; Carnation; Cherry; Cinnamon; Spicy; Cross: balsam of Peru, isoeugenol, benzoin, propanidid. UCU. | | | | <a href="PDF/P_InfoEn/E-016.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/E-016.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/E-016.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/E-016.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>10</sub>H<sub>12</sub>O<sub>2</sub> | Isoeugenol (temporarily unavailable) | | | | | <img src="../IMAGES/pet.gif"/> | 2-Methoxy-4-(1-propenyl) phenol; 2-Methoxy-4-propenylphenol; 4-Hydroxy-3-methoxy-1-propenylbenzene; 4-Propenyl-2-methoxyphenol; 4-Propenylguaiacol; 1-hydroxy-2-methoxy-4-propenyl-(cis)benzene; 1-Hydroxy-2-methoxy-4-propen-1-yl benzene. | Manufacture of vanillin; perfumes; flavoring. Fragrance in perfumery, over-the-counter medicines, dental materials, foods. Some Perfumery Uses : Soap Gardenia; Coffee; Abronea; Tuberose; Jonquil. Natural Occurrence : Nutmeg Oil. Cross: eugenol | | | | <a href="PDF/P_InfoEn/I-002.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/I-002.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/I-002.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/I-002.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>10</sub>H<sub>18</sub>O | | | | | | <img src="../IMAGES/pet.gif"/> | (E)-3,7-Dimethyl-2,6-octadien-1-ol; 2-trans-3,7-dimethyl-2,6-octadiene-1-ol; trans-2,6-Dimethyl-2,6-octadien-8-ol; Lemonol; 2,6-dimethyl-trans-2,6-octadien-8-ol; 3,7-dimethyl-trans-2,6-octadien-1-ol; geranyl alcohol; guaniol; trans-3,7-Dimethyl-2,6-octadien-1-ol; trans-dimethyl-2,6-octadien-1-ol; Octadien-1-ol, 3,7-dimethyl-, (E)-; 2,6-Dimethyl-2,6-octadien-8-ol; Trans-3,7-dimethyl-2,7-octadien-1-ol. | In perfumery; a synthetic flavoring substance and adjuvant. As insect attractant. Some Perfumery Uses: Peony; Rose Centifolia; Magnolia; Orange Juice; Petitgrain Lemon Petitgrain; Natural Occurrence: Rose. | | | | <a href="PDF/P_InfoEn/G-001.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/G-001.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/G-001.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/G-001.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | | | | | | | <img src="../IMAGES/pet.gif"/> | | | | | | <a href="PDF/P_InfoEn/O-001.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/O-001.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/O-001.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/O-001.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>10</sub>H<sub>18</sub>O<sub>2</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | 7-Hydroxydihydrocitronellal; 3,7-Dimethyl-7-hydroxyoctan-1-al; Hydroxycitronellal dimethylacetal; 3,7-dimethyl-7-hydroxyoctanal; 7-hydroxy-3,7-dimethyloctanal; Cyclalia; Cyclosia; Laurine; Phixia. | Fragrance for use in various perfumes, antiseptics, insecticides and household products. Some Perfumery Uses : Sweet Pea Pois De Senteur; Gardenia; Cherry; Melon; Mint; Cross: citronellal, geranial, methoxycitronellal. May produce hyperpigmentation. | | | | <a href="PDF/P_InfoEn/H-008.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/H-008.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/H-008.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/H-008.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | | Narcissus Poeticus / (Narcissus absolute) | | | | | <img src="../IMAGES/pet.gif"/> | Narcissus jonquilla l. absolute; Narcissus absolute; Narcissus spp. Absolute. | A very scarce and, partly for that reason, very rarely used perfume material is the flower absolute from the Narcissus Jonquilla. This very fragrant narcissus species probably originated in Asia Minor and it is cultivated in the Grasse region of southern France and in Morocco for the purpose of extracting perfume oil. The flowers are extracted with petroleum ether to yield a concrete which in turn is processed to an absolute. Jonquil Absolute from Concrete is a viscous, dark brown or dark orange to olive brown liquid of heavy, honey like, deep sweet floral odor with a strong green backnote and a somewhat bitter, very tenacious dryout note. The odor bears great similarity to the fragrance of longoza and tuberose and a resemblance to hyacinth. Dark brown viscous oil extract from the flowers of Narcissus. Some Perfumery Uses: Joy; Hyacinth; Jonquil; Tuberose. | | | | <a href="PDF/P_InfoEn/N-006.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/N-006.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/N-006.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/N-006.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>12</sub>H<sub>15</sub>N<sub>3</sub>O<sub>6</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | Musk xylol; Benzene, 1-(1,1-dimethylethyl)-3,5-dimethyl-2,4,6-trinitro-; 5-tert-butyl-2,4,6-trinitro-m-xylene; 2,4,6-Trinitro-1,3-dimethyl-5-tert-butylbenzene. | Synthetic nitro musk compound for use as fragrance and fixative in after shave lotions, perfumes etc. The musk compound of choice for soap and detergent fragrances. Some Perfumery Uses: Soap; Norell; Oriental; Chypre; Herbal; Cross (photo): musk ambrette. PA. | | | | <a href="PDF/P_InfoEn/M-021.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/M-021.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/M-021.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/M-021.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | | | | | | | <img src="../IMAGES/pet.gif"/> | Used in a wide variety of fragrances and flavors. Perfume for ointments and in the manufacture of synthetic perfumes; flavorings. Odor descriptions: orange-flower, fruity, grape-like odor. Some perfumery | cherry, banana, strawberry, blueberry, grape. Natural occurence: grape, concord. | | | | <a href="PDF/P_InfoEn/M-028.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/M-028.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/M-028.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/M-028.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>14</sub>H<sub>18</sub>N<sub>2</sub>O<sub>4</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | | Synthetic nitro musk compound for use as fragrance and fixative in after-shave lotions, perfumes, etc. | | | | <a href="PDF/P_InfoEn/M-019.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/M-019.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/M-019.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/M-019.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | | | | | | | <img src="../IMAGES/pet.gif"/> | Arlacel 83; Sorbitan, (Z)-9-octadecenoate (2:3). Mixed ester of oleic acid and hexitol anhydrides derived from sorbitol. | Emulsifier in cosmetic and pharmaceutical ointments and creams. | | | | <a href="PDF/P_InfoEn/S-005.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/S-005.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/S-005.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/S-005.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | | | | | | | <img src="../IMAGES/pet.gif"/> | | Synthetic jasmine for use as fragrance in perfumery. Cross: benzylsalicylate. | | | | <a href="PDF/P_InfoEn/J-001.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/J-001.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/J-001.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/J-001.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>14</sub>H<sub>12</sub>O<sub>3</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | 2-Hydroxybenzoic acid phenylmethyl ester; Salicylic acid benzyl ester; benzyl o-hydroxybenzoate; Benzoic acid, 2-hydroxy, phenyl methyl ester. | Organic solvent for perfumes (some Perfumery Uses : Chloe; Anais Anais; Estee; Plum; Lily); organic synthesis; pharmaceuticals; tanning creams and lotions. Natural Occurrence : Dianthus Caryophyllus L. May cause pigmentation of the face. | | | | <a href="PDF/P_InfoEn/B-010B.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/B-010B.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/B-010B.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/B-010B.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>7</sub>H<sub>8</sub>O | | | P-12,C-34,F-16, NAE65-59, NAC80-58 | | | <img src="../IMAGES/aq.gif"/> | Benzenemethanol; Phenylcarbinol; Phenylmethyl alcohol; Phenylmethanol; alpha-Hydroxytoluene; Benzoyl alcohol; Hydroxytoluene; Benzenecarbinol; alpha-toluenol; (hydroxymethyl)benzene. | This compound is used as a photographic developer for color movie film and in perfumes, flavor industries, pharmaceuticals as a bacteriostatic, cosmetics, ointments, emulsions, textiles, sheet plastics and inks. It is a solvent for dyestuffs, cellulose esters, cellulose acetate, casein, gelatin, waxes and shellac. It is used as an intermediate for benzyl esters and ethers, as a surfactant, an insect repellent, local anesthetic, preservative in radio- pharmaceuticals and preservative in sterile solutions for intramuscular or intravenous use. It is used in heat-sealing polyethylene films, dyeing nylon filament and in microscopy as an embedding material. In veterinary medicine, it has been used for relief from pruritus. It once was used as an antiseptic. Some Perfumery Uses : Enhancer; Cacao; White Rose; Fixer; Hyacinth Jacinthe; Natural Occurrence : Tea. Cross: balsam Peru, benzoin tincture. May cause pigmentation of the face. ICU | | | | <a href="PDF/P_InfoEn/B-008B.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/B-008B.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/B-008B.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/B-008B.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>8</sub>H<sub>8</sub>O<sub>3</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | 4-Hydroxy-3-methoxybenzaldehyde; 3-Methoxy-4-hydroxybenzaldehyde; Methylprotocatechuic aldehyde; Vanillic aldehyde; Vanillaldehyde; Hydroxy-3-methoxybenzaldehyde; Lure-n-kill fly tape; Methoxy-4-hydroxybenzaldehyde. | Flavoring agent in beverages, confectionery, foods, galenicals. In perfumery and pharmaceuticals. As chemical reagent. Some Perfumery Uses: Passion Fruit; Almond; Pear; Confectionary Flavors; Melon; Natural Occurrence: Clove Bud Oil.
Cross: Coumarin, propolis. NICU | | | | <a href="PDF/P_InfoEn/V-001.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/V-001.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/V-001.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/V-001.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | | Lavender absolute/(Lavandula) | | | | | <img src="../IMAGES/pet.gif"/> | Garden lavender; True Lavender; Oils, lavender; Lavender; Lavender oil; Lavandula angustifolia absolute; Lavender absolute; Lavandula angustifolia oil; Lavandula angustifolia oil bulgarian; Lavandula angustifolia concrete; Lavender concrete; Lavandula officinalis oil french; Oil of Lavender. | Lavender Oil is steam distilled from the freshly cut flowering tops and stalks of Lavandula Officinalis, a wild growing or cultivated plant, native to the Mediterranean countries. Distillation takes place mainly in the south of France where the plants grow at medium altitudes of this mountainous region. Lavender Oil is a colorless or pale yellow liquid of sweet, floral herbaceous refreshing odor with a pleasant, balsamic woody backnote. Fragrance for use in various perfumes. Flavor and carminative. Some Perfumery Uses : Hay New Mown Hay; Herbal; Tabac; Amber; Fern;
Cross: GeraniaL. | | | | <a href="PDF/P_InfoEn/L-001.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/L-001.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/L-001.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/L-001.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | | | | | | | <img src="../IMAGES/pet.gif"/> | cananga odorata hook f. and thomas; oil java | Fragrance for use in various perfumes. Examples of usage: Lily; Carnation Dianthus Oeillet; Hyacinth Jacinthe; Narcissus Narcisse Cross: benzyl salicylate. May cause pigmentation of the face. Botanical origin Cananga odorata. It is the total amount of oil by steam distillation.
The CAS number is 68606-83-7
The colour is yellow. The oil used by Chemotechnique is harvested on Java. Other places for Producing Cananga oil are Madagaskar, Reunion, Mauritius and Comoro.
Contains among other substances Benzoic acid, beta-Caryophyllene, alpha-Humulene, (E,E)-Farnasene, gamma-Cadinene, delta-Cadinene, Benzyl benzoate, Linalool and Geranyl acetate. | | | | <a href="PDF/P_InfoEn/C-002.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/C-002.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/C-002.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/C-002.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | | | | | | | <img src="../IMAGES/pet.gif"/> | Rose Oil; Rose oil, Bulgarian; Otto of rose; essence of Rose; Attar of Rose; Oils, rose; Concrete rose Bulgarian; Concrete rose morocco; Concrete rose Turkish; Integral rose; Rose blossom oil; Rose centifolia oil; Rose concrete; Rose Damascena oil; Rose De Mai oil; Rose leaf oil; Rose oil, Damascena; Rose Otto Turkish Extra; Rosewood oil; Stearoptenes, rose; Turkish rose otto; Rosa damascena mill. absolute bulgarian; Rose absolute bulgarian; Attar of roses; Rose oil otto; Rose oil egyptian; Rose oil moroccan; Rose absolute. | Fragrance for use in various perfumes. For flavoring lozenges, ointments, toilet preparations etc. Forms an important part of the conventional rose jasmin complex which is found in countless fashion perfumes. It is used in cassie modifications, carnation bases and fantasy bouquets. Examples of usage: Carnation Dianthus Oeillet; Violet; Nahema 4.5% of the oil; Orangeflower Fleur D’oranger. | | | | <a href="PDF/P_InfoEn/R-003.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/R-003.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/R-003.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/R-003.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | | Cananga odorata oil / (Ylang-Ylang oil) | | F-21,NA-16,NAE65-65, NAC80-57 | | | <img src="../IMAGES/pet.gif"/> | Ylang-Ylang oil; Anona oil; Cananga odorata hook absolute; Ylang ylang absolute; Cananga odorata hook. f. and thomas. Oil. | Fragrance for use in various perfumed products. The oil is useful in soap perfumes and in general perfumery as a floral additive of extremely versatile application. It blends with almost any other floral natural or synthetic material and gives good effects in a concentration of 0.5% up to about 5% of the perfume base. Main aromatic component is methyl anthranilate. Some Perfumery Uses: Candy; Modifier And Fixer In Floral; Ylang; Hyacinth Jacinthe; Muguet Lily Of The Valley; Lily; Carnation Dianthus Oeillet; Hyacinth Jacinthe; Narcissus Narcisse. Extracted by steam distillation from flowers of the tree Cananga Odorata (botanical name).
The total amount of oil is traded as Cananga oil but Ylang Ylang is fractioned into about 4 different grades. The first fraction is Ylang Ylang Extra and this one is used by Chemotechnique and the perfume industry. It is the finest part and contains 20-40% of the whole distillate. The CAS number for this is 8006-81-3. The following fractions are used in soap, cosmetics etc. It contains among other substances Methyl anthranilate, (E,E)-Farnesene, delta-Cadinene, p-Methyl anisole, Linalool, Geranyl acetate, beta-Caryophyllene, p-Cresylmethyl ether, Methyl benzoate, Benzyl acetate and Benzyl benzoate.
Mostly contributing to its odor are p-cresol, eugenol and isoeugenol.
Cross: Benzyl salicylate, geranial. May cause pigmentationof the face. | | | | <a href="PDF/P_InfoEn/Y-001.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/Y-001.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/Y-001.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/Y-001.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | | | | | | | <img src="../IMAGES/pet.gif"/> | | | | | | <a href="PDF/P_InfoEn/G-002.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/G-002.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/G-002.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/G-002.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | | | | | | | <img src="../IMAGES/pet.gif"/> | Jasmine absolute, Egyptian. | Natural jasmine for use as fragrance in perfumery. Used extensively in in grand perfumes as well as ordinary perfumes and bases. Examples of usage: Lily; Lilac Lilas; Honeysuckle Chevrefeuille; Muguet Lily of the Valley. Cross: benzylsalicylate.
May produce hyperpigmentation. | | | | <a href="PDF/P_InfoEn/J-002.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/J-002.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/J-002.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/J-002.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | | Santalum album oil / (Sandalwood oil (Indian) | | | | | <img src="../IMAGES/pet.gif"/> | Arheol; East Indian sandalwood oil; Oil of Santal; Oils, sandalwood; Sandlewood oil. | Fragrance for use in various perfumed products like soap, after-shave lotions, colognes and cosmetics. Examples of usage: Mimusops; Cedarwood; Clary Sage; Casteoreum. PA. PT. PL. | | | | <a href="PDF/P_InfoEn/S-009.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/S-009.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/S-009.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/S-009.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>13</sub>H<sub>22</sub>O<sub>2</sub> | Hydroxyisohexyl 3-Cyclohexene Carboxaldehyde (Lyral) (Temporarily unavailable) | | F-25,S-28, IS-27,NAE65-58, NAC80-72, | | | <img src="../IMAGES/pet.gif"/> | 3-cyclohexene-1-carboxaldehyde, 4-(4-hydroxy-4-methyl pentyl) | Fragrance known for it´s soft delicate floral, lily, cyclamen note reminiscent of hydroxycitronellal. Used in producs such as Alcoholic Lotion, Anti Perspirant, Deo Stick, Detergent Perborate, Detergent TAED, Fabric Softener, Hard Surface Cleaner, Shampoo and soap. Stabilized with 0.1% BHT | | | | <a href="PDF/P_InfoEn/L-003.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/L-003.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/L-003.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/L-003.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>10</sub>H<sub>16</sub>O | | | | | | <img src="../IMAGES/pet.gif"/> | Geranial; Geranialdehyde;
3,7-Dimethyl-2,6-octadienal; cis-3,7-Dimethyl-2,6-octadienal; cis-Citral; cis/trans-3,7-Dimethyl-2,6-octadienal; Citral A; citral-b; mixture of cis and trans Citral ; Lemarome n; Neral; Mixture of (E)-3,7-Dimethyl-2,6-octadienal and (Z)-3,7-Dimethyl-2,6-octadienal | Fragrance for use in various perfumes. Examples of usage: in citrus notes and floral fragrance blends and as an intermediate to form other compounds. | | | | <a href="PDF/P_InfoEn/C-036.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/C-036.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/C-036.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/C-036.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>15</sub>H<sub>26</sub>O | Farnesol/(2,6,10-Dodecatrien-1-ol,3,7,11 trimethyl) | | | | | <img src="../IMAGES/pet.gif"/> | 3,7,11-trimethyl-2,6,10-dodecatrien-1-ol | Farnesol is a natural organic compound which is a sesquiterpene alcohol found as a colorless liquid. It is insoluble in water, but miscible with oils.
It is present in many essential oils such as citronella, neroli, cyclamen, lemon grass, tuberose, rose, musk, balsam and tolu. It is used in perfumery to emphasize the odors of sweet floral perfumes.
Farnesol is also a natural pesticide for mites and is a pheromone for several other insects.
In a 1994 report released by five top cigarette companies, farnesol was listed as one of 599 additives to cigarettes. It is a flavoring ingredient. | | | | <a href="PDF/P_InfoEn/F-004.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/F-004.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/F-004.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/F-004.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>10</sub>H<sub>20</sub>O | | | | | | <img src="../IMAGES/pet.gif"/> | 3,7-dimethyl-6-Octen-1-ol; dL-Citronellol;
Cephrol; Rhodinol; Levo-citronellol; Cephrol; Beta-citronellol; 2,6-Dimethyl-2-octen-8-ol; Rodinol; | Citronella is the common name for a grassa,Cymbopogon nardus, which is native to India and southeast Asia. Citronella oil is a yellowish essential oil distilled from the leaves of either of two grasses, Cymbopogon nardus or C. winterianus. This aromatic oil is inexpensive, and widely used in cheap perfumes and as a fragrance in soaps. It is also best known as an insect repellent. Citronellol, derived form citronella oil, is a chief constituent of geranium oil, another is geraniol. Both are used in the production of perfumes. (sweet, rose, lilac, geranium ) . | | | | <a href="PDF/P_InfoEn/C-037.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/C-037.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/C-037.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/C-037.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>15</sub>H<sub>200</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | 3,7-dimethyl-6-Octen-1-ol; dL-Citronellol;
Cephrol; Rhodinol; Levo-citronellol; Cephrol; Beta-citronellol; 2,6-Dimethyl-2-octen-8-ol; Rodinol; | Fragrance for use in various perfumed products. Odor Profile Floral, Jasmin, Waxy. Olfactory Description: Similar to alpha amyl cinnamic aldehyde but with a finer, more floral and delicate character. Found in Acid Cleaner Liquid, Detergent TAED, Alcoholic Lotion, Fabric Softener, Anti Perspirant, Foam Bath, Bleach, Hard Surface Cleaner, Deo Stick Shampoo, Detergent Perborate. Soap. | | | | <a href="PDF/P_InfoEn/H-025.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/H-025.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/H-025.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/H-025.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>9</sub>H<sub>6</sub>O<sub>2</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | ,2-Benzopyrone; 2-Oxo-1,2-benzopyran;
3-(2-hydroxyphenyl)-delta-lactone-2-Propenoic acid; Tonka bean camphor; Coumaric Acid; cis-o-Coumaric acid lactone; 2H-1-Benzopyran-2-one; 2-Oxo-2H-1-benzopyran; cis-O-coumarinic acid lactone; benzo-alpha-pyrone; o-hydroxycinnamic acid deltalactone; coumarinic anhydride; o-hydroxycinnamic acid lactone; o-hydroxycinnamic lactone; coumarinac lactone; 2H-benzopyran-2-one; Benzo-2-pyrone; Benzopyran-2-one; 3-(2-hydroxyphenyl)-Propenoic acid, delta-lactone; Cumarin (German); Cumarina (Spanish); Coumarine (French); | Coumarin (anhydride of o-coumaric acid) is white, crystalline lactone, obtainable naturally from several plants, such as tonka bean, lavender, sweet clover grass, strawberries, and cinnamon, or produced synthetically from an amino acid, phenylalanine. It is the principle of dicumarol which inhibits the hepatic synthesis of the vitamin K–dependent coagulation factors. Coumarin derivatives are used widely as anticoagulants (such as warfarin, -OH group is attached at 4 position) for the treatment of disorders in which there is excessive or undesirable clotting, such as thrombophlebitis, pulmonary embolism, and certain cardiac conditions. Coumarin derivatives are also used as rodenticides due to the property of causing fatal hemorrhaging. Coumarin has the characteristic odour like that of vanilla beans. It is used for the preparation of perfumes, soaps, flavourings. The coumarin nucleus (benzo-2-pyrone) is derived cinnamic acid (phenylacrylic skeleton) in the biosynthesis. Accordingly, the hydroxy group attached to coumarin structure at 7 position is important in biosynthesis pathway. Umbelliferone (7-hydroxy coumarin), esculetin (6,7-Dihydroxycoumarin), scopoletin (7-hydroxy-6-methoxycoumarin) are the widespread coumarins in nature. Synthetic 7-hydroxy coumarins are used to absorb ultraviolet rays in sunscreen cosmetics and used in the synthesis of drugs especially anticancer. | | | | <a href="PDF/P_InfoEn/C-038.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/C-038.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/C-038.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/C-038.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | | | | F-31, NA-32,S-27, NAE65-32, NAC80-50, IS-25 | | | <img src="../IMAGES/pet.gif"/> | Mix of 6 fragrance ingredients commonly causing dermatitis from use of perfumed products. For information, see individual allergens. | | | | | <a href="PDF/P_InfoEn/MX-25.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/MX-25.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/MX-25.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/MX-25.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>14</sub>H<sub>20</sub>O | | | | | | <img src="../IMAGES/pet.gif"/> | | | | | | <a href="PDF/P_InfoEn/A-036.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/A-036.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/A-036.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/A-036.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>8</sub>H<sub>10</sub>O<sub>2</sub> | | | | | | <img src="../IMAGES/aq.gif"/> | | | | | | <a href="PDF/P_InfoEn/A-037.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/A-037.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/A-037.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/A-037.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>20</sub>H<sub>30</sub>O<sub>2</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | 1/C14H12O2/c15-14(13-9-5-2-6-10-13)16-11-12-7-3-1-4-8-12/h1-10H,11H, 120-51-4, 4-09-00-00307 (Beilstein Handbook Reference), AI3-00523, AIDS-018031, AIDS018031, Antiscabiosum, Ascabin, Ascabiol, Benylate, Benylate (TN), Benzoesaeurebenzylester, BENZOIC ACID PHENYLMETHYLESTER, Benzoic acid, benzyl ester, Benzoic acid, phenylmethyl ester, BENZOIC ACID,BENZYL ESTER, Benzyl alcohol benzoic ester, Benzyl benzenecarboxylate, Benzyl Benzoate, Benzyl benzoate (JP14/USP), Benzyl benzoate (natural), Benzyl benzoate [USAN:JAN], Benzyl phenylformate, Benzylbenzenecarboxylate, Benzylester kyseliny benzoove [Czech], Benzylets, Benzylis benzoas, Benzylum benzoicum, BRN 2049280, BZM, C12537, Caswell No. 082, Colebenz, D01138, DivK1c_000204, EINECS 204-402-9, EPA Pesticide Chemical Code 009501, FEMA No. 2138, FEMA Number 2138, HSDB 208, KBio1_000204, KBio2_001720, KBio2_004288, KBio2_006856, KBio3_002714, KBioGR_001186, KBioSS_001720, NINDS_000204, Novoscabin, NSC 8081, NSC8081, Peruscabin, Peruscabina, Phenylmethyl benzoate, Scabagen, Scabanca, Scabide, Scabiozon, Scabitox, Scobenol, Spasmodin, SPBio_000543, Spectrum2_000532, Spectrum3_001757, Spectrum4_000773, Spectrum_001240, Vanzoate, Venzonate, ZINC00001021 | Benzyl benzoate is the ester of benzyl alcohol and benzoic acid. This easily prepared compound has a variety of uses. Benzyl benzoate, as a topical solution, may be used as an antiparasitic insecticide to kill lice and the mites responsible for the skin condition scabies. It has other uses such as a fixative in fragrances to improve the stability and other characteristics of the main ingredients; a food additive in artificial flavors; a plasticizer in cellulose and other polymers; a solvent for various chemical reactions; a treatment for sweet itch in horses. | | | | <a href="PDF/P_InfoEn/B-038.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/B-038.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/B-038.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/B-038.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>16</sub>H<sub>14</sub>O<sub>2</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | 103-41-3, 2-Propenoic acid, 3-phenyl-, phenylmethyl ester, 2-Propenoic acid, 3-phenyl-, phenylmethyl ester, (E)-, 3-Phenyl-2-propenoic acid phenylmethyl ester, 3-Phenyl-acrylic acid, benzyl ester, 8014-16-2, AI3-01268, AIDS-224206, AIDS224206, Benzyl (2E)-3-phenyl-2-propenoate, Benzyl 3-phenylpropenoate, Benzyl alcohol, cinnamate, Benzyl alcohol, cinnamic ester, BENZYL CINNAMATE, Benzyl gamma-phenylacrylate, Benzyl-3-phenylpropenoate, Benzylcinnamate, Benzylcinnamoate, Benzylester kyseliny skoricove [Czech], Cinnamein, Cinnamic acid, benzyl ester, EINECS 203-109-3, FEMA No. 2142, HSDB 359, NSC 11780, Phenylmethyl 3-phenyl-2-propenoate, trans-Cinnamic acid benzyl ester | Benzyl Cinnamate is a common used flavoring agent (sweet, floral, fruity) and used as a perfumery fixer. | | | | <a href="PDF/P_InfoEn/B-039.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/B-039.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/B-039.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/B-039.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>14</sub>H<sub>20</sub>O | Butylphenyl methylpropional (Lilial) | | | | | <img src="../IMAGES/pet.gif"/> | | | | | | <a href="PDF/P_InfoEn/B-040.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/B-040.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/B-040.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/B-040.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | | | | | | | <img src="../IMAGES/pet.gif"/> | Evernia furfuracea, ext; Tre moss. | (Psued) Evernia furfuracea (tree moss) is a lichen that grows on the bark of firs and pines. The lichen is rather sensitive to air pollution, its presence usually indicating the good air conditions in the growing place. In ancient Egypt it was also found packed into mummies. | | | | <a href="PDF/P_InfoEn/E-026.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/E-026.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/E-026.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/E-026.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>14</sub>H<sub>22</sub>O | | | | | | <img src="../IMAGES/pet.gif"/> | .alpha.-Cetone, .alpha.-Ionone, isomethyl-, .alpha.-Isomethylionone, 127-51-5, 3-Buten-2-one, 3-methyl-4- (2,6,6-trimethyl-2-cyclohexen-1-yl)-, 3-Buten-2-one, 3-methyl-4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-, 4-(2,6, 6-Trimethyl-2-cyclohexen-1-yl)-3-methyl-3-buten-2-one, 4-(2,6,6-Trimethyl-2-cyclohexen-1-yl)-3-methyl-3-buten-2-one, Cetone alpha, Iso-.alpha.-methyl ionone, Isomethyl-.alpha.-ionone, Methyl-.alpha.-isoionone, NSC66432 | alfa-Isomethyl ionone is used in many floral fragrances, particularly violet. Blends with and supports woody, leathery, and oriental accords. | | | | <a href="PDF/P_InfoEn/I-017.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/I-017.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/I-017.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/I-017.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>10</sub>H<sub>16</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | (+)-4-Isopropenyl-1-Methylcyclohexene; (+)-R-Limonene; Citrene; D-(+)-Limonene (+)-p-menth-1,8-diene; Carvene; Optical Isomer of Dipentene; (R)-1-Methyl-4-(1-Methylethyenyl); Cyclohexene. | Limonene is a hydrocarbon, classified as a cyclic terpene. It is a colourless liquid at room temperatures with an extremely strong smell of oranges. It takes its name from the lemon, as the rind of the lemon, like other citrus fruits, contains considerable amounts of this chemical compound, which is responsible for much of their smell. Limonene is a chiral molecule, and as is common with such forms, biological sources produce one enantiomer: the principal industrial source, citrus fruit, contains D-limonene ((+)-limonene), which is the (R)-enantiomer (CAS number 5989-27-5, EINECS number 227-813-5). Racemic limonene is known as dipentene. | | | | <a href="PDF/P_InfoEn/L-006C.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/L-006C.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/L-006C.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/L-006C.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>10</sub>H<sub>18</sub>O | | | | | | <img src="../IMAGES/pet.gif"/> | Linalool, synthetic, ( )-linalool, (+-)-Linalool, (1)-3,7-Dimethyl-1,6-octadien-3-ol, (R)-3,7-Dimethyl-1,6-octadien-3-ol, (S)-Linalol, .beta.-Linalool, 0-01-00-00462 (Beilstein Handbook Reference), 1, 6-Octadien-3-ol, 3,7-dimethyl-, (-)-, 1,6-Octadien-3-ol, 3,7-dimethyl-, 1,6-OCTADIEN-3-OL, 3,7-DIMETHYL-, (-)-, 1,6-Octadien-3-ol, 3,7-dimethyl-, (3R)-, 11024-20-7, 126-91-0, 2,6-Dimethyl-2, 7-octadiene-6-ol, 2,6-Dimethyl-2,7-octadien-6-ol, 2,6-Dimethyl-2,7-octadiene-6-ol, 2,6-Dimethylocta-2,7-dien-6-ol, 2,7-Octadien-6-ol, 2,6-dimethyl-, 22564-99-4, 3,7-Dimethyl-1, 6-octadien-3-ol, 3,7-Dimethyl-1,6-octadien-3-ol, 3,7-Dimethylocta-1,6-dien-3-ol, 78-70-6, AI3-00942, AIDS-032328, AIDS032328, allo-Ocimenol, beta-Linalool, BRN 1721488, C03985, Caswell No. 526A, CCRIS 3726, CCRIS 6557, CHEBI:17580, EINECS 201-134-4, EINECS 204-811-2, EINECS 245-083-6, EPA Pesticide Chemical Code 128838, FEMA No. 2635, FEMA Number 2635, HSDB 645, L-Linalool, Linalol, Linalool, Linalool (natural), Linalyl alcohol, LINOLOOL (D), LS-1752, NSC 3789, NSC3789, p-Linalool | Linalool is a naturally-occurring terpene alcohol chemical found in many flowers and spice plants with many commercial applications, the majority of which are based on its pleasant scent (floral, with a touch of spiciness). Is a main constituent of oils of rosewood, Ho, lavender, lavandin, clary sage, bergamot, petitgrain; minor of neroli, tangerine, and jasmine.
It has other names such as â-linalool, linalyl alcohol, linaloyl oxide, p-linalool, allo-ocimenol and 2,6-dimethyl-2,7-octadien-6-ol. | | | | <a href="PDF/P_InfoEn/L-005B.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/L-005B.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/L-005B.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/L-005B.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>9</sub>H<sub>14</sub>O<sub>2</sub> | | | | | | <img src="../IMAGES/pet.gif"/> | | | | | | <a href="PDF/P_InfoEn/M-034.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/M-034.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/M-034.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/M-034.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | C<sub>12</sub>H<sub>18</sub> O | Majanthole/ (2,2-dimethyl-3-(3-pethylphenyl)propan1-ol) | | | | | <img src="../IMAGES/pet.gif"/> | 2,2-dimethyl-3-(3-pethylphenyl)propan-1-ol. | Majanthole has a fresh and intensely floral note. The recommended use level of this colorless liquid-to-crystalline product is 5–20%. This ingredient can be used in lily of valley and fruity floral fragrances for detergent powder, fabric softener and soap applications. | | | | <a href="PDF/P_InfoEn/M-033.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/M-033.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/M-033.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/M-033.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | | Hydroperoxides of Linalool | | F-43,NA-40,NAE65-40,NAC80-74 | | | <img src="../IMAGES/pet.gif"/> | | Linalool is found in fine fragrances, cosmetics, and hygiene products as well as in household and industrial products. Linalool is among the most commonly found fragrance ingredients in consumer products presently available. Linalool is a naturally occurring terpene, present in large amounts in various plants, for example in lavender, rosewood, bergamot and jasmine. Linalool autoxidize on air exposure at room temperature forming hydroperoxides. Compared to pure unoxidized linalool the hydroperoxides of oxidized linalool have shown to be far more allergenic. NOTE: The preparation contains oxidized linalool. The concentration of the active haptens in the preparation is measured from the added amount of the hydroperoxides of linalool. | | | | <a href="PDF/P_InfoEn/H-031A.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/H-031A.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/H-031A.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/H-031A.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | | Hydroperoxides of Limonene | | F-44,O-27,B-15,NA-36,NAE65-36,NAC80-60 | | | <img src="../IMAGES/pet.gif"/> | Limonene is found in cosmetics, fine fragrances and hygiene products as
well as in household and industrial products. Limonene is one of the most commonly found fragrance ingredients in consumer products presently available. Limonene is a naturally occurring terpene, present in large amounts in various citrus fruits. Limonene autoxidize on air exposure at room temperature
forming hydroperoxides. Compared to pure unoxidized limonene the
hydroperoxides of oxidized limonene have shown to be far more allergenic. NOTE: The preparation contains 3% oxidized limonene. The concentration of the active haptens in the preparation is measured from the added amount of the hydroperoxides of d-limonene. | | | | | <a href="PDF/P_InfoEn/H-032A.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/H-032A.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/H-032A.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/H-032A.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | | | | S-19,NA-28,IS-12, NAE65-28, NAC80-28 | | | <img src="../IMAGES/pet.gif"/> | <p>Mix of various fragrance ingredients commonly causing dermatitis from perfumed products. Contains 5% Sorbitan sesquioleate as emulsifier.</p> | | | | | <a href="PDF/P_InfoEn/MX-07.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/MX-07.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/MX-07.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/MX-07.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | | Hydroperoxides of Linalool | | | | | <img src="../IMAGES/pet.gif"/> | | Linalool is found in fine fragrances, cosmetics, and hygiene products as well as in household and industrial products. Linalool is among the most commonly found fragrance ingredients in consumer products presently available. Linalool is a naturally occurring terpene, present in large amounts in various plants, for example in lavender, rosewood, bergamot and jasmine. Linalool autoxidize on air exposure at room temperature forming hydroperoxides. Compared to pure unoxidized linalool the hydroperoxides of oxidized linalool have shown to be far more allergenic. NOTE: The preparation contains oxidized linalool. The concentration of the active haptens in the preparation is measured from the added amount of the hydroperoxides of linalool. | | | | <a href="PDF/P_InfoEn/H-031B.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/H-031B.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/H-031B.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/H-031B.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |
| | | | Hydroperoxides of Limonene | | | | | <img src="../IMAGES/pet.gif"/> | Carvene, (+)-4-Isopropenyl-1-Methylcyclohexene, Optical Isomer of Dipentene, (+)-R-Limonene, (R)-1-Methyl-4-(1-Methylethyenyl) Cyclohexene, D-(+)-Limonene | Limonene is found in cosmetics, fine fragrances and hygiene products as well as in household and industrial products. Limonene is one of the most commonly found fragrance ingredients in consumer products presently available. Limonene is a naturally occurring terpene, present in large amounts in various citrus fruits. Limonene autoxidize on air exposure at room temperature forming hydroperoxides. Compared to pure unoxidized limonene the hydroperoxides of oxidized limonene have shown to be far more allergenic. NOTE: The preparation contains 3% oxidized limonene. The concentration of the active haptens in the preparation is measured from the added amount of the hydroperoxides of d-limonene. | | | | <a href="PDF/P_InfoEn/H-032B.pdf" Target="_blank">English</a> | <a href="PDF/P_InfoFr/H-032B.pdf" Target="_blank">French</a> | <a href="PDF/P_InfoSp/H-032B.pdf" Target="_blank">Spanish</a> | <a href="PDF/MSDS/H-032B.pdf" Target="_blank">SDS</a> | <a href="PDF/TestFrm/F-1000.pdf" Target="_blank">English</a> | <a href="PDF/TestFrm/Prev/F-1000.pdf" Target="_blank">Previous Year</a> | |