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Red 33 (CI 17200). Mi Corazón Eau de Parfum. Alcohol Denat. Fragrance (Parfum).
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Cinnamyl acetate is an acetate ester, which is produced as a result of the formal condensation of cinnamyl alcohol with acetic acid. Its molecular formula is C 11 H 12 O 2 and is identified by various other names such as acetic acid cinnamyl ester, 1-acetoxy-3-phenyl-2-propene, etc. It is found in the essential oil of Cinnamon. About the Experts.
odor: sweet spicy cinnamyl mignonette hyacinth balsam. flavor: Spicy, cinnamon, balsamic, fruity, winey and honey-like with Functional use(s) - flavor and fragrance agents.
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2020-07-12 · Hello, I am working on a natural Amber, and I am desperately searching for cinnamyl alcohol and cinnamyl cinnamate in their natural isolate form. If you have any source I can buy from these compounds, this will be very helpful. cinnamic alcohol cinnamic aldehyde cinnamon bark oliffac 0912 cinnamyl acetate cis-3-hexenol (leaf alcohol) cis-3-hexenyl acetate (leaf acetate) cis-3-hexenyl benzoate cis-3-hexenyl salicylate (leaf salicylate) cis-6-nonenol cis-jasmone citral citral dimethyl acetal citralex gnr 0712 citralis pq citrolate citronellal citronellol 750 citronellol Appearance: Light Yellow Liquid Fragrance: Unique Scent Purity: 98%min Boiling Point: 219-220 Degree C Refractive Index (20 Degree C ): 1.604-1.608 Specific Gravity (20 Degree C ): 1.422-1.426 Packing: 200kg/plastic Drum Cinnamyl acetate is an acetate ester, which is produced as a result of the formal condensation of cinnamyl alcohol with acetic acid. Its molecular formula is C 11 H 12 O 2 and is identified by various other names such as acetic acid cinnamyl ester, 1-acetoxy-3-phenyl-2-propene, etc.
And as a major player in fragrances, our strong
Cinnamic alcohol is white crystalline solid when pure, or yellow oil when even slightly impure. It has the odour of hyacinth. Used in flavour, fragrances, and
It is a fragrant body, and may be used with good results in the pre- paration of hawthorn cinnamic alcohol, and phenyl propyl alcohol have been identified. AMYL CINNAMATE, 3487-99-8. ALPHA-AMYL CINNAMIC ALCOHOL, 101-85-9.
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Set includes Dish Soap, Liquid Hand Soap and Multi-Surface Everyday Cleaner. Garden-fresh Honeysuckle is a tempting sweet scent - a charming mix of flowers and fruits. Hazard Statement: May be harmful if swallowed. Causes serious eye irritation.
FL/FR, 3-, phenyl propyl alcohol. odor: sweet spicy cinnamyl mignonette hyacinth balsam. flavor: Spicy, cinnamon, balsamic, fruity, winey and honey-like with
Functional use(s) - flavor and fragrance agents. Evaluation 68 (FGE.68): Consideration of cinnamyl alcohol and related flavouring agents evaluated by JECFA
Category:flavor and fragrance agents Group Evaluation 68 (FGE.68): Consideration of cinnamyl alcohol and related flavouring agents evaluated by JECFA
Scientific Opinion on Flavouring Group Evaluation 68 (FGE.68): Consideration of cinnamyl alcohol and related flavouring agents evaluated by JECFA (55th
Functional use(s) - flavor and fragrance agents. Has an Recommendation for ( E)-cinnamyl acetate flavor usage levels up to: methyl cinnamyl alcohol. FR.
cinnamyl hexanoate cinnamyl caproate.
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Structure, properties, spectra, suppliers and links for: Cinnamyl alcohol, 104-54-1, 4407-36-7. We use synthetic cinnamyl alcohol to fragrance products with its green, spicy and floral scent. Functional use(s) - flavor and fragrance agents. Has a spicy type odor and an floral type flavor. FL/FR. alpha-.
ALPHA-AMYL CINNAMIC ALCOHOL, 101-85-9. ALPHA-AMYL CINNAMIC ALDEHYDE, 122-40-7. AMYL FORMATE, 638-49-3. Cinnamon leaf oil. Cinnamyl acetate. Cinnamyl alcohol. Cinnamyl cinnamate.
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About the Experts. Paula Begoun is the best-selling author of 20 books about skincare and makeup. She is known worldwide as The Cosmetics Cop and creator of Paula’s Choice Skincare. Cinnamyl acetate is an acetate ester, which is produced as a result of the formal condensation of cinnamyl alcohol with acetic acid. Its molecular formula is C 11 H 12 O 2 and is identified by various other names such as acetic acid cinnamyl ester, 1-acetoxy-3-phenyl-2-propene, etc.