10402-47-8 Usage
Description
Geranyl valerate is a colorless liquid with a fruity pineapple aroma, which is characterized by its medium strength odor and floral type. It is commonly found in various plant sources such as geranium leaf oil, geranium oil, geranium petiole oil, geranium stem oil, and sassafras leaves.
Uses
Used in Flavor Industry:
Geranyl valerate is used as a flavoring agent for its fruity pineapple aroma, adding a pleasant and distinct taste to various food and beverage products.
Used in Fragrance Industry:
Geranyl valerate is used as a fragrance ingredient for its medium strength, floral odor. It is widely utilized in the creation of perfumes, colognes, and other scented products to provide a fresh and appealing scent.
Used in Aromatherapy:
Due to its fruity and floral aroma, geranyl valerate is used in aromatherapy as a natural essential oil to promote relaxation, reduce stress, and create a soothing atmosphere.
Used in Cosmetics and Personal Care Products:
Geranyl valerate is used as a key ingredient in cosmetics and personal care products, such as lotions, creams, and shampoos, for its pleasant scent and potential benefits to the overall sensory experience of the products.
Check Digit Verification of cas no
The CAS Registry Mumber 10402-47-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,0 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10402-47:
(7*1)+(6*0)+(5*4)+(4*0)+(3*2)+(2*4)+(1*7)=48
48 % 10 = 8
So 10402-47-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H26O2/c1-5-6-10-15(16)17-12-11-14(4)9-7-8-13(2)3/h8,11H,5-7,9-10,12H2,1-4H3/b14-11+
10402-47-8Relevant articles and documents
Efficient O-Acylation of Alcohols and Phenol Using Cp2TiCl as a Reaction Promoter
Durán-Pe?a, María Jesús,Botubol-Ares, José Manuel,Hanson, James R.,Hernández-Galán, Rosario,Collado, Isidro G.
supporting information, p. 3584 - 3591 (2016/07/28)
A method has been developed for the conversion of primary, secondary, and tertiary alcohols, and phenol, into the corresponding esters at room temperature. The method uses a titanium(III) species generated from a substoichiometric amount of titanocene dichloride together with manganese(0) as a reductant, as well as methylene diiodide. It involves a transesterification from an ethyl ester, or a reaction with an acyl chloride. A radical mechanism is proposed for these transformations.
Synthesis of Fatty Acid Ester by Corynebacterium sp. S-401
Seo, Chull Won,Yamada, Yasuhiro,Okada, Hirosuke
, p. 405 - 410 (2007/10/02)
Resting cells and acetone-dried cells of Corynebacterium sp.S-401 catalyzed the fatty acid ester synthesis of various alcohols and fatty acids.These reactions were carried out in phosphate buffer and/or organic solvents.In some cases synthetic reactions of esters in nonpolar solvents, such as n-hexane and benzene, gave better results compared with those obtained in phosphate buffer.
