ChemicalBook > Product Catalog >Flavors and fragrances >Synthetic fragrances >Carboxylic acids and esters >Aromatic carboxylic acid ester >ALLYLCYCLOHEXANE ACETATE

ALLYLCYCLOHEXANE ACETATE

ALLYLCYCLOHEXANE ACETATE Structure
CAS No.
4728-82-9
Chemical Name:
ALLYLCYCLOHEXANE ACETATE
Synonyms
ALLYLCYCLOHEXYLACETATE;ALLYLCYCLOHEXANE ACETATE;Cyclohexylacetic acid allyl ester;ALLYLCYCLOHEXANE ACETATE USP/EP/BP;Cyclohexaneacetic acid, 2-propenyl ester;Cyclohexaneacetic acid, 2-propen-1-yl ester
CBNumber:
CB7477580
Molecular Formula:
C11H18O2
Molecular Weight:
182.26
MOL File:
4728-82-9.mol
Modify Date:
2024/6/5 9:38:15

ALLYLCYCLOHEXANE ACETATE Properties

Boiling point 275.67°C (rough estimate)
Density 0.9813 (rough estimate)
refractive index 1.4614 (estimate)
FEMA 2023 | ALLYL CYCLOHEXANEACETATE
color A colourless liquid.
Odor at 100.00 %. sweet ripe fruity pineapple green peach apricot
Odor Type fruity
JECFA Number 12
LogP 3.59
EPA Substance Registry System Cyclohexaneacetic acid, 2-propenyl ester (4728-82-9)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H312-H302-H319
Precautionary statements  P264-P270-P301+P312-P330-P501-P280-P302+P352-P312-P322-P363-P501-P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
Toxicity The acute oral LD50 value in rats was reported as 0.90 g/kg (0.56-1.24 g/kg) (Moreno, 1974) and the acute dermal LD50 value in rabbits as 1.25 g/kg (0.35-2.15 g/kg) (Moreno, 1974).

ALLYLCYCLOHEXANE ACETATE Chemical Properties,Uses,Production

Chemical Properties

Colorless liquid, almost insoluble in water, miscible with alcohol, essential oils and flavor chemicals, perfume materials, etc. Pronounced “mixed-fruity“ odor, sweet, lasting and less ethereal than the lower aliphatic acetates. The flavor is overall fruity (“tutti-frutti”) with some resemblance to Pineapple, Peach and Apricot.

Occurrence

Has apparently not been reported to occur in nature.

Preparation

By esterfication of cyclohexane, acetic acid and allyl alcohol in the presence of benzene

Metabolism

The hydrolysis of ester linkages in foreign compounds may be catalysed by many different esterases; most of these have a low degree of substrate specificity and they are to be found in all animals and bacteria (Parke, 1968). In the rat, allyl acetate and allyl alcohol are metabolized to 3-hydroxypropylmercapturic acid, which is excreted in the urine (Clapp, Kaye & Young, 1969). In dogs, cyclohexylacetic acid was not aromatized and was probably completely oxidized in the body by β-oxidation (Bernhard, 1937; Williams, 1959).

ALLYLCYCLOHEXANE ACETATE Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 12)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
Dideu Industries Group Limited +86-29-89586680 +86-15129568250 China 26165 58 Inquiry
ZHEJIANG JIUZHOU CHEM CO., LTD +86-0576225566889 +86-13454675544 China 19947 58 Inquiry
BOC Sciences 1-631-485-4226; 16314854226 United States 14059 65 Inquiry
Baoji Didu Pharmaceutical and Chemical Co., Ltd 029-61856358 15829046862 China 10011 58 Inquiry
TCI (Shanghai) Chemical Trading Co., Ltd. 021-021-61109150 China 31163 58 Inquiry
ChemSampCo, Inc. 609 656 2440 United States 3585 60 Inquiry
3B Scientific Corporation 847.281.9822 United States 6744 47 Inquiry
Shanghai wencai New Material Technology Co., Ltd. 15721586846 China 2796 58 Inquiry
Jiangyin Healthway International Trade Co., Ltd 86-510-86023169 United States 1006 58 Inquiry
Pyrazine Specialties, Inc. (404) 524-6744 United States 1265 30 Inquiry

4728-82-9(ALLYLCYCLOHEXANE ACETATE)Related Search:

Cyclohexaneacetic acid, 2-propenyl ester ALLYLCYCLOHEXYLACETATE ALLYLCYCLOHEXANE ACETATE Cyclohexylacetic acid allyl ester ALLYLCYCLOHEXANE ACETATE USP/EP/BP Cyclohexaneacetic acid, 2-propen-1-yl ester 4728-82-9