ChemicalBook > Product Catalog >Flavors and fragrances >Synthetic fragrances >Carboxylic acids and esters >Aromatic carboxylic acid ester >OCTYL ISOBUTYRATE

OCTYL ISOBUTYRATE

OCTYL ISOBUTYRATE Structure
CAS No.
109-15-9
Chemical Name:
OCTYL ISOBUTYRATE
Synonyms
ent24265;FEMA 2808;ENT 24265;Octylisobutyrat;OCLyl Isobutyrate;OCTYL ISOBUTYRATE;octyl isobutanoate;N OCTYL ISOBUTYRATE;CAPRYLYL ISOBUTYRATE;octyl2-methylpropanoate
CBNumber:
CB3152887
Molecular Formula:
C12H24O2
Molecular Weight:
200.32
MOL File:
109-15-9.mol
Modify Date:
2023/5/25 18:01:05

OCTYL ISOBUTYRATE Properties

Melting point -56°C (estimate)
Boiling point 245 °C(lit.)
Density 0.856 g/mL at 25 °C(lit.)
refractive index n20/D 1.421(lit.)
FEMA 2808 | OCTYL ISOBUTYRATE
Flash point 206 °F
color A colourless liquid.
Odor at 100.00 %. oily green waxy soapy clean fruity creamy
Odor Type waxy
JECFA Number 192
LogP 4.78
EPA Substance Registry System Propanoic acid, 2-methyl-, octyl ester (109-15-9)

SAFETY

Risk and Safety Statements

WGK Germany  2
RTECS  UA2466375
Toxicity Both the acute oral LD50 in rats and the acute dermal LD50 in rabbits exceeded 5 g/kg (Levenstein, 1974).

OCTYL ISOBUTYRATE Chemical Properties,Uses,Production

Description

Octyl isobutyrate has a fruity, fatty fragrance with a soft and humid undertone reminiscent of parsley and fern root with a sweet flavor suggestive of grape. May be prepared by esterification of n-octanol with isobutyric acid.

Chemical Properties

Octyl isobutyrate has a fruity, fatty fragrance with a soft and humid undertone reminiscent of parsley and fern root. It has a sweet flavor suggestive of grape.

Occurrence

Reported found among the volatile components of hop. Also reported found in grapefruit juice and babaco fruit (Carica pentagona Heilborn).

Uses

Octyl isobutyrate is used in imitation Pistacio, Grape, Melon, Peach, Citrus complexes, fruit blends, wine and Liqueur flavors, ect. The concentration is normally about 2 to 4 ppm in the finished product.

Preparation

Esterification of n-octanol with isobutyric acid.

Metabolism

Isobutyrates are hydrolysed to materials that are either normally in the diet or readily converted to such materials (Fassett, 1963a). Isobutyric acid occurs normally in the metabolism of valine, being converted to a propionyl group and entering into the glycogenic process (Fassett, 1963b). π-Octanol is largely oxidized in vivo; about 10% is excreted conjugated with glucuronic acid in rabbits. Isomeric octanols may be more highly conjugated; they may also be oxidized to the ketone or may be excreted unchanged (Williams, 1959).

OCTYL ISOBUTYRATE Preparation Products And Raw materials

Raw materials

Preparation Products

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OCLyl Isobutyrate N-OCTYL 2-METHYLPROPANOATE N OCTYL ISOBUTYRATE OCTYL ISOBUTYRATE OCTYL ISOBUTYRATE 98+% FCC Octylisobutyrat Propanoic acid, 2-methyl-, octyl ester、2-methyl-propanoic aci acetyl ester、acetyl 2-methylpropanoate、ent 24265、isobutyric acid, octyl ester、n-octyl isobutyrate、octyl 2-methylpropanoate CAPRYLYL ISOBUTYRATE FEMA 2808 2-methyl-propanoicaciacetylester 2-methyl-propanoicacioctylester 2-Methyl-propionicacidoctylester isobutyricacid,octylester Isobutyricacidoctylester octyl isobutanoate octyl2-methylpropanoate Propanoic acid, 2-methyl-, octyl ester Propanoicacid,2-methyl-,octylester Octyl-2-methylpropionate Isobutyric acid, octyl ester ent24265 ENT 24265 acetyl2-methylpropanoate 2-Methyl-Propanoic Acid Octyl Ester Octyl Isobutyrate USP/EP/BP TIANFUCHEM--High purity 109-15-9 OCTYL ISOBUTYRATE 109-15-9 CH32CHCO2CH27CH3 Alphabetical Listings Flavors and Fragrances O-P