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30673-38-2

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30673-38-2 Usage

Description

Isobutyl Decanoate, also known as isopentyl decanoate, is a decanoate ester derived from the formal condensation of the carboxy group of decanoic acid (capric acid) with the alcoholic hydroxy group of isobutanol. It is a colorless to pale yellow liquid with a fruity, pear-like odor and is commonly used in the fragrance and flavor industries.

Uses

Used in Fragrance Industry:
Isobutyl Decanoate is used as a fragrance ingredient for its ability to provide a fruity, pear-like aroma to various products. It is widely used in the formulation of perfumes, colognes, and other scented products due to its pleasant and distinctive scent.
Used in Flavor Industry:
Isobutyl Decanoate is used as a flavor ingredient for its fruity, pear-like taste, which can enhance the flavor profile of various food and beverage products. It is particularly useful in the creation of fruit-flavored products, such as candies, beverages, and desserts.
Used in Cosmetics and Personal Care Products:
Isobutyl Decanoate is used as an emollient, solvent, and fixative in the formulation of cosmetics and personal care products. Its ability to improve the texture and feel of products, as well as its capacity to help other ingredients blend more effectively, makes it a valuable component in the development of skincare, haircare, and other personal care products.
Used in the Pharmaceutical Industry:
Isobutyl Decanoate is used as a solvent and excipient in the pharmaceutical industry. Its properties allow it to help dissolve and stabilize active ingredients in medications, improving their overall effectiveness and bioavailability.

Synthesis Reference(s)

The Journal of Organic Chemistry, 51, p. 546, 1986 DOI: 10.1021/jo00354a030

Check Digit Verification of cas no

The CAS Registry Mumber 30673-38-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,6,7 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 30673-38:
(7*3)+(6*0)+(5*6)+(4*7)+(3*3)+(2*3)+(1*8)=102
102 % 10 = 2
So 30673-38-2 is a valid CAS Registry Number.

30673-38-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name isobutyl decanoate

1.2 Other means of identification

Product number -
Other names ISOBUTYL DECANOATE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:30673-38-2 SDS

30673-38-2Relevant articles and documents

Identification and synthesis of new sex-specific components of olive fruit fly (Bactrocera oleae) female rectal gland, through original Negishi reactions on supported catalysts

Fusini, Graziano,Barsanti, Davide,Angelici, Gaetano,Casotti, Gianluca,Canale, Angelo,Benelli, Giovanni,Lucchi, Andrea,Carpita, Adriano

supporting information, p. 4381 - 4389 (2018/07/21)

In the present study, eleven new sex-specific components extracted from female rectal gland of olive fruit flies were synthesized and identified. The quantitative determination of those components by GC and GC/EI-MS, at different moments of the insect life span, highlighted the growing trend of their secretion. While for the synthesis of saturated esters, conventional transesterification methods could be adopted, for the synthesis of unsaturated components, a Negishi cross-coupling between organozinc halides and (Z)-1-bromo-1-alkenes was developed. To the extent of our knowledge, this reaction represents the first example of supported-catalyst promoted Negishi coupling, between an alkylzinc reagent and an alkenyl halide.

A Simple and Efficient Esterification Method

Ming-Yi, Chen,Lee, Adam Shih-Yuan

, p. 103 - 108 (2007/10/03)

A convenient and practical esterification was realized and this reaction proceeded without a dehydrating reagent or water removal equipment. The synthesis of esters by reaction of carboxylic acids with various alcohols such as methyl, ethyl, isopropyl, isobutyl, allyl, benzyl, propargyl and decanyl alcohols were achieved with a catalytic amount of CBr4 under refluxing reaction condition.

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