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7505-12-6

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7505-12-6 Usage

General Description

Triaconatanoic acid ethyl ester, also known as ethyl triacontanoate, is a chemical compound belonging to the class of esters. It is derived from the reaction between triacontanoic acid and ethanol. This colorless, odorless liquid is commonly used in the flavor and fragrance industry as a flavoring agent and as a scent in perfumes and cosmetics. Additionally, it is utilized as a lubricant and an ingredient in industrial coatings. Triacontanoic acid ethyl ester is also found in some natural sources such as certain plants and flowers. It has been shown to have low toxicity and is generally considered safe for use in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 7505-12-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,0 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7505-12:
(6*7)+(5*5)+(4*0)+(3*5)+(2*1)+(1*2)=86
86 % 10 = 6
So 7505-12-6 is a valid CAS Registry Number.
InChI:InChI=1/C32H64O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-30-31-32(33)34-4-2/h3-31H2,1-2H3

7505-12-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl triacontanoate

1.2 Other means of identification

Product number -
Other names Ethyl tricontanoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:7505-12-6 SDS

7505-12-6Relevant articles and documents

NEW SYNTHESIS OF 1-TRIACONTANOL

Bhalerao, U. T.,Rao, Jagadishwar S.,Tilak, B. D.

, p. 5439 - 5440 (2007/10/02)

Succinic anhydride and behenic acid have been used to attach C4 and C22 carbon chains on to 2 and 5 positions of thiophene through two alternate acylation sequences.Raney nickel desulphurization to the 2,5-disubstituted thiophene yielded triacontanoic acid esters which on LAH reduction gave 1-triacontanol.

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