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5-methyl-2-(1-methylethyl)phenyl palmitate, also known as 2-isopropyltoluene palmitate, is a chemical compound derived from the esterification of 2-isopropyltoluene (also known as 2-methyl-4-(1-methylethyl)benzene) and palmitic acid. This organic compound is characterized by its molecular formula C21H34O2 and a molecular weight of 314.49 g/mol. It is a colorless to pale yellow liquid with a mild, pleasant odor. This ester is commonly used in the fragrance industry as a fixative and in the formulation of various cosmetic and personal care products due to its ability to stabilize and prolong the scent of other fragrance components. Additionally, it may have potential applications in the pharmaceutical and chemical industries.

6550-46-5

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6550-46-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6550-46-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,5 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6550-46:
(6*6)+(5*5)+(4*5)+(3*0)+(2*4)+(1*6)=95
95 % 10 = 5
So 6550-46-5 is a valid CAS Registry Number.
InChI:InChI=1/C26H44O2/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-26(27)28-25-21-23(4)19-20-24(25)22(2)3/h19-22H,5-18H2,1-4H3

6550-46-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-methyl-2-propan-2-ylphenyl) hexadecanoate

1.2 Other means of identification

Product number -
Other names 2-isopropyl-5-methylphenyl palmitate

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:6550-46-5 SDS

6550-46-5Downstream Products

6550-46-5Relevant academic research and scientific papers

Synthesis, antimicrobial activity and in silico studies on thymol esters

Lazarevi?, Jelena,Kolarevi?, Ana,Dordevi?, Aleksandra,Stojanovi?, Gordana,?melcerovi?, Andrija,Ciuffreda, Pierangela,Santaniello, Enzo

, p. 603 - 612 (2017/09/11)

Derivatisation of parent structure in terpenoids often results in enhancement of biological activity of newly obtained compounds. Thymol, a naturally occurring phenol biosynthesized through the terpene pathway, is a well known biocide with strong antimicrobial attributes and diverse therapeutic activities. We have aimed our study on a single modification of phenolic functionality in thymol in order to obtain a small focused library of twenty thymyl esters, ten of which were new compounds. All compounds were involved in in vitro antimicrobial testing. Another important aspect of current study was implementation of in silico calculation of physico-chemical, pharmacokinetic and toxicological properties, which could be helpful by giving an additional guidance in further research.

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