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38300-04-8

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38300-04-8 Usage

General Description

4-N-decylbenzoic acid is an organic compound with the chemical formula C16H26O2. It is a white solid that is insoluble in water and has a very low solubility in most organic solvents. This chemical is a member of the benzoic acid family and is often used as an intermediate in the synthesis of other chemicals. It is also used as a surfactant, a wetting agent, and a dispersing agent in various industrial applications. Additionally, 4-N-decylbenzoic acid has potential uses in pharmaceuticals and personal care products due to its antimicrobial and skin conditioning properties.

Check Digit Verification of cas no

The CAS Registry Mumber 38300-04-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,3,0 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 38300-04:
(7*3)+(6*8)+(5*3)+(4*0)+(3*0)+(2*0)+(1*4)=88
88 % 10 = 8
So 38300-04-8 is a valid CAS Registry Number.
InChI:InChI=1/C17H26O2/c1-2-3-4-5-6-7-8-9-10-15-11-13-16(14-12-15)17(18)19/h11-14H,2-10H2,1H3,(H,18,19)

38300-04-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Decylbenzoic acid

1.2 Other means of identification

Product number -
Other names 4-decylbenzoic acid

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:38300-04-8 SDS

38300-04-8Relevant articles and documents

Nickel-butadiene catalytic system for the cross-coupling of bromoalkanoic acids with alkyl grignard reagents: A practical and versatile method for preparing fatty acids

Iwasaki, Takanori,Higashikawa, Kiyokazu,Reddy, Vutukuri P.,Ho, Willbe W. S.,Fujimoto, Yukari,Fukase, Koichi,Terao, Jun,Kuniyasu, Hitoshi,Kambe, Nobuaki

supporting information, p. 2956 - 2960 (2013/03/28)

The knights who say Ni: A practical and convenient synthetic route to fatty acids involves the Ni-catalyzed alkyl-alkyl cross-coupling of bromoalkanoic acids and alkyl Grignard reagents in the presence of 1,3-butadiene as an additive (see scheme). Copyright

Rigid amphiphiles for membrane protein manipulation

McQuade, D. Tyler,Quinn, Mariah A.,Yu, Seungju M.,Polans, Arthur S.,Krebs, Mark P.,Gellman, Samuel H.

, p. 758 - 761 (2007/10/03)

The two nonhomologous membrane proteins bacteriorhodopsin and bovine rhodopsin can be extracted from their native membranes by the rigid tripod amphiphile 1. Both proteins are maintained in a stable, soluble form, which is a prerequisite for crystallization. This new class of amphiphiles can be easily modified and could prove to be very useful for membrane protein manipulation.

Arylhydroxamates useful as antiallergy agents

-

, (2008/06/13)

Arylhydroxamates are provided having the structure STR1 wherein R1 is hydrogen, lower alkyl, aryl, lower alkenyl, cycloalkenyl, aralkyl, or STR2 wherein n is 1 to 4 and X is hydroxy, alkoxy, amino, C1 -C4 -alkylamino or C1 -C4 -dialkylamino. R2 is hydrogen or lower alkyl; and R3 is C1 -C20 alkyl or C3 -C20 alkenyl, aryl, aryl-alkyl, cycloalkyl, aryl-alkenyl, lower alkoxy, lower alkenyloxy, aryl-alkoxy or cycloalkyloxy. These compound are useful as inhibitors of Δ5 -lipoxygenase and as such are useful as antiallergy agents.

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