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2601-90-3

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2601-90-3 Usage

Description

N-Oleoyl glycine is a putative substrate for peptidyl glycine α-amidating enzyme in the biosynthesis of oleoyl amide.

Definition

ChEBI: A fatty acid derivative that is the 9Z-octadecenoyl derivative of glycine.

Check Digit Verification of cas no

The CAS Registry Mumber 2601-90-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,0 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2601-90:
(6*2)+(5*6)+(4*0)+(3*1)+(2*9)+(1*0)=63
63 % 10 = 3
So 2601-90-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H37NO3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-19(22)21-18-20(23)24/h9-10H,2-8,11-18H2,1H3,(H,21,22)(H,23,24)/b10-9-

2601-90-3 Well-known Company Product Price

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  • Sigma

  • (O9762)  N-Oleoylglycine  ≥98%

  • 2601-90-3

  • O9762-10MG

  • 512.46CNY

  • Detail

2601-90-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Oleoylglycine

1.2 Other means of identification

Product number -
Other names N-(1-Oxo-9-octadecenyl)-(Z)-glycine

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:2601-90-3 SDS

2601-90-3Relevant articles and documents

Thixotropic stiff hydrogels from a new class of oleoyl-d-glucamine-based low-molecular-weight gelators

Ohsedo, Yutaka,Oono, Masashi,Saruhashi, Kowichiro,Watanabe, Hisayuki,Miyamoto, Nobuyoshi

, p. 41686 - 41692 (2017)

A series of new compounds comprising oleoyl, amino acid and d-glucamine moieties were synthesised using mild reaction conditions, and their hydrogelation ability was evaluated. The gels exhibited improved stiffness and thixotropic properties dependent on the chemical structure of the amino acid linker and the number of potential hydrogen bonding sites.

Cosmetic composition for eliminating or adsorbing particulate matter comprising peptide complex as effective component

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Paragraph 0031-0032; 0034-0046; 0063; 0065, (2020/03/17)

The present invention relates to a cosmetic composition for removing or adsorbing fine dust, containing a fatty acid-amino acid complex or a fatty acid-oligopeptide complex as an active ingredient. The complex of the present invention has an excellent effect of removing fine dust without skin toxicity, and thus can be effectively used as a composition for preventing or treating various diseases caused by fine dust.COPYRIGHT KIPO 2020

Method for synthesizing fatty acyl glycocoll

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Paragraph 0031; 0032, (2017/01/02)

The invention discloses a method for synthesizing fatty acyl glycocoll. The method comprises the steps that an oxidant, a catalyst promoter and an alkali solution are mixed into an aqueous solution, the aqueous solution is added into an organic solvent system formed by mixing fatty acid monoethanolamide and a catalyst, a reaction is carried out for 0.5-3 h under the condition of maintaining the pH of the whole mixed system to be 6.0-12.0 and the temperature to be 20-40 DEG C, then a reaction is carried out for 0.5-2 h under stirring, and a product containing fatty acyl glycocoll is obtained. According to the method for synthesizing fatty acyl glycocoll, the reaction speed and the product yield are high, the reaction condition is mild and easy to control, and the method for synthesizing fatty acyl glycocoll is efficient, conforms to environment-friendly chemistry and is capable of facilitating industrialized production.

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