Welcome to LookChem.com Sign In|Join Free
  • or
Glycine linoleamide is a chemical compound that combines glycine, an amino acid, with linoleic acid, an essential fatty acid. It is recognized for its moisturizing, nourishing, and skin barrier-improving properties, as well as its emollient effects that contribute to skin softness and smoothness. Furthermore, glycine linoleamide exhibits anti-inflammatory and antioxidant capabilities, making it a beneficial ingredient in skincare formulations designed to enhance skin health and appearance.

2764-03-6

Post Buying Request

2764-03-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

2764-03-6 Usage

Uses

Used in Cosmetic and Personal Care Industry:
Glycine linoleamide is used as an emollient and skin conditioning agent for its ability to moisturize and nourish the skin, improving the skin's barrier function. It is particularly effective in softening and smoothing the skin, making it a common ingredient in moisturizers, lotions, and other skincare products.
Used in Skincare Formulations:
Glycine linoleamide is used as an active ingredient for its anti-inflammatory and antioxidant effects, contributing to the improvement of skin health and appearance. Its inclusion in skincare products helps to soothe inflammation and protect the skin from oxidative stress, promoting a healthier and more youthful complexion.

Check Digit Verification of cas no

The CAS Registry Mumber 2764-03-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,6 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2764-03:
(6*2)+(5*7)+(4*6)+(3*4)+(2*0)+(1*3)=86
86 % 10 = 6
So 2764-03-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H35NO3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-19(22)21-18-20(23)24/h6-7,9-10H,2-5,8,11-18H2,1H3,(H,21,22)(H,23,24)/b7-6-,10-9-

2764-03-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Linoleoyl Glycine

1.2 Other means of identification

Product number -
Other names Linoleoyl-glycin

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:2764-03-6 SDS

2764-03-6Downstream Products

2764-03-6Relevant academic research and scientific papers

Preparation method and application of compound with beta amyloid protein resisting activity

-

, (2019/12/29)

The present invention provides a compound represented by formula I, or a pharmaceutically acceptable salt thereof. The invention also provides a preparation method of the compound. Experimental results show that the compound is suitable for industrial pro

Improvements in or Relating to Organic Compounds

-

, (2016/08/17)

A stock solution comprising a compound of formula (I) Wherein R1 together with the carbonyl group to which it is attached is a residue of a carboxylic acid, and NR2R3, in which R3 is H or together with R2 and the N-atom to which they are attached, a 5-membered ring, is a residue of an amino acid, in particular a proteinogenic amino acid, ornithine, gamma-aminobutyric acid or beta alanine, or a 1-amino cycloalkyl carboxylic acid.

Evaluation of endogenous fatty acid amides and their synthetic analogues as potential anti-inflammatory leads

Dang, Hung The,Kang, Gyeoung Jin,Yoo, Eun Sook,Hong, Jongki,Choi, Jae Sue,Kim, Hyung Sik,Chung, Hae Young,Jung, Jee H.

experimental part, p. 1520 - 1527 (2011/03/23)

A series of endogenous fatty acid amides and their analogues (1-78) were prepared, and their inhibitory effects on pro-inflammatory mediators (NO, IL-1β, IL-6, and TNF-α) in LPS-activated RAW264.7 cells were evaluated. Their inhibitory activity on the pro-inflammatory chemokine MDC in IFN-γ-activated HaCaT cells was also examined. The results showed that the activity is strongly dependent on the nature of the fatty acid part of the molecules. As expected, the amides derived from enone fatty acids showed significant activity and were more active than those derived from other types of fatty acids. A variation of the amine headgroup also altered bioactivity profile remarkably, possibly by modulating cell permeability. Regarding the amine part of the molecules, N-acyl dopamines exhibited the most potent activity (IC50 ~2 μM). This is the first report of the inhibitory activity of endogenous fatty acid amides and their analogues on the production of nitric oxide, cytokines (IL-1β, IL-6, and TNF-α) and the chemokine MDC. This study suggests that the enone fatty acid-derived amides (such as N-acyl ethanolamines and N-acyl amino acids) and N-acyl dopamines may be potential anti-inflammatory leads.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 2764-03-6