Welcome to LookChem.com Sign In|Join Free
  • or
Glycine, N-methyl-N-(1-oxohexadicyl), also known as N-methyl-N-(1-oxohexadecyl) glycine, is a chemical compound with the molecular formula C19H37NO3. It is a derivative of glycine, an amino acid, where the amino group is substituted with a long-chain aliphatic group (1-oxohexadecyl) and a methyl group. Glycine,N-methyl-N-(1-oxohexadicyl) is characterized by its amphiphilic nature, possessing both hydrophilic (polar) and hydrophobic (non-polar) properties, which can be useful in various applications such as surfactants, emulsifiers, and in the formulation of personal care products. The compound's structure allows it to interact with both water and oil, making it a potential candidate for applications where the manipulation of interfacial properties is required.

2421-33-2

Post Buying Request

2421-33-2 Suppliers

Recommended suppliers

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

2421-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2421-33-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,2 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2421-33:
(6*2)+(5*4)+(4*2)+(3*1)+(2*3)+(1*3)=52
52 % 10 = 2
So 2421-33-2 is a valid CAS Registry Number.

2421-33-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Sodium N-methyl-n-(1-oxohexadecyl)aminoacetate.Hydrochloride

1.2 Other means of identification

Product number -
Other names -

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:2421-33-2 SDS

2421-33-2Downstream Products

2421-33-2Relevant academic research and scientific papers

Use of n-acylamino acid compounds as texturing agents

-

, (2008/06/13)

Use of at least one compound of formula (I): in which R represents the characterizing chain of a saturated or unsaturated, linear or branched fatty acid, comprising from 16 to 22 carbon atoms, represents the characterizing chain or cyclic radical of an amino acid, R2represents a hydrogen atom or an alkyl radical comprising from 1 to 3 carbon atoms, or the topically acceptable salts thereof, as texturing agents, it being understood that the amino acid characterized by R1is not lysine, hydroxylysine or arginine. Novel compositions Application in cosmetics.

A comparative study on the surface activity and micellar behaviour of some N-acylamino acid based surfactants

George, Alex,Modi, Jayesh,Jain, Nirmesh,Bahadur, Pratap

, p. 985 - 992 (2007/10/03)

N-Hexadecanoyl derivatives of amino acids viz alanine, sarcosine, glycine, aspartic acid, glutamic acid and dioctanoyl derivative of lysine and their sodium salts have been synthesised and characterised spectrophotometrically and by elemental analysis. Activation energy for thermal decomposition of these surfactants has been obtained using thermogravimetric analysis. Studies on surface activity and micellization of these N-acylamino acid based surfactants using surface tension and dye-solubilization techniques reveal specific relationship between their structural characteristics and solution behaviour. The observed trend of CMC for these amphiphiles are explained in terms of varying hydrophobicity with changes in their molecular architecture. Dioctanoyllysinate displays high CMC value by virtue of two short C8-chains compared to the single and more hydrophobic C16-chain of the other surfactants. Hexadecanoylaspartate and glutamate, with their hydrophilicity enhanced by the presence of two carboxylate head groups, also display relatively higher CMCs. Solubilizing properties for these surfactants follow an order similar to that observed for their CMCs. Areas per molecule calculated indicate the influence of molecular structure on the packing of these surfactants at the air-water interface.

Vinyl carboxylate an acylating reagent for selective acylation of amines and diols

Chen,Chen,Chen,Wang

, p. 3583 - 3584 (2007/10/02)

Vinyl group of vinyl alkylate (C=2 or 16) and vinyl benzoate have been found to be a good leaving group in acylation of alcohols (40-50% yield) and amines (in 60-90% yield).

Melting Behaviour of Some Pure N-Acyl Amino Acids and Peptides

Iyer, Venkataraman N.,Sheth, Geeta N.,Subrahmanyam, V. V. R.

, p. 856 - 859 (2007/10/02)

Fifty three tlc pure N-acyl amino acids were synthesized by Schotten-Baumann reaction from glc pure odd and even chain fatty acids and chromatographycally homogeneous amino acids and a few N-acyl peptides were prepared through the carboxylic carbonic anhydride intermediates.The melting points are reported and discussed.

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 2421-33-2