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Alanine, N-(carboxymethyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 106327-05-3 Structure
  • Basic information

    1. Product Name: Alanine, N-(carboxymethyl)- (9CI)
    2. Synonyms: Alanine, N-(carboxymethyl)- (9CI)
    3. CAS NO:106327-05-3
    4. Molecular Formula: C5H9NO4
    5. Molecular Weight: 147.12926
    6. EINECS: N/A
    7. Product Categories: GLYCINESCAFFOLD
    8. Mol File: 106327-05-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Alanine, N-(carboxymethyl)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Alanine, N-(carboxymethyl)- (9CI)(106327-05-3)
    11. EPA Substance Registry System: Alanine, N-(carboxymethyl)- (9CI)(106327-05-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 106327-05-3(Hazardous Substances Data)

106327-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106327-05-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,3,2 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 106327-05:
(8*1)+(7*0)+(6*6)+(5*3)+(4*2)+(3*7)+(2*0)+(1*5)=93
93 % 10 = 3
So 106327-05-3 is a valid CAS Registry Number.

106327-05-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Acide methyl-2 aza-3 pentanedioique-1,5

1.2 Other means of identification

Product number -
Other names N-carboxymethyl-DL-alanine

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:106327-05-3 SDS

106327-05-3Downstream Products

106327-05-3Relevant articles and documents

SYNTHESE D'AMINODIACIDES

Garrigues, Bernard

, p. 1151 - 1156 (2007/10/02)

A general method for the synthesis of a new aminodiacids (4) by aminodiesters (3) hydrolysis is presented.

Mass Spectra of Butyl Esters and N-Trifluoroacetyl Butyl Esters of Some Iminodicarboxylic Acids upon Electron Impact

Kawashiro, Katsuhiro,Morimoto, Shiro,Yoshida, Hideyuki

, p. 1097 - 1103 (2007/10/02)

Mass spectra (electron impact at 20 eV) of butyl esters and N-trifluoroacetyl (TFA) butyl esters of some iminodicarboxylic acids (IDCAs) were determined by gas chromatography-mass spectrometry.The IDCAs included iminodiacetic acid (1), 2-(carboxymethylamino)propionic acid (2), 3-(carboxymethylamino)propionic acid (3), 2,2'-iminodipropionic acid (4), 2,3'-iminodipropionic acid (5), 3,3'-iminodipropionic acid (6), N-methylaminodiacetic acid (7), and nitrilotriacetic acid (8).The mass spectra of the butyl ester derivatives are simple, exhibiting the corresponding molecular (M+) ions with the exception of 5.The α,α'-IDCAs (1, 2, 4, 7, and 8) are characterized by M+, M -101 (COOC4H9) (base peak), and M - 157 (COOC4H9 + C4H8) ions.The β,β'-IDCA (6) is characterized by a more complex spectrum with M+, M - 73 (OC4H9), M - 115 (CH2COOC4H9) (base peak), M - 129 (OC4H9 + C4H9), and M - 171 (CH2COOC4H9 + C4H9) ions.The α,β'-IDCAs (3 and 5) in general show spectra in which both ions characteristic of α,α'- and β,β'-IDCAs are observed.The addition of TFA to the imino nitrogens of 1 - 6 increases complexity of the resulting spectra.In these instances, although M+ ions are usually present, neither M - 101 nor 115 ions are base peaks.The fragmentation pathways of these two volatile derivatives of the IDCAs upon electron impact are discussed.

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