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3-(Carboxymethylamino)propanoic acid, also known as CMPA, is a chemical compound with a molecular formula of C6H11NO4. It is a derivative of amino acids and is commonly used as a chelating agent in various applications, such as in the food and pharmaceutical industries. CMPA has the ability to bind and remove metal ions, making it useful for stabilizing products and preventing oxidation. It is also used in the production of certain drugs and as a component in cleaning products. CMPA is considered to be safe for consumption and has a wide range of industrial uses.

505-72-6

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505-72-6 Usage

Uses

Used in Food Industry:
3-(Carboxymethylamino)propanoic acid is used as a chelating agent for stabilizing food products and preventing oxidation.
Used in Pharmaceutical Industry:
3-(Carboxymethylamino)propanoic acid is used as a chelating agent for stabilizing pharmaceutical products and preventing oxidation.
Used in Drug Production:
3-(Carboxymethylamino)propanoic acid is used as a component in the production of certain drugs.
Used in Cleaning Products:
3-(Carboxymethylamino)propanoic acid is used as a component in cleaning products for its ability to bind and remove metal ions.

Check Digit Verification of cas no

The CAS Registry Mumber 505-72-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 505-72:
(5*5)+(4*0)+(3*5)+(2*7)+(1*2)=56
56 % 10 = 6
So 505-72-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NO4/c7-4(8)1-2-6-3-5(9)10/h6H,1-3H2,(H,7,8)(H,9,10)

505-72-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-((carboxymethyl)amino)propanoic acid

1.2 Other means of identification

Product number -
Other names Benzamidino-essigsaeure

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:505-72-6 SDS

505-72-6Relevant academic research and scientific papers

DERIVATIVES OF DOLASTATIN 10 AND USES THEREOF

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Page/Page column 26, (2016/12/22)

Derivatives of dolastatin 10 and uses thereof, the structures of which are shown as formula I, II, III and IV are provided.

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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