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612-42-0

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612-42-0 Structure

612-42-0 Structure
IdentificationMore
[Name]

N-(2-CARBOXYPHENYL)GLYCINE
[CAS]

612-42-0
[Synonyms]

2-(CARBOXYMETHYL-AMINO)-BENZOIC ACID
AKOS AU36-M366
AKOS BBS-00007771
N-(2-CARBOXYPHENYL)GLYCINE
N-(CARBOXYMETHYL)ANTHRANILIC ACID
N-(CARBOXYPHENYL)GLYCINE
N-PHENYLGLYCINE-O-CARBOXYLIC ACID
TIMTEC-BB SBB006542
2-[(carboxymethyl)amino]-benzoicaci
anthranilidoacetic acid
(2-carboxyphenyl)glycine
[(2-Carboxyphenyl)amino]acetic acid
2-[(2-Oxo-2-hydroxyethyl)amino]benzoic acid
Anthranilinoacetic acid
[EINECS(EC#)]

210-311-5
[Molecular Formula]

C9H9NO4
[MDL Number]

MFCD00020445
[Molecular Weight]

195.17
[MOL File]

612-42-0.mol
Chemical PropertiesBack Directory
[Appearance]

light yellow to yellow crystalline powder
[Melting point ]

218 °C (dec.)(lit.)
[Boiling point ]

218°C
[density ]

1.472
[refractive index ]

1.5700 (estimate)
[Fp ]

218°C/
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

Crystalline Powder
[pka]

3?+-.0.36(Predicted)
[color ]

Light yellow to yellow
[CAS DataBase Reference]

612-42-0(CAS DataBase Reference)
[EPA Substance Registry System]

Benzoic acid, 2-[(carboxymethyl)amino]- (612-42-0)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection .
[WGK Germany ]

3
[TSCA ]

Yes
[REACH Registrations]

Active
[HazardClass ]

IRRITANT
[HS Code ]

29224985
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Anthranilic acid
[Preparation Products]

N-Acetyl-3-hydroxyindole-->INDOXYL ACETATE-->Indigo
Hazard InformationBack Directory
[Chemical Properties]

light yellow to yellow crystalline powder
[Uses]

2-((Carboxymethyl)amino)benzoic acid is a Glycine (HY-Y0966) derivative[1].
[Purification Methods]

Crystallise the acid from hot water (charcoal). It forms complexes with Cu2+, Zn2+, Cd2+, Co2+ and Ni2+ in aqueous dioxane. [Roileanu et al. Rev Roum Chim 12 105 1967, Aldrich library of 13C, 1H FTNMR Spectra, NMR 2 1181A, Beilstein 14 H 348, 14 I 544, 14 II 225, 14 III 938.]
[References]

[1] Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144. DOI:10.1080/10408398.2012.708368
Spectrum DetailBack Directory
[Spectrum Detail]

N-(2-CARBOXYPHENYL)GLYCINE(612-42-0)MS
N-(2-CARBOXYPHENYL)GLYCINE(612-42-0)1HNMR
N-(2-CARBOXYPHENYL)GLYCINE(612-42-0)IR1
N-(2-CARBOXYPHENYL)GLYCINE(612-42-0)IR2
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

N-(2-Carboxyphenyl)glycine, 97%(612-42-0)
[Alfa Aesar]

N-(2-Carboxyphenyl)glycine, 97%(612-42-0)
[Sigma Aldrich]

612-42-0(sigmaaldrich)
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