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A12658

N-Acetylanthranilic acid

Name: <I>N</I>-Acetylanthranilic acid
Brand: ALDRICH

99%

Synonym(s):

2-Acetamidobenzoic acid

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About This Item

Linear Formula:

(CH₃CONH)C₆H₄CO₂H

CAS Number:

89-52-1

Molecular Weight:

179.17

NACRES:

NA.22

PubChem Substance ID:

24890519

eCl@ss:

32160406

UNSPSC Code:

12352200

EC Number:

201-914-4

MDL number:

MFCD00002423

Beilstein/REAXYS Number:

880371

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Properties

Quality Level

100

assay

99%

form

powder

reaction suitability

reaction type: solution phase peptide synthesis

color

off-white to tan

mp

184-187 °C (lit.)

application(s)

peptide synthesis

SMILES string

CC(=O)Nc1ccccc1C(O)=O

InChI

1S/C9H9NO3/c1-6(11)10-8-5-3-2-4-7(8)9(12)13/h2-5H,1H3,(H,10,11)(H,12,13)

InChI key

QSACCXVHEVWNMX-UHFFFAOYSA-N

Description

pictograms

GHS07

signalword

Warning

hcodes

H302

pcodes

P264 - P270 - P301 + P312 + P330 - P501

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

监管及禁止进口产品

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Microbial metabolism of quinoline and related compounds. VI. Degradation of quinaldine by Arthrobacter sp.

H K Hund et al.

Biological chemistry Hoppe-Seyler, 371(10), 1005-1008 (1990-10-01)

Quinaldine catabolism was investigated with the bacterial strain Arthrobacter sp., which is able to grow aerobically in a mineral salt medium with quinaldine as sole source of carbon, nitrogen and energy. The following degradation products of quinaldine were isolated from

Mechanisms of photoinduced electron transfer reactions of lappaconitine with aromatic amino acids. Time-resolved CIDNP study.

Nikolai E Polyakov et al.

Organic & biomolecular chemistry, 3(5), 881-885 (2005-02-26)

CIDNP techniques were applied to the investigation of the elementary mechanism of photoinduced interaction between anti-arrhythmic drug lappaconitine and amino acids tyrosine and tryptophan. It has been shown that the reactions involve the formation of lappaconitine radical anion. Lappaconitine radical

N-acetylanthranilate amidase from Arthrobacter nitroguajacolicus Rü61a, an alpha/beta-hydrolase-fold protein active towards aryl-acylamides and -esters, and properties of its cysteine-deficient variant.

Stephan Kolkenbrock et al.

Journal of bacteriology, 188(24), 8430-8440 (2006-10-17)

N-acetylanthranilate amidase (Amq), a 32.8-kDa monomeric amide hydrolase, is involved in quinaldine degradation by Arthrobacter nitroguajacolicus Rü61a. Sequence analysis and secondary structure predictions indicated that Amq is related to carboxylesterases and belongs to the alpha/beta-hydrolase-fold superfamily of enzymes; inactivation of

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Global Trade Item Number

SKU	GTIN
A12658-25G	04061832596884