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Merck
CN

A12658

N-Acetylanthranilic acid

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

Key Documents

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Product Name

N-Acetylanthranilic acid, 99%

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

SMILES string

CC(=O)Nc1ccccc1C(O)=O

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

Quality Level

100

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pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

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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Certificates of Analysis (COA)

Lot/Batch Number
STBB7816V
STBB7816
S90609
13912TW
05228BN

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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
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
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
Jörg Overhage et al.
Microbiology (Reading, England), 151(Pt 2), 491-500 (2005-02-09)
Arthrobacter nitroguajacolicus Rü61a, which utilizes quinaldine as sole source of carbon and energy, was shown to contain a conjugative linear plasmid of approximately 110 kb, named pAL1. It exhibits similarities with other linear plasmids from Actinomycetales in that it has
Christine Müller et al.
Applied and environmental microbiology, 80(23), 7266-7274 (2014-09-23)
A bacterial strain, which based on the sequences of its 16S rRNA, gyrB, catA, and qsdA genes, was identified as a Rhodococcus sp. closely related to Rhodococcus erythropolis, was isolated from soil by enrichment on the Pseudomonas quinolone signal [PQS;

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