A12658

Sigma-Aldrich

N-Acetylanthranilic acid

99%

Synonym(s):
2-Acetamidobenzoic acid
Linear Formula:
(CH3CONH)C6H4CO2H
CAS Number:
Molecular Weight:
179.17
Beilstein/REAXYS Number:
880371
EC Number:
MDL number:
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

99%

form

powder

reaction suitability

reaction type: solution phase peptide synthesis

application(s)

peptide synthesis: suitable

color

off-white to tan

mp

184-187 °C (lit.)

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

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Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

hazcat

Acute Tox. 4 Oral

storage_class_code

13 - Non Combustible Solids

WGK Germany

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

Certificate of Analysis

Certificate of Origin

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...
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...
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...
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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