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Key Documents

A1506

Sigma-Aldrich

Anthranilic acid

Synonym(s):

2-AA, 2-Aminobenzoic acid

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About This Item

Linear Formula:
2-(H2N)C6H4CO2H
CAS Number:
Molecular Weight:
137.14
Beilstein/REAXYS Number:
471803
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:

vapor density

4.7 (vs air)

form

solid

mp

144-148 °C (lit.)

solubility

ethanol: soluble, clear to slightly hazy

SMILES string

Nc1ccccc1C(O)=O

InChI

1S/C7H7NO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4H,8H2,(H,9,10)

InChI key

RWZYAGGXGHYGMB-UHFFFAOYSA-N

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Application

Used for non-selective, efficient fluorescent labeling of glycans.

Replaced by

Product No.
Description
Pricing

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

302.0 °F - closed cup

flash_point_c

150 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Sangram S Kale et al.
Organic & biomolecular chemistry, 10(42), 8426-8433 (2012-09-25)
Structural modulation of Ant-Pro (anthranilic acid-proline) oligomers has been carried out by chirality alteration of the proline residues. The results suggest that the chirality altered oligomers show well-defined helical conformation featuring nine-membered hydrogen bonding interactions - without compromising conformational rigidity.
S Ahmad
Drug metabolism reviews, 10(1), 1-14 (1979-01-01)
Research in recent years has considerably enhanced our understanding of the membrane-bound cytochrome P-450-catalyzed biotransformations in organisms. A remarkable similarity has become apparent between diversified animal groups with respect to the components and functional roles of the cytochrome P-450 systems.
Li Gu et al.
The Analyst, 138(18), 5461-5469 (2013-07-26)
In this work, we report a competitive sensor performing "double recognition" for the specific capture of dopamine (DA) with the combination of boronic acid functional groups and molecularly imprinted cavities based on poly(aniline-co-anthranilic acid) (PANANA) as the support material. This
Stuart W Haynes et al.
Journal of the American Chemical Society, 134(42), 17444-17447 (2012-10-04)
Members of the asperlicin family of fungal metabolites produced by Aspergillus alliaceus are known potent CCK(A) antagonists. Herein, we report the identification of the gene cluster responsible for directing their biosynthesis. We validate and probe the pathway by genetic manipulation
W Spivak et al.
The Biochemical journal, 225(3), 787-805 (1985-02-01)
We describe a facile and sensitive reverse-phase h.p.l.c. method for analytical separation of biliary bile pigments and direct quantification of unconjugated bilirubin (UCB) and its monoglucuronide (BMG) and diglucuronide (BDG) conjugates in bile. The method can be 'scaled up' for

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