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255300

Sigma-Aldrich

3-Aminosalicylic acid

97%, for peptide synthesis

Synonym(s):

3-Amino-2-hydroxybenzoic acid

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About This Item

Linear Formula:
H2NC6H3-2-(OH)CO2H
CAS Number:
570-23-0
Molecular Weight:
153.14
Beilstein:
2090427
EC Number:
209-328-0
MDL number:
MFCD00010299
UNSPSC Code:
12352106
PubChem Substance ID:
24855412
NACRES:
NA.22

product name

3-Aminosalicylic acid, 97%

Assay

97%

form

powder or crystals

reaction suitability

reaction type: solution phase peptide synthesis

mp

240 °C (dec.) (lit.)

application(s)

peptide synthesis

SMILES string

Nc1cccc(C(O)=O)c1O

InChI

1S/C7H7NO3/c8-5-3-1-2-4(6(5)9)7(10)11/h1-3,9H,8H2,(H,10,11)

InChI key

IQGMRVWUTCYCST-UHFFFAOYSA-N

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Application

3-Aminosalicylic acid is a building block that can be used to synthesize antimycin A3. It can also be used to synthesize 2-alkoxy-3-(arylaminomethylene)chroman-4-ones and 3-(aryliminomethyl)chromones by reacting with 3-formylchromones.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Synthesis and anticancer activity of polyhydroxylated 18-membered analogue of antimycin A 3
Arsianti A, et al.
Tetrahedron, 68(13), 2884-2891 (2012)
Reaction of 3-formylchromones with aromatic amino carboxylic acids.
Stankovicova H, et al.
Tetrahedron, 57(16), 3455-3464 (2001)
Ambareesh Kumar Singh et al.
Biosensors & bioelectronics, 74, 711-717 (2015-07-27)
A sensor for the determination of melphalan (mel) using 3-thiophene acetic acid (3-TAA) as functional monomer was fabricated by electropolymerization on gold surface. The polymeric film was formed on the surface of gold electrode as well as on gold-coated electrochemical
Kevin Guo et al.
Analytical chemistry, 81(10), 3919-3932 (2009-03-25)
We report a new quantitative metabolome profiling technique based on differential (12)C-/(13)C-isotope dansylation labeling of metabolites, fast liquid chromatography (LC) separation and electrospray ionization Fourier-transform ion cyclotron resonance mass spectrometry (ESI-FTICR MS) detection. An isotope reagent, (13)C-dansyl chloride, can be

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