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· · COA & SDS available for every product · Same-day shipping on in-stock items 3-Aminosalicylic Acid - ≥98%(HPLC) , CAS No.570-23-0
Synonyms
AC-23862 | SY049223 | 3-Amino-2-hydroxybenzoic acid (3-Aminosalicylic acid) | 3-aminosalicyclic acid | 3-amino-(8CI)salicylic acid | PD164136 | MESALAZINE IMPURITY F [EP IMPURITY] | 3-amino-2-hydroxybenzoate | 3-amino-2-hydroxy-benzoate | NSC 285111 | NSC
Storage
Argon charged,Room temperature
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Why this grade ≥98%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Argon charged,Room temperature Ships Normal Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview 3-Aminosalicylic acid acts as an oxygen, nitrogen donor ligand and forms complexes with silver.
Specifications Synonyms
AC-23862 | SY049223 | 3-Amino-2-hydroxybenzoic acid (3-Aminosalicylic acid) | 3-aminosalicyclic acid | 3-amino-(8CI)salicylic acid | PD164136 | MESALAZINE IMPURITY F [EP IMPURITY] | 3-amino-2-hydroxybenzoate | 3-amino-2-hydroxy-benzoate | NSC 285111 | NSC
Specifications & Purity
≥98%(HPLC)
Storage
Argon charged, Room temperature
Names and Identifiers Pubchem Sid 488184142 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488184142 Canonical Smiles C1=CC(=C(C(=C1)N)O)C(=O)O IUPAC Name 3-amino-2-hydroxybenzoic acid InChIKey IQGMRVWUTCYCST-UHFFFAOYSA-N INCHI 1S/C7H7NO3/c8-5-3-1-2-4(6(5)9)7(10)11/h1-3,9H,8H2,(H,10,11) Isomeric SMILES C1=CC(=C(C(=C1)N)O)C(=O)O WGK Germany 3 Molecular Weight 153.14 Beilstein 2090430 Reaxy-Rn 2090427 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2090427&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Benzenoids Class Benzene and substituted derivatives Subclass Benzoic acids and derivatives Intermediate Tree Nodes Hydroxybenzoic acid derivatives - Salicylic acid and derivatives - Aminosalicylic acids and derivatives Direct Parent Aminosalicylic acids Alternative Parents 3-aminosalicylic acids Salicylic acids Aminobenzoic acids Benzoic acids o-Aminophenols Aniline and substituted anilines Benzoyl derivatives 1-hydroxy-4-unsubstituted benzenoids Vinylogous acids Amino acids Monocarboxylic acids and derivatives Carboxylic acids Hydrocarbon derivatives Organic oxides Organooxygen compounds Organopnictogen compounds Primary amines Molecular Framework Aromatic homomonocyclic compounds Substituents 3-aminosalicylic acid - Aminosalicylic acid - Salicylic acid - Aminobenzoic acid or derivatives - Aminobenzoic acid - Benzoic acid - Aniline or substituted anilines - O-aminophenol - Aminophenol - Benzoyl - 1-hydroxy-4-unsubstituted benzenoid - Phenol - Vinylogous acid - Amino acid - Amino acid or derivatives - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Carboxylic acid - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Primary amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Amine - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as aminosalicylic acids. These are salicylic acids carrying an amino group on the benzene ring. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Soluble in potassium hydroxide. Slightly soluble in water. Sensitivity Air & light sensitive Melt Point(°C) 240 °C Molecular Weight 153.140 g/mol XLogP3 0.900 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 1 Exact Mass 153.043 Da Monoisotopic Mass 153.043 Da Topological Polar Surface Area 83.600 Ų Heavy Atom Count 11 Formal Charge 0 Complexity 160.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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