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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Sodium 4-aminosalicylate - ≥99% , CAS No.133-10-8
Synonyms
NCGC00159472-05 | Pasalon-rakeet | sodium 4-azanyl-2-oxidanyl-benzoate | SPECTRUM1500116 | Sodium 2-hydroxy-4-aminobenzoate | AKOS015963386 | HMS3652I08 | HMS3371F03 | FVVDKUPCWXUVNP-UHFFFAOYSA-M | HMS2230H22 | Salicylic acid, 4-amino-, sodium salt | EINE
Storage
Room temperature,Desiccated
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Why this grade ≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature,Desiccated 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.
Specifications Sinónimos
NCGC00159472-05 | Pasalon-rakeet | sodium 4-azanyl-2-oxidanyl-benzoate | SPECTRUM1500116 | Sodium 2-hydroxy-4-aminobenzoate | AKOS015963386 | HMS3652I08 | HMS3371F03 | FVVDKUPCWXUVNP-UHFFFAOYSA-M | HMS2230H22 | Salicylic acid, 4-amino-, sodium salt | EINE
Especificaciones y pureza
≥99%
Condiciones de almacenamiento de almacenamiento
Room temperature, Desiccated
Nombres e identificadores Pubchem Sid 488192270 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488192270 Sonrisas canónicas C1=CC(=C(C=C1N)O)C(=O)[O-].[Na+] IUPAC Name sodium;4-amino-2-hydroxybenzoate InChIKey FVVDKUPCWXUVNP-UHFFFAOYSA-M INCHI 1S/C7H7NO3.Na/c8-4-1-2-5(7(10)11)6(9)3-4;/h1-3,9H,8H2,(H,10,11);/q;+1/p-1 Isómeros SMILES C1=CC(=C(C=C1N)O)C(=O)[O-].[Na+] PubChem CID 2724368 Peso molecular 175.12
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 Clase 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 4-aminosalicylic acids Salicylic acids Aminobenzoic acids Benzoic acids m-Aminophenols Aniline and substituted anilines Benzoyl derivatives 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Vinylogous acids Amino acids Carboxylic acid salts Monocarboxylic acids and derivatives Carboxylic acids Hydrocarbon derivatives Organic oxides Organic sodium salts Organic zwitterions Organooxygen compounds Organopnictogen compounds Primary amines Molecular Framework Aromatic homomonocyclic compounds Substituents 4-aminosalicylic acid - Aminosalicylic acid - Salicylic acid - Aminobenzoic acid or derivatives - Aminobenzoic acid - Benzoic acid - M-aminophenol - Aminophenol - Aniline or substituted anilines - Benzoyl - Phenol - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Vinylogous acid - Carboxylic acid salt - Amino acid - Amino acid or derivatives - Carboxylic acid - Organic alkali metal salt - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Primary amine - Organic zwitterion - Organic salt - Organic sodium salt - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Amine - Aromatic homomonocyclic compound Descripción 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 organic molecular entity 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.
Estructura 3D Objetivos asociados (humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Punto de fusión (°C) 265-270℃ Peso molecular 175.120 g/mol XLogP3 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 1 Exact Mass 175.025 Da Monoisotopic Mass 175.025 Da Topological Polar Surface Area 86.400 Ų Heavy Atom Count 12 Formal Charge 0 Complexity 165.000 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 2
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