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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Methyl 3,4,5-trimethoxyanthranilate - ≥99% , CAS No.5035-82-5
Synonyms
A871586 | SMR000062595 | InChI=1/C11H15NO5/c1-14-7-5-6(11(13)17-4)8(12)10(16-3)9(7)15-2/h5H,12H2,1-4H | STK865517 | NSC80816 | NSC-80816 | SR-01000510943 | FT-0628432 | Benzoic acid, 2-amino-3,4,5-trimethoxy-, methyl ester | EINECS 225-728-8 | SCHEMBL4734
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
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Why this grade ≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C,Argon charged Ships Ice chest + Ice pads 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
A871586 | SMR000062595 | InChI=1/C11H15NO5/c1-14-7-5-6(11(13)17-4)8(12)10(16-3)9(7)15-2/h5H, 12H2, 1-4H | STK865517 | NSC80816 | NSC-80816 | SR-01000510943 | FT-0628432 | Benzoic acid, 2-amino-3, 4, 5-trimethoxy-, methyl ester | EINECS 225-728-8 | SCHEMBL4734
Especificaciones y pureza
≥99%
Condiciones de almacenamiento de almacenamiento
Store at -20°C, Argon charged
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores Sonrisas canónicas COC1=C(C(=C(C(=C1)C(=O)OC)N)OC)OC IUPAC Name methyl 2-amino-3,4,5-trimethoxybenzoate InChIKey UPVUQELOASQBMY-UHFFFAOYSA-N INCHI 1S/C11H15NO5/c1-14-7-5-6(11(13)17-4)8(12)10(16-3)9(7)15-2/h5H,12H2,1-4H3 Isómeros SMILES COC1=C(C(=C(C(=C1)C(=O)OC)N)OC)OC WGK Alemania 3 Peso molecular 241.24 Reaxy-Rn 2142334 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2142334&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 Clase Benzene and substituted derivatives Subclass Benzoic acids and derivatives Intermediate Tree Nodes Hydroxybenzoic acid derivatives Direct Parent Gallic acid and derivatives Alternative Parents P-methoxybenzoic acids and derivatives M-methoxybenzoic acids and derivatives Aminobenzoic acids and derivatives Benzoic acid esters Aminophenyl ethers Methoxyanilines Anisoles Phenoxy compounds Benzoyl derivatives Methoxybenzenes Alkyl aryl ethers Vinylogous amides Methyl esters Amino acids and derivatives Monocarboxylic acids and derivatives Organopnictogen compounds Hydrocarbon derivatives Organic oxides Primary amines Molecular Framework Aromatic homomonocyclic compounds Substituents Gallic acid or derivatives - M-methoxybenzoic acid or derivatives - P-methoxybenzoic acid or derivatives - Aminobenzoic acid or derivatives - Benzoate ester - Aminophenyl ether - Methoxyaniline - Anisole - Phenoxy compound - Benzoyl - Phenol ether - Aniline or substituted anilines - Methoxybenzene - Alkyl aryl ether - Vinylogous amide - Methyl ester - Amino acid or derivatives - Carboxylic acid ester - Ether - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Amine - Primary amine - Organooxygen compound - Organic oxide - Organic nitrogen compound - Organonitrogen compound - Aromatic homomonocyclic compound Descripción This compound belongs to the class of organic compounds known as gallic acid and derivatives. These are compounds containing a 3,4,5-trihydroxybenzoic acid moiety. 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.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Punto de inflamación (°F) 235.4 °F Punto de inflamación (°C) 113 °C Punto de ebullición (°C) 127-140 °C/0.1 mmHg (lit.) Punto de fusión (°C) 44-45 °C (lit.) Peso molecular 241.240 g/mol XLogP3 1.600 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 5 Exact Mass 241.095 Da Monoisotopic Mass 241.095 Da Topological Polar Surface Area 80.000 Ų Heavy Atom Count 17 Formal Charge 0 Complexity 260.000 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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