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· · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock Methyl 3,4-methoxy-5-hydroxybenzoate - Moligand™ , CAS No.83011-43-2
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. Synonyms
AMY33323 | DTXSID80370056 | 3,4-dimethoxy-5-hydroxybenzoic acid methyl ester, AldrichCPR | Methyl 3,4-dimethoxy-5-hydroxybenzoate | methyl 3,4-dimethoxy-5-hydroxy-benzoate | HY-N3287 | AS-76337 | 3,4-Dimethoxy-5-hydroxybenzoic acid methyl ester | methyl 3
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Why this grade Moligand™ Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C Ships Wet ice 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 Synonymes
AMY33323 | DTXSID80370056 | 3,4-dimethoxy-5-hydroxybenzoic acid methyl ester, AldrichCPR | Methyl 3,4-dimethoxy-5-hydroxybenzoate | methyl 3,4-dimethoxy-5-hydroxy-benzoate | HY-N3287 | AS-76337 | 3,4-Dimethoxy-5-hydroxybenzoic acid methyl ester | methyl 3
Spécifications et pureté
Moligand™
Conditions de stockage de stockage
Store at 2-8°C
Expédié en
Wet ice
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Noms et identifiants Sourires canoniques
COC1=CC(=CC(=C1OC)O)C(=O)OC
IUPAC Name
methyl 3-hydroxy-4,5-dimethoxybenzoate
InChIKey
LCIFXEQPXQVBGL-UHFFFAOYSA-N
INCHI
1S/C10H12O5/c1-13-8-5-6(10(12)15-3)4-7(11)9(8)14-2/h4-5,11H,1-3H3
Isomères SMILES
COC1=CC(=CC(=C1OC)O)C(=O)OC
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2811280&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 Classe Benzene and substituted derivatives Subclass Benzoic acids and derivatives Intermediate Tree Nodes Hydroxybenzoic acid derivatives Direct Parent Gallic acid and derivatives Alternative Parents m-Hydroxybenzoic acid esters P-methoxybenzoic acids and derivatives M-methoxybenzoic acids and derivatives Methoxyphenols Dimethoxybenzenes Phenoxy compounds Benzoyl derivatives Anisoles Alkyl aryl ethers 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Methyl esters Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic homomonocyclic compounds Substituents Gallic acid or derivatives - M-hydroxybenzoic acid ester - M-methoxybenzoic acid or derivatives - P-methoxybenzoic acid or derivatives - Benzoate ester - Methoxyphenol - Dimethoxybenzene - O-dimethoxybenzene - Anisole - Phenoxy compound - Benzoyl - Phenol ether - Methoxybenzene - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Alkyl aryl ether - Phenol - Methyl ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Ether - Carboxylic acid derivative - Organic oxide - Organooxygen compound - Organic oxygen compound - Hydrocarbon derivative - Aromatic homomonocyclic compound Description 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.
Structure 3D Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Sensibilité Hygroscopic Indice de réfraction n20D1.53 (Predicted) Point d'ébullition (°C) ~366.6° C at 760 mmHg (Predicted) Point de fusion (°C) 97.75° C (Predicted) Poids moléculaire 212.200 g/mol XLogP3 1.400 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 4 Exact Mass 212.068 Da Monoisotopic Mass 212.068 Da Topological Polar Surface Area 65.000 Ų Heavy Atom Count 15 Formal Charge 0 Complexity 218.000 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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View Moligand™ grade guide →
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