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Thermo Scientific Chemicals
3,4-Dimethoxybenzoic acid, 99+%
CAS: 93-07-2 | C9H10O4 | 182.175 g/mol
化学物質識別子
CAS93-07-2
IUPAC Name3,4-dimethoxybenzoic acid
Molecular FormulaC9H10O4
InChI KeyDAUAQNGYDSHRET-UHFFFAOYSA-N
SMILESCOC1=CC=C(C=C1OC)C(O)=O
さらに表示
仕様
スペックシート
スペックシートAppearance (Color)White
Assay (Aqueous acid-base Titration)≥99.0 to ≤101.0%
Melting Point (clear melt)179.0-186.0?C
FormPowder
Assay (Silylated GC)≥99.0%
3,4-Dimethoxybenzoic acid plays an important role in producing antibiotics and various dyes. They are used as intermediates for pharmaceuticals (especially for antipyretic analgesic, antirheumatism) and other organic synthesis. It is used as matrix for ionization of peptides, proteins and carbohydrates.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
3,4-Dimethoxybenzoic acid plays an important role in producing antibiotics and various dyes. They are used as intermediates for pharmaceuticals (especially for antipyretic analgesic, antirheumatism) and other organic synthesis. It is used as matrix for ionization of peptides, proteins and carbohydrates.
Solubility
Soluble in water (0.5 mg/ml at 15°C), chloroform, methanol, and 95% ethanol (50 mg/ml).
Notes
Incompatible with oxidizing agents. Store in a cool, dry condition in well sealed containers.
3,4-Dimethoxybenzoic acid plays an important role in producing antibiotics and various dyes. They are used as intermediates for pharmaceuticals (especially for antipyretic analgesic, antirheumatism) and other organic synthesis. It is used as matrix for ionization of peptides, proteins and carbohydrates.
Solubility
Soluble in water (0.5 mg/ml at 15°C), chloroform, methanol, and 95% ethanol (50 mg/ml).
Notes
Incompatible with oxidizing agents. Store in a cool, dry condition in well sealed containers.
RUO – Research Use Only
General References:
- Serdar Durdagi; Murat Şentürk; Deniz Ekinci; Halis Türker Balaydın; Süleyman Göksu; Ö. İrfan Küfrevioğlu; Alessio Innocenti; Andrea Scozzafava; Claudiu T. Supuran. Kinetic and docking studies of phenol-based inhibitors of carbonic anhydrase isoforms I, II, IX and XII evidence a new binding mode within the enzyme active site. Bioorganic & Medicinal Chemistry. 2011, 19 (4), 1381-1389.
- R G Dickinson; P V Baker; M E Franklin; W D Hooper. Facile hydrolysis of mebeverine in vitro and in vivo: negligible circulating concentrations of the drug after oral administration. Journal of Pharmaceutical Sciences. 1991, 80 (10), 952-957.