3,4-Dimethoxyphenylzinc iodide 0.5 M in Tetrahydrofuran CAS 738580-38-6

Purity 97%+In StockPharmaceutical Standards
CAS No.738580-38-6
Molecular FormulaC8H9IO2Zn
Molecular Weight329.47 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,4-Dimethoxyphenylzinc iodide 0.5 M in Tetrahydrofuran CAS 738580-38-6 chemical structure

Description

CATO supplies 3,4-Dimethoxyphenylzinc iodide 0.5 M in Tetrahydrofuran (CAS 738580-38-6), a certified reference material (molecular formula C8H9IO2Zn, MW 329.47 g/mol) for analytical method development and quality control.

The molecular framework of 3,4-Dimethoxyphenylzinc iodide 0.5 M in Tetrahydrofuran (C8H9IO2Zn) is characterized by a salt form, a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by the polarity and ionization state of its functional groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures 3,4-Dimethoxyphenylzinc iodide 0.5 M in Tetrahydrofuran under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC8H9IO2Zn
Molecular Weight329.47 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at room temperature
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentI-containing

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