1-(3,5-Diacetoxyphenyl)-1-bromoethane 1026420-83-6 5-(1-Bromoethyl)-1,3-benzenediol 1,3-Diacetate CAS 1026420-83-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1026420-83-6
Molecular FormulaC12H13BrO4
Molecular Weight301.13 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(3,5-Diacetoxyphenyl)-1-bromoethane
1026420-83-6
5-(1-Bromoethyl)-1,3-benzenediol 1,3-Diacetate CAS 1026420-83-6 chemical structure

Description

As a certified reference material (CRM), 1-(3,5-Diacetoxyphenyl)-1-bromoethane 1026420-83-6 5-(1-Bromoethyl)-1,3-benzenediol 1,3-Diacetate meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

CATO supplies 1-(3,5-Diacetoxyphenyl)-1-bromoethane 1026420-83-6 5-(1-Bromoethyl)-1,3-benzenediol 1,3-Diacetate (CAS 1026420-83-6), a certified reference material (molecular formula C12H13BrO4, MW 301.13 g/mol) for analytical method development and quality control.

The molecular framework of 1-(3,5-Diacetoxyphenyl)-1-bromoethane 1026420-83-6 5-(1-Bromoethyl)-1,3-benzenediol 1,3-Diacetate (C12H13BrO4) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, bromine substitution, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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

Physical & Chemical Properties

Molecular FormulaC12H13BrO4
Molecular Weight301.13 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentBr-containing

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