2-(4-Iodobutyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane CAS 1236275-93-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1236275-93-6
Molecular FormulaC10H20BIO2
Molecular Weight309.98 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(4-Iodobutyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane CAS 1236275-93-6 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 2-(4-Iodobutyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane.

2-(4-Iodobutyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS 1236275-93-6) is a high-purity analytical reference standard with the molecular formula C10H20BIO2 and a molecular weight of 309.98 g/mol.

The molecular framework of 2-(4-Iodobutyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (C10H20BIO2) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution. 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC10H20BIO2
Molecular Weight309.98 g/mol
Purity97%+
StorageStore at room temperature
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityContains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)0.5
CAS Registry Year (est.)1990
Halogen ContentI-containing

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