Sucralose EP Impurity I CAS 848642-13-7

Purity >95%In StockPharmacopoeial Impurity Standards
CAS No.848642-13-7
Molecular FormulaC6H11ClO5
Molecular Weight198.60 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Sucralose EP Impurity I CAS 848642-13-7 chemical structure

Description

CATO manufactures Sucralose EP Impurity I 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.

Sucralose EP Impurity I (CAS 848642-13-7) is a certified pharmaceutical impurity reference standard with the molecular formula C6H11ClO5 and a molecular weight of 198.60 g/mol.

Based on its molecular formula C6H11ClO5, Sucralose EP Impurity I contains a carbohydrate-derived structure, chlorine substitution; these features give the compound characteristic functional-group stretching vibrations in infrared spectroscopy. The molecular weight of 198.60 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

Recommended for quantitative analysis by HPLC, GC, LC-MS/MS, or GC-MS as an external calibration standard; it can also be used for spiked-recovery experiments, LOD/LOQ determination, and LC-MS/MS multiple-reaction-monitoring (MRM) calibration.

Physical & Chemical Properties

Molecular FormulaC6H11ClO5
Molecular Weight198.60 g/mol
Purity>95%
StorageStore at 2-8°C, keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, ethanol, DMSO, water
StabilityHygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)1.0
CAS Registry Year (est.)1987
Halogen ContentCl-containing

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