4-Chloro-n-(3-morpholinopropyl)-3-nitrobenzenesulfonamide hydrochloride CAS 1049735-87-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1049735-87-6
Molecular FormulaC13H18ClN3O5S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Chloro-n-(3-morpholinopropyl)-3-nitrobenzenesulfonamide hydrochloride CAS 1049735-87-6 chemical structure

Description

Based on its molecular formula C13H18ClN3O5SHCl, 4-Chloro-n-(3-morpholinopropyl)-3-nitrobenzenesulfonamide hydrochloride contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 400.27 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies 4-Chloro-n-(3-morpholinopropyl)-3-nitrobenzenesulfonamide hydrochloride (CAS 1049735-87-6), a certified reference material (molecular formula C13H18ClN3O5SHCl, MW 400.27 g/mol) for analytical method development and quality control.

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 4-Chloro-n-(3-morpholinopropyl)-3-nitrobenzenesulfonamide hydrochloride 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 FormulaC13H18ClN3O5S HCl
Molecular Weight400.27 g/mol
Purity97%+
StorageStore in a cool place (≤25°C), protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms1

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