1-(4-Methanesulfonyl-2-nitrophenyl)piperazine hydrochloride CAS 1172263-55-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1172263-55-6
Molecular FormulaC11H15N3O4S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(4-Methanesulfonyl-2-nitrophenyl)piperazine hydrochloride CAS 1172263-55-6 chemical structure

Description

CATO supplies 1-(4-Methanesulfonyl-2-nitrophenyl)piperazine hydrochloride (CAS 1172263-55-6), a certified reference material (molecular formula C11H15N3O4SHCl, MW 321.78 g/mol) for analytical method development and quality control.

Structurally, 1-(4-Methanesulfonyl-2-nitrophenyl)piperazine hydrochloride (C11H15N3O4SHCl) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 5.0, corresponding to approximately 5 ring(s) or double-bond equivalent(s). With a molecular weight of 321.78 g/mol, it falls into the moderately-high-molecular-weight range. 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 1-(4-Methanesulfonyl-2-nitrophenyl)piperazine 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 FormulaC11H15N3O4S HCl
Molecular Weight321.78 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms1

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