6-(tert-Butylsulfanyl)pyridine-3-carboximidamide hydrochloride CAS 1423025-27-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1423025-27-7
Molecular FormulaC10H15N3S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-(tert-Butylsulfanyl)pyridine-3-carboximidamide hydrochloride CAS 1423025-27-7 chemical structure

Description

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality, chlorine substitution, 6-(tert-Butylsulfanyl)pyridine-3-carboximidamide hydrochloride is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 245.77 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO supplies 6-(tert-Butylsulfanyl)pyridine-3-carboximidamide hydrochloride (CAS 1423025-27-7), a certified reference material (molecular formula C10H15N3SHCl, MW 245.77 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 6-(tert-Butylsulfanyl)pyridine-3-carboximidamide 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 FormulaC10H15N3S HCl
Molecular Weight245.77 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms1

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