N-(5-Methyl-1,3,4-thiadiazol-2-yl)acetimidamide CAS 56684-77-6

Purity 97%+In StockPharmaceutical Standards
CAS No.56684-77-6
Molecular FormulaC5H8N4S
Molecular Weight156.21 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(5-Methyl-1,3,4-thiadiazol-2-yl)acetimidamide CAS 56684-77-6 chemical structure

Description

The molecular framework of N-(5-Methyl-1,3,4-thiadiazol-2-yl)acetimidamide (C5H8N4S) is characterized by a nitrile group, sulfur-containing functionality. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

N-(5-Methyl-1,3,4-thiadiazol-2-yl)acetimidamide (CAS 56684-77-6) is a high-purity analytical reference standard with the molecular formula C5H8N4S and a molecular weight of 156.21 g/mol.

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 N-(5-Methyl-1,3,4-thiadiazol-2-yl)acetimidamide 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 FormulaC5H8N4S
Molecular Weight156.21 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1973
Nitrogen Atoms4
Sulfur Atoms1

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