n-(Prop-2-yn-1-yl)-1,3-thiazol-2-amine CAS 1250676-92-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1250676-92-6
Molecular FormulaC6H6N2S
Molecular Weight138.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

n-(Prop-2-yn-1-yl)-1,3-thiazol-2-amine CAS 1250676-92-6 chemical structure

Description

CATO supplies n-(Prop-2-yn-1-yl)-1,3-thiazol-2-amine (CAS 1250676-92-6), a certified reference material (molecular formula C6H6N2S, MW 138.19 g/mol) for analytical method development and quality control.

The molecular framework of n-(Prop-2-yn-1-yl)-1,3-thiazol-2-amine (C6H6N2S) is characterized by a nitrile group, sulfur-containing functionality, an aromatic ring system. 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. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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-(Prop-2-yn-1-yl)-1,3-thiazol-2-amine 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 FormulaC6H6N2S
Molecular Weight138.19 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Nitrogen Atoms2
Sulfur Atoms1

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