N-(3-(1H-imidazol-1-yl)propyl)-5-phenyl-1H-[1,2,3]triazolo[4,5-d]pyrimidin-7-amine CAS 565236-29-5

Purity 97%+In StockPharmaceutical Standards
CAS No.565236-29-5
Molecular FormulaC16H16N8
Molecular Weight320.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(3-(1H-imidazol-1-yl)propyl)-5-phenyl-1H-[1,2,3]triazolo[4,5-d]pyrimidin-7-amine CAS 565236-29-5 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including N-(3-(1H-imidazol-1-yl)propyl)-5-phenyl-1H-[1,2,3]triazolo[4,5-d]pyrimidin-7-amine.

N-(3-(1H-imidazol-1-yl)propyl)-5-phenyl-1H-[1,2,3]triazolo[4,5-d]pyrimidin-7-amine (CAS 565236-29-5) is a high-purity analytical reference standard with the molecular formula C16H16N8 and a molecular weight of 320.35 g/mol.

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, N-(3-(1H-imidazol-1-yl)propyl)-5-phenyl-1H-[1,2,3]triazolo[4,5-d]pyrimidin-7-amine is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 320.35 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC16H16N8
Molecular Weight320.35 g/mol
AppearancePale yellow to yellow crystalline powder
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)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1984
Nitrogen Atoms8

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