1H-pyrrolo[3,2-d]pyrimidin-4-ol CAS 39455-99-7

Purity 97%+In StockPharmaceutical Standards
CAS No.39455-99-7
Molecular FormulaC6H5N3O
Molecular Weight135.12 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1H-pyrrolo[3,2-d]pyrimidin-4-ol CAS 39455-99-7 chemical structure

Description

The occurrence of 1H-pyrrolo[3,2-d]pyrimidin-4-ol is closely related to an amide group, a hydroxyl group, an ether linkage, an aromatic ring system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 1H-pyrrolo[3,2-d]pyrimidin-4-ol (CAS 39455-99-7), a certified reference material (molecular formula C6H5N3O, MW 135.12 g/mol) for analytical method development and quality control.

Structurally, 1H-pyrrolo[3,2-d]pyrimidin-4-ol (C6H5N3O) contains an amide group, a hydroxyl group, an ether linkage, an aromatic ring system. The molecule exhibits a degree of unsaturation (DBE) of 6.0, corresponding to approximately 6 ring(s) or double-bond equivalent(s). With a molecular weight of 135.12 g/mol, it falls into the low-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 1H-pyrrolo[3,2-d]pyrimidin-4-ol 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 FormulaC6H5N3O
Molecular Weight135.12 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1968
Nitrogen Atoms3

Related H Standards

Recommended Standards

Why CATO?