2-Butyl-6-methyl-6H-pyrrolo[3,4-d]pyrimidin-4-amine CAS 1707563-26-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1707563-26-5
Molecular FormulaC11H16N4
Molecular Weight204.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Butyl-6-methyl-6H-pyrrolo[3,4-d]pyrimidin-4-amine CAS 1707563-26-5 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 2-Butyl-6-methyl-6H-pyrrolo[3,4-d]pyrimidin-4-amine.

2-Butyl-6-methyl-6H-pyrrolo[3,4-d]pyrimidin-4-amine (CAS 1707563-26-5), molecular formula C11H16N4 and molecular weight 204.27 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, 2-Butyl-6-methyl-6H-pyrrolo[3,4-d]pyrimidin-4-amine is typically off-white to pale yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 204.27 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).

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

As a certified reference material (CRM), 2-Butyl-6-methyl-6H-pyrrolo[3,4-d]pyrimidin-4-amine meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC11H16N4
Molecular Weight204.27 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.)1994
Nitrogen Atoms4

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