4,6-Dichloro-2-(dimethylamino)pyrimidine-5-carbaldehyde CAS 15138-41-7

Purity 97%+In StockPharmaceutical Standards
CAS No.15138-41-7
Molecular FormulaC7H7Cl2N3O
Molecular Weight220.06 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4,6-Dichloro-2-(dimethylamino)pyrimidine-5-carbaldehyde CAS 15138-41-7 chemical structure

Description

As a certified reference material (CRM), 4,6-Dichloro-2-(dimethylamino)pyrimidine-5-carbaldehyde 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.

4,6-Dichloro-2-(dimethylamino)pyrimidine-5-carbaldehyde (CAS 15138-41-7), molecular formula C7H7Cl2N3O and molecular weight 220.06 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 4,6-Dichloro-2-(dimethylamino)pyrimidine-5-carbaldehyde (C7H7Cl2N3O) is characterized by an amide group, a hydroxyl group, an ether linkage, chlorine substitution, 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

Physical & Chemical Properties

Molecular FormulaC7H7Cl2N3O
Molecular Weight220.06 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1961
Halogen ContentCl-containing
Nitrogen Atoms3

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