4-Chloro-2,3-dihydro-1H-pyrrolo[2,3-d]pyridazine CAS 1354455-05-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1354455-05-2
Molecular FormulaC6H6ClN3
Molecular Weight155.58 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Chloro-2,3-dihydro-1H-pyrrolo[2,3-d]pyridazine CAS 1354455-05-2 chemical structure

Description

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.

4-Chloro-2,3-dihydro-1H-pyrrolo[2,3-d]pyridazine (CAS 1354455-05-2), molecular formula C6H6ClN3 and molecular weight 155.58 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a nitrile group, chlorine substitution, an aromatic ring system, 4-Chloro-2,3-dihydro-1H-pyrrolo[2,3-d]pyridazine is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 155.58 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

As a certified reference material (CRM), 4-Chloro-2,3-dihydro-1H-pyrrolo[2,3-d]pyridazine 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 FormulaC6H6ClN3
Molecular Weight155.58 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor)
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.)1991
Halogen ContentCl-containing
Nitrogen Atoms3

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