4-(o-Tolyl)-1,2,3,6-tetrahydropyridine Hydrochloride CAS 83674-77-5

Purity 97%+In StockPharmaceutical Standards
CAS No.83674-77-5
Molecular FormulaC12H15N
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(o-Tolyl)-1,2,3,6-tetrahydropyridine Hydrochloride CAS 83674-77-5 chemical structure

Description

The occurrence of 4-(o-Tolyl)-1,2,3,6-tetrahydropyridine Hydrochloride is closely related to a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

4-(o-Tolyl)-1,2,3,6-tetrahydropyridine Hydrochloride (CAS 83674-77-5), molecular formula C12H15NHCl and molecular weight 209.72 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution, 4-(o-Tolyl)-1,2,3,6-tetrahydropyridine Hydrochloride is typically off-white to pale yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 209.72 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.

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

As a certified reference material (CRM), 4-(o-Tolyl)-1,2,3,6-tetrahydropyridine Hydrochloride 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 FormulaC12H15N HCl
Molecular Weight209.72 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
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.)1980
Halogen ContentCl-containing
Nitrogen Atoms1

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