Pyridine, 5-ethenyl-2-methyl-, polymer with diethenylbenzene and ethenylethylbenzene CAS 63690-51-7

Purity 97%+In StockPharmaceutical Standards
CAS No.63690-51-7
Molecular FormulaC10H12
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Pyridine, 5-ethenyl-2-methyl-, polymer with diethenylbenzene and ethenylethylbenzene CAS 63690-51-7 chemical structure

Description

Structurally, Pyridine, 5-ethenyl-2-methyl-, polymer with diethenylbenzene and ethenylethylbenzene (C10H12C10H10C8H9N) contains a nitrogen-containing heterocyclic scaffold, a nitrile group. The molecule exhibits a degree of unsaturation (DBE) of 14.0, corresponding to approximately 14 ring(s) or double-bond equivalent(s). With a molecular weight of 381.56 g/mol, it falls into the moderately-high-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

Pyridine, 5-ethenyl-2-methyl-, polymer with diethenylbenzene and ethenylethylbenzene (CAS 63690-51-7), molecular formula C10H12C10H10C8H9N and molecular weight 381.56 g/mol, is a CATO reference standard with documented purity and traceability.

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 Pyridine, 5-ethenyl-2-methyl-, polymer with diethenylbenzene and ethenylethylbenzene 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 FormulaC10H12 C10H10 C8H9N
Molecular Weight381.56 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1975
Nitrogen Atoms1

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