1-Methyl-3,5-dimethylenecyclohex-1-ene CAS 102236-48-6

Purity 97%+In StockPharmaceutical Standards
CAS No.102236-48-6
Molecular FormulaC9H12
Molecular Weight120.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-Methyl-3,5-dimethylenecyclohex-1-ene CAS 102236-48-6 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 1-Methyl-3,5-dimethylenecyclohex-1-ene.

1-Methyl-3,5-dimethylenecyclohex-1-ene (CAS 102236-48-6), molecular formula C9H12 and molecular weight 120.19 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 1-Methyl-3,5-dimethylenecyclohex-1-ene (C9H12) is characterized by an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by its non-polar molecular character, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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.

CATO manufactures 1-Methyl-3,5-dimethylenecyclohex-1-ene 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 FormulaC9H12
Molecular Weight120.19 g/mol
Purity97%+
StorageStore at 2-8°C
Solubility (reference)Soluble in methanol, acetonitrile, DMSO
StabilityStable under recommended storage conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986

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