4,7-Methano-1H-indene, 3a,4,7,7a-tetrahydro-, polymer with 5-methylbicyclo[2.2.1]hept-2-ene CAS 69376-38-1

Purity 97%+In StockPharmaceutical Standards
CAS No.69376-38-1
Molecular FormulaC10H12
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4,7-Methano-1H-indene, 3a,4,7,7a-tetrahydro-, polymer with 5-methylbicyclo[2.2.1]hept-2-ene CAS 69376-38-1 chemical structure

Description

Structurally, 4,7-Methano-1H-indene, 3a,4,7,7a-tetrahydro-, polymer with 5-methylbicyclo[2.2.1]hept-2-ene (C10H12C8H12) contains a polycyclic aromatic system. The molecule exhibits a degree of unsaturation (DBE) of 7.0, corresponding to approximately 7 ring(s) or double-bond equivalent(s). With a molecular weight of 240.39 g/mol, it falls into the medium-molecular-weight range. 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).

CATO supplies 4,7-Methano-1H-indene, 3a,4,7,7a-tetrahydro-, polymer with 5-methylbicyclo[2.2.1]hept-2-ene (CAS 69376-38-1), a certified reference material (molecular formula C10H12C8H12, MW 240.39 g/mol) for analytical method development and quality control.

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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC10H12 C8H12
Molecular Weight240.39 g/mol
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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1976

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