7-Methyl-1,2,3,4-tetrahydrocyclopenta[b]indole CAS 1130-93-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1130-93-4
Molecular FormulaC12H13N
Molecular Weight171.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

7-Methyl-1,2,3,4-tetrahydrocyclopenta[b]indole CAS 1130-93-4 chemical structure

Description

The occurrence of 7-Methyl-1,2,3,4-tetrahydrocyclopenta[b]indole is closely related to a nitrogen-containing heterocyclic scaffold, a nitrile group in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 7-Methyl-1,2,3,4-tetrahydrocyclopenta[b]indole (CAS 1130-93-4), a certified reference material (molecular formula C12H13N, MW 171.24 g/mol) for analytical method development and quality control.

7-Methyl-1,2,3,4-tetrahydrocyclopenta[b]indole (C12H13N) contains a nitrogen-containing heterocyclic scaffold, a nitrile group. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 7-Methyl-1,2,3,4-tetrahydrocyclopenta[b]indole 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 FormulaC12H13N
Molecular Weight171.24 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.)1957
Nitrogen Atoms1

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