11-Chloro-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline CAS 5778-71-2

Purity 97%+In StockPharmaceutical Standards
CAS No.5778-71-2
Molecular FormulaC14H14ClN
Molecular Weight231.72 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

11-Chloro-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline CAS 5778-71-2 chemical structure

Description

The occurrence of 11-Chloro-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline 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.

11-Chloro-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline (CAS 5778-71-2), molecular formula C14H14ClN and molecular weight 231.72 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 11-Chloro-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline (C14H14ClN) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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), 11-Chloro-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline 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 FormulaC14H14ClN
Molecular Weight231.72 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958
Halogen ContentCl-containing
Nitrogen Atoms1

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