3,4,5,6,7,8-Hexafluoro-1-methoxyisoquinoline CAS 13180-44-4

Purity 97%+In StockPharmaceutical Standards
CAS No.13180-44-4
Molecular FormulaC10H3F6NO
Molecular Weight267.13 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,4,5,6,7,8-Hexafluoro-1-methoxyisoquinoline CAS 13180-44-4 chemical structure

Description

Structurally, 3,4,5,6,7,8-Hexafluoro-1-methoxyisoquinoline (C10H3F6NO) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. 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 267.13 g/mol, it falls into the medium-molecular-weight range. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies 3,4,5,6,7,8-Hexafluoro-1-methoxyisoquinoline (CAS 13180-44-4), a certified reference material (molecular formula C10H3F6NO, MW 267.13 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.

CATO manufactures 3,4,5,6,7,8-Hexafluoro-1-methoxyisoquinoline 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 FormulaC10H3F6NO
Molecular Weight267.13 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1960
Halogen ContentF-containing
Nitrogen Atoms1

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