1-azido-5-iodonaphthalene CAS 63785-44-4

Purity 97%+In StockPharmaceutical Standards
CAS No.63785-44-4
Molecular FormulaC10H16IN3
Molecular Weight305.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-azido-5-iodonaphthalene CAS 63785-44-4 chemical structure

Description

The occurrence of 1-azido-5-iodonaphthalene is closely related to a nitrogen-containing heterocyclic scaffold, a nitrile group, iodine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

1-azido-5-iodonaphthalene (CAS 63785-44-4), molecular formula C10H16IN3 and molecular weight 305.16 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 1-azido-5-iodonaphthalene (C10H16IN3) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group, iodine 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).

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-azido-5-iodonaphthalene 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 FormulaC10H16IN3
Molecular Weight305.16 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1975
Halogen ContentI-containing
Nitrogen Atoms3

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