n-Butyl-3-iodoaniline hydrochloride CAS 1311316-48-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1311316-48-9
Molecular FormulaC10H14IN
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

n-Butyl-3-iodoaniline hydrochloride CAS 1311316-48-9 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including n-Butyl-3-iodoaniline hydrochloride.

n-Butyl-3-iodoaniline hydrochloride (CAS 1311316-48-9), molecular formula C10H14INHCl and molecular weight 311.59 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, n-Butyl-3-iodoaniline hydrochloride (C10H14INHCl) contains a nitrile group, chlorine/iodine substitution. The molecule exhibits a degree of unsaturation (DBE) of 3.0, corresponding to approximately 3 ring(s) or double-bond equivalent(s). With a molecular weight of 311.59 g/mol, it falls into the moderately-high-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 n-Butyl-3-iodoaniline hydrochloride 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 FormulaC10H14IN HCl
Molecular Weight311.59 g/mol
AppearanceWhite to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light
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)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1990
Halogen ContentCl/I-containing
Nitrogen Atoms1

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