6-Fluoro-1,2,3,4-tetrahydro-naphthalen-2-ylamine hydrochloride CAS 852660-54-9

Purity 97%+In StockPharmaceutical Standards
CAS No.852660-54-9
Molecular FormulaC10H12FN
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-Fluoro-1,2,3,4-tetrahydro-naphthalen-2-ylamine hydrochloride CAS 852660-54-9 chemical structure

Description

Based on its molecular formula C10H12FNHCl, 6-Fluoro-1,2,3,4-tetrahydro-naphthalen-2-ylamine hydrochloride contains a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine/chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 201.67 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO supplies 6-Fluoro-1,2,3,4-tetrahydro-naphthalen-2-ylamine hydrochloride (CAS 852660-54-9), a certified reference material (molecular formula C10H12FNHCl, MW 201.67 g/mol) for analytical method development and quality control.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC10H12FN HCl
Molecular Weight201.67 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
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.)1987
Halogen ContentF/Cl-containing
Nitrogen Atoms1

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