(R)-1-(3-fluoro-5-methylphenyl)pentan-1-amine CAS 1213655-60-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1213655-60-7
Molecular FormulaC12H18FN
Molecular Weight195.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(R)-1-(3-fluoro-5-methylphenyl)pentan-1-amine CAS 1213655-60-7 chemical structure

Description

The occurrence of (R)-1-(3-fluoro-5-methylphenyl)pentan-1-amine is closely related to a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

(R)-1-(3-fluoro-5-methylphenyl)pentan-1-amine (CAS 1213655-60-7) is a high-purity analytical reference standard with the molecular formula C12H18FN and a molecular weight of 195.28 g/mol.

Based on its molecular formula C12H18FN, (R)-1-(3-fluoro-5-methylphenyl)pentan-1-amine contains a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 195.28 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.

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

CATO manufactures (R)-1-(3-fluoro-5-methylphenyl)pentan-1-amine 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 FormulaC12H18FN
Molecular Weight195.28 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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF-containing
Nitrogen Atoms1

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