(S)-1-(2-(Trifluoromethyl)pyrimidin-5-yl)ethanamine CAS 1948237-00-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1948237-00-0
Molecular FormulaC7H8F3N3
Molecular Weight191.15 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(S)-1-(2-(Trifluoromethyl)pyrimidin-5-yl)ethanamine CAS 1948237-00-0 chemical structure

Description

(S)-1-(2-(Trifluoromethyl)pyrimidin-5-yl)ethanamine (C7H8F3N3) contains a nitrile group, fluorine substitution, an aromatic ring system. Halogen substitution raises its density and boiling point; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

(S)-1-(2-(Trifluoromethyl)pyrimidin-5-yl)ethanamine (CAS 1948237-00-0), molecular formula C7H8F3N3 and molecular weight 191.15 g/mol, is a CATO reference standard with documented purity and traceability.

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 (S)-1-(2-(Trifluoromethyl)pyrimidin-5-yl)ethanamine 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 FormulaC7H8F3N3
Molecular Weight191.15 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 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.)1996
Halogen ContentF-containing
Nitrogen Atoms3

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