1-Fluoro-2-methyl-4-(2-methylallyl)benzene CAS 869493-79-8

Purity 97%+In StockPharmaceutical Standards
CAS No.869493-79-8
Molecular FormulaC11H13F
Molecular Weight164.22 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-Fluoro-2-methyl-4-(2-methylallyl)benzene CAS 869493-79-8 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 164.22 g/mol gives 1-Fluoro-2-methyl-4-(2-methylallyl)benzene distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

1-Fluoro-2-methyl-4-(2-methylallyl)benzene (CAS 869493-79-8), molecular formula C11H13F and molecular weight 164.22 g/mol, is a CATO reference standard with documented purity and traceability.

1-Fluoro-2-methyl-4-(2-methylallyl)benzene (C11H13F) contains fluorine substitution, an aromatic ring system. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; 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.

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-Fluoro-2-methyl-4-(2-methylallyl)benzene 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 FormulaC11H13F
Molecular Weight164.22 g/mol
Purity97%+
StorageStore at 2-8°C, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing

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Why CATO?