1-(Trans-2-Phenylethenyl)-4-(phenylethynyl)benzene CAS 173035-17-1

Purity 97%+In StockPharmaceutical Standards
CAS No.173035-17-1
Molecular FormulaC22H16
Molecular Weight280.36 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(Trans-2-Phenylethenyl)-4-(phenylethynyl)benzene CAS 173035-17-1 chemical structure

Description

The occurrence of 1-(Trans-2-Phenylethenyl)-4-(phenylethynyl)benzene is closely related to a polycyclic aromatic system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

1-(Trans-2-Phenylethenyl)-4-(phenylethynyl)benzene (CAS 173035-17-1), molecular formula C22H16 and molecular weight 280.36 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, 1-(Trans-2-Phenylethenyl)-4-(phenylethynyl)benzene (C22H16) contains a polycyclic aromatic system. The molecule exhibits a degree of unsaturation (DBE) of 15.0, corresponding to approximately 15 ring(s) or double-bond equivalent(s). With a molecular weight of 280.36 g/mol, it falls into the medium-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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-(Trans-2-Phenylethenyl)-4-(phenylethynyl)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 FormulaC22H16
Molecular Weight280.36 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2006

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