4-((3,3,4,4,5,5,6,6,6-Nonafluorohexyl)thio)phenol CAS 892155-14-5

Purity 97%+In StockPharmaceutical Standards
CAS No.892155-14-5
Molecular FormulaC12H9F9OS
Molecular Weight372.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-((3,3,4,4,5,5,6,6,6-Nonafluorohexyl)thio)phenol CAS 892155-14-5 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 4-((3,3,4,4,5,5,6,6,6-Nonafluorohexyl)thio)phenol.

4-((3,3,4,4,5,5,6,6,6-Nonafluorohexyl)thio)phenol (CAS 892155-14-5), molecular formula C12H9F9OS and molecular weight 372.25 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to sulfur-containing functionality, a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system, 4-((3,3,4,4,5,5,6,6,6-Nonafluorohexyl)thio)phenol is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 372.25 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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 4-((3,3,4,4,5,5,6,6,6-Nonafluorohexyl)thio)phenol 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 FormulaC12H9F9OS
Molecular Weight372.25 g/mol
Purity97%+
StorageStore at room temperature
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Sulfur Atoms1

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