1,1,1-Tris(4-hydroxyphenyl)ethane CAS 27955-94-8

Purity 97%+In StockPharmaceutical Standards
CAS No.27955-94-8
Molecular FormulaC20H18O3
Molecular Weight306.36 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1,1,1-Tris(4-hydroxyphenyl)ethane CAS 27955-94-8 chemical structure

Description

The occurrence of 1,1,1-Tris(4-hydroxyphenyl)ethane is closely related to a steroid core, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 1,1,1-Tris(4-hydroxyphenyl)ethane (CAS 27955-94-8), a certified reference material (molecular formula C20H18O3, MW 306.36 g/mol) for analytical method development and quality control.

Structurally, 1,1,1-Tris(4-hydroxyphenyl)ethane (C20H18O3) contains a steroid core, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 12.0, corresponding to approximately 12 ring(s) or double-bond equivalent(s). With a molecular weight of 306.36 g/mol, it falls into the moderately-high-molecular-weight range. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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

As a certified reference material (CRM), 1,1,1-Tris(4-hydroxyphenyl)ethane meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC20H18O3
Molecular Weight306.36 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1964

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