1-Undecanol,11,11'-[1,2-phenylenebis(oxy)]bis- (9CI) 123934-38-3 ACMC-20dsca CAS 123934-38-3

Purity 97%+In StockPharmaceutical Standards
CAS No.123934-38-3
Molecular FormulaC28H50O4
Molecular Weight450.69 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-Undecanol,11,11'-[1,2-phenylenebis(oxy)]bis- (9CI)
123934-38-3
ACMC-20dsca CAS 123934-38-3 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 450.69 g/mol gives 1-Undecanol,11,11'-[1,2-phenylenebis(oxy)]bis- (9CI) 123934-38-3 ACMC-20dsca distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

1-Undecanol,11,11'-[1,2-phenylenebis(oxy)]bis- (9CI) 123934-38-3 ACMC-20dsca (CAS 123934-38-3), molecular formula C28H50O4 and molecular weight 450.69 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a steroid core, a hydroxyl group, an ether linkage, 1-Undecanol,11,11'-[1,2-phenylenebis(oxy)]bis- (9CI) 123934-38-3 ACMC-20dsca is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 450.69 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC28H50O4
Molecular Weight450.69 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at room temperature, keep sealed and dry
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.)1992

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Why CATO?