(3-Methyl-4-(pentyloxy)phenyl)methanol CAS 1443339-47-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1443339-47-6
Molecular FormulaC13H20O2
Molecular Weight208.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(3-Methyl-4-(pentyloxy)phenyl)methanol CAS 1443339-47-6 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 (3-Methyl-4-(pentyloxy)phenyl)methanol.

(3-Methyl-4-(pentyloxy)phenyl)methanol (CAS 1443339-47-6) is a high-purity analytical reference standard with the molecular formula C13H20O2 and a molecular weight of 208.30 g/mol.

Structurally, (3-Methyl-4-(pentyloxy)phenyl)methanol (C13H20O2) contains a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. The molecule exhibits a degree of unsaturation (DBE) of 4.0, corresponding to approximately 4 ring(s) or double-bond equivalent(s). With a molecular weight of 208.30 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.

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), (3-Methyl-4-(pentyloxy)phenyl)methanol 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 FormulaC13H20O2
Molecular Weight208.30 g/mol
AppearanceOff-white to pale yellow crystalline powder
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.)1992

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