1-Cyclopropoxy-3-ethyl-2-iodobenzene CAS 1243400-46-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1243400-46-5
Molecular FormulaC11H13IO
Molecular Weight288.12 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-Cyclopropoxy-3-ethyl-2-iodobenzene CAS 1243400-46-5 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 1-Cyclopropoxy-3-ethyl-2-iodobenzene.

CATO supplies 1-Cyclopropoxy-3-ethyl-2-iodobenzene (CAS 1243400-46-5), a certified reference material (molecular formula C11H13IO, MW 288.12 g/mol) for analytical method development and quality control.

1-Cyclopropoxy-3-ethyl-2-iodobenzene (C11H13IO) contains a hydroxyl group, an ether linkage, iodine substitution, an aromatic ring system. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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.

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 FormulaC11H13IO
Molecular Weight288.12 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at room temperature, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentI-containing

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