Phenylmagnesium Iodide (ca. 42% in Ethyl Ether, ca. 2mol/L) CAS 16002-63-4

Purity 97%+In StockPharmaceutical Standards
CAS No.16002-63-4
Molecular FormulaI
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Phenylmagnesium Iodide (ca. 42% in Ethyl Ether, ca. 2mol/L) CAS 16002-63-4 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 228.31 g/mol gives Phenylmagnesium Iodide (ca. 42% in Ethyl Ether, ca. 2mol/L) distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

Phenylmagnesium Iodide (ca. 42% in Ethyl Ether, ca. 2mol/L) (CAS 16002-63-4) is a high-purity analytical reference standard with the molecular formula IC6H5Mg and a molecular weight of 228.31 g/mol.

Based on its molecular formula IC6H5Mg, Phenylmagnesium Iodide (ca. 42% in Ethyl Ether, ca. 2mol/L) contains a salt form, iodine substitution, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 228.31 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 FormulaI C6H5 Mg
Molecular Weight228.31 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 methanol, acetonitrile, 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.)1961
Halogen ContentI-containing

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