(R)-3-Methylisobenzofuran-1(3H)-one CAS 3413-14-7

Purity 97%+In StockPharmaceutical Standards
CAS No.3413-14-7
Molecular FormulaC9H8O2
Molecular Weight148.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(R)-3-Methylisobenzofuran-1(3H)-one CAS 3413-14-7 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 (R)-3-Methylisobenzofuran-1(3H)-one.

(R)-3-Methylisobenzofuran-1(3H)-one (CAS 3413-14-7) is a high-purity analytical reference standard with the molecular formula C9H8O2 and a molecular weight of 148.16 g/mol.

Owing to a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system, (R)-3-Methylisobenzofuran-1(3H)-one is typically off-white to pale yellow liquid. Its solid-state physicochemical attributes — including a molecular weight of 148.16 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

As a certified reference material (CRM), (R)-3-Methylisobenzofuran-1(3H)-one 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 FormulaC9H8O2
Molecular Weight148.16 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1957

Related R Standards

Recommended Standards

Why CATO?