(S)-3-Iodo-2,2'-bis(methoxymethoxy)-1,1'-binaphthalene CAS 497826-57-0

Purity 97%+In StockPharmaceutical Standards
CAS No.497826-57-0
Molecular FormulaC24H21IO4
Molecular Weight500.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(S)-3-Iodo-2,2'-bis(methoxymethoxy)-1,1'-binaphthalene CAS 497826-57-0 chemical structure

Description

CATO supplies (S)-3-Iodo-2,2'-bis(methoxymethoxy)-1,1'-binaphthalene (CAS 497826-57-0), a certified reference material (molecular formula C24H21IO4, MW 500.33 g/mol) for analytical method development and quality control.

Owing to a flavonoid core, a hydroxyl group, an ether linkage, iodine substitution, (S)-3-Iodo-2,2'-bis(methoxymethoxy)-1,1'-binaphthalene is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 500.33 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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.

CATO manufactures (S)-3-Iodo-2,2'-bis(methoxymethoxy)-1,1'-binaphthalene under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC24H21IO4
Molecular Weight500.33 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at room temperature, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentI-containing

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