1-(2-Fluorobenzyl)-1-methylguanidine sulfate CAS 1185382-84-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1185382-84-6
Molecular FormulaC9H12FN3
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(2-Fluorobenzyl)-1-methylguanidine sulfate CAS 1185382-84-6 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 1-(2-Fluorobenzyl)-1-methylguanidine sulfate.

1-(2-Fluorobenzyl)-1-methylguanidine sulfate (CAS 1185382-84-6) is a high-purity analytical reference standard with the molecular formula C9H12FN3H2O4S and a molecular weight of 279.29 g/mol.

1-(2-Fluorobenzyl)-1-methylguanidine sulfate (C9H12FN3H2O4S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; 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.

As a certified reference material (CRM), 1-(2-Fluorobenzyl)-1-methylguanidine sulfate 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 FormulaC9H12FN3 H2O4S
Molecular Weight279.29 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentF-containing
Nitrogen Atoms3
Sulfur Atoms1

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