methyl 3-amino-4,5-dimethyl-1H-pyrrole-2-carboxylate CAS 1661860-81-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1661860-81-6
Molecular FormulaC8H12N2O2
Molecular Weight168.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

methyl 3-amino-4,5-dimethyl-1H-pyrrole-2-carboxylate CAS 1661860-81-6 chemical structure

Description

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.

CATO supplies methyl 3-amino-4,5-dimethyl-1H-pyrrole-2-carboxylate (CAS 1661860-81-6), a certified reference material (molecular formula C8H12N2O2, MW 168.19 g/mol) for analytical method development and quality control.

The molecular framework of methyl 3-amino-4,5-dimethyl-1H-pyrrole-2-carboxylate (C8H12N2O2) is characterized by an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

Physical & Chemical Properties

Molecular FormulaC8H12N2O2
Molecular Weight168.19 g/mol
AppearanceOff-white to pale yellow crystalline powder. (faint amine-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1993
Nitrogen Atoms2

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