Montelukast Dicyclohexylamine Salt Impurity

Also known as Montelukast racemate CRS, Montelukast DCHA, Montelukast racemate

CAS number
577953-88-9
Molecular formula
C47H59ClN2O3S
Molecular weight
767.5 g/mol
Catalogue number
OS-23467
Purity
≥ 99 %
Grade
Pharmaceutical (IP/BP/USP/EP), Reagent / Synthesis
Form
Powder
Packing
1 gm or 10 gm

₹40,000 per kg

Specifications

Identity
CAS number 577953-88-9
Molecular formula C47H59ClN2O3S
Molecular weight 767.5 g/mol
IUPAC name 2-[1-[[(1R)-1-[3-[(E)-2-(7-chloroquinolin-2-yl)ethenyl]phenyl]-3-[2-(2-hydroxypropan-2-yl)phenyl]propyl]sulfanylmethyl]cyclopropyl]acetic acid;N-cyclohexylcyclohexanamine
InChIKey ZLOLVGQQYDQBMP-HKHDRNBDSA-N
SMILES CC(C)(C1=CC=CC=C1CC[C@H](C2=CC=CC(=C2)/C=C/C3=NC4=C(C=CC(=C4)Cl)C=C3)SCC5(CC5)CC(=O)O)O.C1CCC(CC1)NC2CCCCC2
PubChem CID 16202490
Physical properties
Physical form Powder
Quality
Purity ≥ 99 %
Grade Pharmaceutical (IP/BP/USP/EP), Reagent / Synthesis
Packaging
Packaging size 1 gm or 10 gm
Packaging type Bottle
Storage
Storage Room Temperature
Pharmaceutical
API name montelukast
Commercial
Country of origin India

Description and applications

Montelukast Dicyclohexylamine salt is a known impurity (often referenced as EP Impurity G or DCHA salt) of the asthma drug Montelukast, characterized as a white powder, a salt formed between Montelukast acid and Dicyclohexylamine, used as a reference standard for method development, QC, and validation in pharmaceutical analysis, helping ensure the purity and safety of Montelukast drug products. Its structure combines the Montelukast molecule with Dicyclohexylamine, crucial for identifying and quantifying this specific impurity in API manufacturing. 

Applications

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