Escitalopram

Escitalopram Structure
CAS No.
128196-01-0
Chemical Name:
Escitalopram
Synonyms
Seroplex;Escitalopram;Escitalopram CRS;EscitalopraM Oxalate INN;Escitalopram Impurity 31;(S)-(+)-CITALOPRAM OXALATE;(+)-(S)-Citalopram Oxalate;(+)-(S)-Citalopram-d4 Oxalate;Escitalopram oxalate impurity III;Escitalopram(Escitalopram Oxalate)
CBNumber:
CB2712918
Molecular Formula:
C20H21FN2O
Molecular Weight:
324.39
MOL File:
128196-01-0.mol
MSDS File:
SDS
Modify Date:
2024/11/16 15:32:52

Escitalopram Properties

alpha D +12.33° (c = 1 in methanol)
Boiling point 428.3±45.0 °C(Predicted)
Density 1.18±0.1 g/cm3(Predicted)
storage temp. 2-8°C
solubility Soluble in DMSO
form Powder
pka 9.57±0.28(Predicted)
color Off-white to light yellow
CAS DataBase Reference 128196-01-0(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H317-H302
Precautionary statements  P261-P272-P280-P302+P352-P333+P313-P321-P363-P501-P264-P270-P301+P312-P330-P501
NFPA 704
3
2 0

Escitalopram Chemical Properties,Uses,Production

Uses

antidepressive;selective serotonin reuptake inhibitor

Definition

ChEBI: A 1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-2-benzofuran-5-carbonitrile that has S-configuration at the chiral centre. It is the active enantiomer of citalopram.

Mechanism of action

Escitalopram is the S-enantiomer of citalopram that binds with high affinity and selectivity to the human SERT equivalent to (±)-citalopram. It has been reported that nearly all the activity resides in the S-enantiomer and that R-citalopram actually counteracts the action of the S-enantiomer. Studies show that escitalopram exhibits twice the activity of citalopram and is at least 27 times more potent than the R-enantiomer. The R-enantiomer inhibits the S-enantiomer at the transporter. Escitalopram's mechanism of action is common to the SSRIs.

Pharmacokinetics

The pharmacokinetics for escitalopram does not exhibit stereoisomer selectivity and, therefore, is similar to that for citalopram. Likewise, it exhibits linear pharmacokinetics so that plasma levels increase proportionately and predictably with increased doses, and its half-life of 27 to 32 hours is consistent with once-daily dosing. It also has been found that R-citalopram is cleared more slowly than the S-enantiomer. Therefore, when the drug is used as a racemic mixture (citalopram), the inactive isomer predominates at steady state. This is an added incentive for use of the enantiomerically pure escitalopram. Escitalopram has negligible effects on CYP isoforms, suggesting a low potential for drug–drug interactions. Escitalopram is indicated for patients with major depressive disorder, generalized anxiety disorder, panic disorder, and social anxiety disorder.

Escitalopram Preparation Products And Raw materials

Raw materials

Preparation Products

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Escitalopram Spectrum

(1R)-1-(3-dimethylaminopropyl)-1-(4-fluorophenyl)-3H-isobenzofuran-5-carbonitrile 1-(3-Dimethylaminopropyl)-1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-5-carbonitrile (S)-(+)-CITALOPRAM OXALATE Escitalopram (S)-CITALOPRAM S-(+)-1-3-(diMethyl-aMino) propyl-1-(p-fluorophenyl)-5-phthalancarbonitrile EscitalopraM Oxalate INN Seroplex S-(+)-1-3-(dimethyl-amino) propyl-1-(p-fluorophenyl)-5-phthalancarbonitrile Escitalopram(Escitalopram Oxalate) Escitalopram CRS 5-Isobenzofurancarbonitrile, 1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-, (1S)- Escitalopram oxalate impurity III Escitalopram Impurity 31 EscitalopramQ: What is Escitalopram Q: What is the CAS Number of Escitalopram Q: What is the storage condition of Escitalopram (1S)‐1‐[3‐ (dimethylamino)propyl]‐1‐(4‐ fluorophenyl)‐3H‐2‐benzofuran‐ 5‐carbonitrile?(CTS‐II?Base) (+)-(S)-Citalopram-d4 Oxalate (S)-1-(3-(Dimethylamino)propyl)-1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-5-carbonitrile (Escitalopram Impurity) (+)-(S)-Citalopram Oxalate 128196-01-0 128196-01-1 API