Chlorprothixene EP Impurity E (Free Base)
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Includes: HPLC, MASS/LC-MS, 1H NMR, FT-IR, Potency, Structure Elucidation Report (SER), and additional analytical data depending on the product.

86-39-5Chlorprothixene EP Impurity E (Free Base)

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Catalogue No.:VE0017850
CAS No.:86-39-5
Mol. Formula:C13H7ClOS
Mol. Weight:246.7 g/mol

Additional information on CAS 86-39-5

Parent drug

Chlorprothixene

IUPAC Name

2-chloro-9H-thioxanthen-9-one

Pharmacopeial Synonyms

N/A

Other Synonyms

2-Chlorothioxanthen-9-one; 2-Chlorothioxanthone

Smiles

O=C1C2=C(SC3=C1C=CC=C3)C=CC(Cl)=C2

InChI

InChI=1S/C13H7ClOS/c14-8-5-6-12-10(7-8)13(15)9-3-1-2-4-11(9)16-12/h1-7H

Shipping Condition

Ambient Temperature

Description

Chlorprothixene EP Impurity E (Free Base), CAS 86-39-5, also known as 2-Chlorothioxanthen-9-one or 2-Chlorothioxanthone, is a process-related impurity arising from thioxanthone core transformations during chlorprothixene synthesis. This impurity exhibits a characteristic UV absorbance and increased retention in reversed-phase HPLC and can be definitively identified and quantified using LC-MS and 1H and 13C NMR spectroscopic data. Control of Impurity E is critical for API quality because its physicochemical properties can influence crystallization, assay reproducibility, and stability profiles. Analytical methods should be validated for specificity, sensitivity and robustness to satisfy ICH Q3A and relevant pharmacopeial requirements.

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