Duloxetine Impurity 7

SZ CAT No:	SZ-D001029
CAS No	494221-37-3
Mol.F.	C15H17NO2S2 : HCl
Mol.Wt.	307.4 : 36.5
Inv. Status	Custom Synthesis
Rel. CAS No	763079-11-4 (free base)

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Chemical Name: 3,3'-(methylazanediyl)bis(1-(thiophen-2-yl)propan-1-one) hydrochloride

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Smiles: O=C(C1=CC=CS1)CCN(C)CCC(C2=CC=CS2)=O.Cl

Characterization of impurities formed by interaction of duloxetine HCl with enteric polymers hydroxypropyl methylcellulose acetate succinate and hydroxypropyl methylcellulose phthalate
P J Jansen 1, P L Oren, C A Kemp, S R Maple, S W Baertschi
J Pharm Sci. 1998 Jan;87(1):81-5.

Analysis of Duloxetine Hydrochloride and Its Related Compounds in Pharmaceutical Dosage Forms and In Vitro Dissolution Studies by Stability Indicating UPLC
Dantu Durga Rao1,*, Shakil S. Sait1, A. Malleswara Reddy1, Dinesh Chakole1, Y. Ramakoti Reddy2, and K. Mukkanti
Journal of Chromatographic Science, Vol. 48, November/December 2010

Development and validation of a stability indicating rp-lc method for the estimation of process related impurities and degradation products of duloxetine hydrochloride and phthalic acid in duloxetine hydrochloride delayed release capsules
Navneet Kumar,1,2 D. Sangeetha,2 Bhupendrasinh Vaghela,1 P. Sunil Reddy,1 and Anuj Raghav
Journal of Liquid Chromatography & Related Technologies, 35:867–881, 2012

Determinationof Duloxetine and Its MajorMetabolites in Rabbit Plasma by High-Performance Liquid Chromatography
T. K. Laha1*, S. Sen1, G. Mishra
International Journal of Pharmaceutical Sciences and Drug Research 2015; 7(2): 176-181

Development and Validation of UPLC Method for the Determination of Duloxetine Hydrochloride and Its Impurities in Active Pharmaceutical Ingredient
Rohith T1 , Ananda S1,2*, Sajan PG2 and Gowda NM3
J Anal Bioanal Tech Volume 6, Issue 1

Duloxetine Impurity 7 is chemically 3,3'-(methylazanediyl)bis(1-(thiophen-2-yl)propan-1-one) hydrochloride. Duloxetine Impurity 7 is supplied with detailed characterization data compliant with regulatory guideline. Duloxetine Impurity 7 can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Duloxetine.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.

Duloxetine Impurity 7

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Mol.F.	: C10H9N
Mol.Wt.	: 143.2
Inv. Status	: In Stock

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Mol.F.	: C18H19NO2S : C2H4O2
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Inv. Status	: Custom Synthesis

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Mol.F.	: C19H21NO6S2
Mol.Wt.	: 423.5
Inv. Status	: Custom Synthesis

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Mol.F.	: C18H19NOS
Mol.Wt.	: 297.4
Inv. Status	: Under Synthesis

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Mol.F.	: C18H19NOS
Mol.Wt.	: 297.4
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Inv. Status	: Custom Synthesis

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Mol.Wt.	: 300.4
Inv. Status	: Custom Synthesis

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Mol.F.	: C18H14D5NOS
Mol.Wt.	: 302.5
Inv. Status	: Custom Synthesis

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Mol.F.	: C18H19NOS : HCl
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Mol.Wt.	: 339.5
Inv. Status	: In Stock

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CAS No	: 1243540-89-7
Mol.F.	: C19H19NO2S
Mol.Wt.	: 325.4
Inv. Status	: Custom Synthesis

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Mol.Wt.	: 423.6
Inv. Status	: Custom Synthesis

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Mol.Wt.	: 183.3
Inv. Status	: In Stock

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Mol.F.	: C8H11NO2S
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Inv. Status	: Custom Synthesis

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Inv. Status	: In Stock

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Inv. Status	: In Stock

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Mol.Wt.	: 200.3
Inv. Status	: In Stock

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Inv. Status	: Custom Synthesis

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