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Picture of Tacrolimus EP Impurity I

Tacrolimus EP Impurity I

SZ CAT No:SZ-T005003
CAS No
104987-16-8
Mol.F.
C44H67NO11
Mol.Wt.
786.0
Inv. Status
In Stock
Shipping Condition Ice Pack

Chemical Name: (3S,4R,5E,8R,9E,12S,14S,15R,16S,18R,19R,26aS)-19-hydroxy-3-[(1E)-1-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]prop-1-en-2-yl]-14,16-dimethoxy-4,10,12,18-tetramethyl-8-(prop-2-en-1-yl)-3,4,8,11,12,13,14,15,16,17,18,19,24,25,26,26a-hexadecahydro-7H-15,19-epoxypyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,20,21(23H)-tetrone (as per EP) ; (14E,18E)-17-Allyl-1-hydroxy-12-[(E)-2-(4-hydroxy-3-methoxycyclohexyl)-1-methylvinyl]-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9] octacosa-14,18-diene-2,3,10,16-tetrone (as per USP)

Synonym: Tacrolimus Diene (USP)

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Smiles: O[C@H]1[C@H](OC)C[C@H](/C=C(C)/[C@@H](OC([C@@H]2N(C(C([C@@]3(O)[C@H](C)C[C@H](OC)[C@]4([H])O3)=O)=O)CCCC2)=O)[C@H](C)/C=C/C([C@H](CC=C)/C=C(C[C@H](C)C[C@@H]4OC)\C)=O)CC1

Tacrolimus EP Impurity I is chemically (3S,4R,5E,8R,9E,12S,14S,15R,16S,18R,19R,26aS)-19-hydroxy-3-[(1E)-1-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]prop-1-en-2-yl]-14,16-dimethoxy-4,10,12,18-tetramethyl-8-(prop-2-en-1-yl)-3,4,8,11,12,13,14,15,16,17,18,19,24,25,26,26a-hexadecahydro-7H-15,19-epoxypyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,20,21(23H)-tetrone (as per EP) ; (14E,18E)-17-Allyl-1-hydroxy-12-[(E)-2-(4-hydroxy-3-methoxycyclohexyl)-1-methylvinyl]-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9] octacosa-14,18-diene-2,3,10,16-tetrone (as per USP). It is also known as Tacrolimus Diene (USP). Tacrolimus EP Impurity I is supplied with detailed characterization data compliant with regulatory guideline. Tacrolimus EP Impurity I 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 Tacrolimus.

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.

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