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Oxeladin EP Impurity C | CAS 101778-55-6 - Request Quote

Picture of Oxeladin EP Impurity C

Oxeladin EP Impurity C

SZ CAT No:SZ-O069004
CAS No
101778-55-6
Mol.F.
C18H29NO2
Mol.Wt.
291.4
Inv. Status
Synthesis on demand
Rel. CAS No3668-71-1 (HCl salt)
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    Usage Note:

    Oxeladin EP Impurity C is chemically 2-(Diethylamino)ethyl 2-ethyl-2-phenylbutanoate (as per EP). Oxeladin EP Impurity C is supplied with detailed characterization data compliant with regulatory guideline. Oxeladin EP Impurity C 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 Oxeladin.

    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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    • Mol.Wt.: 335.5 : 192.1
    • Inv. Status: Synthesis on demand
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    Oxeladin EP Impurity A

    • SZ CAT No: SZ-O069002
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    • Mol.F.: C8H19NO2
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    Oxeladin EP Impurity B

    • SZ CAT No: SZ-O069003
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    • Mol.Wt.: 192.3
    • Inv. Status: Synthesis on demand
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    Oxeladin EP Impurity C

    • SZ CAT No: SZ-O069004
    • CAS No:
      101778-55-6
    • Mol.F.: C18H29NO2
    • Mol.Wt.: 291.4
    • Inv. Status: Synthesis on demand
    • Rel. CAS No: 3668-71-1 (HCl salt)
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    Oxeladin EP Impurity D

    • SZ CAT No: SZ-O069005
    • CAS No:
      18109-80-3
    • Mol.F.: C18H29NO3
    • Mol.Wt.: 307.4
    • Inv. Status: In Stock
    • Rel. CAS No: 18109-81-4 (citrate salt)
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