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Labetalol EP Impurity F (HCl salt) | CAS 96441-14-4 - Request Quote

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Labetalol EP Impurity F (HCl salt)

SZ CAT No:SZ-L007035
CAS No
96441-14-4
Mol.F.
C19H22N2O3
Mol.Wt.
326.4
Inv. Status
Under QC Approval
Rel. CAS No85665-85-6 (free base)

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Usage Note:

Labetalol EP Impurity F (HCl salt) is chemically 2-Hydroxy-5-[2-[[(2RS)-4-phenylbutan-2-yl]amino]acetyl]benzamide hydrochloride (as per EP) ; 2-Hydroxy-5-[(4-phenylbutan-2-yl)glycyl]benzamide hydrochloride (as per USP). It is also known as Labetalol USP Related Compound F ; Labetalol Keto Impurity ; Labetalone. Labetalol EP Impurity F (HCl salt) is supplied with detailed characterization data compliant with regulatory guideline. Labetalol EP Impurity F (HCl salt) 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 Labetalol.

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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Labetalol EP Impurity F (HCl salt) for Method Validation

Labetalol Reference Standard

Labetalol EP Impurity F (HCl salt) for ANDA Filing

Labetalol EP Impurity F (HCl salt) for Forced Degradation Studies

Labetalol EP Impurity F (HCl salt) Identification Standards

Labetalol EP Impurity F (HCl salt) for DMF Filing

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SynZeal product information given on this website is as per the existing understanding while publishing the details on website. The customer is responsible for assessing the accuracy of the information at the time of actual purchase.

SynZeal will update these details as per new developments or findings in product specifications without further notice.

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