Loteprednol Impurity 16

N° de SZ CAT:	SZ-L034025
Número CAS	1402683-03-7
Mol.F.	C41H52O10
Peso Molecular	704.9
Status de Fatura	In Stock

Disclaimer

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 development or finding in product specification without further noticed.

Nome Químico: Methylene (8S,8'S,9S,9'S,10R,10'R,11S,11'S,13S,13'S,14S,14'S,17R,17'R)-bis(11,17-dihydroxy-10,13-dimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene-17-carboxylate)

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: C[C@]([C@@]1(O)C(OCOC([C@]([C@]2(C3)C)(CC[C@@]2([H])[C@@](CCC4=CC5=O)([H])[C@]([C@]4(C=C5)C)([H])[C@H]3O)O)=O)=O)(C6)[C@](CC1)([H])[C@@](CCC7=CC8=O)([H])[C@]([C@]7(C=C8)C)([H])[C@H]6O

Potential Use of Cyclodextrin Complexes for Enhanced Stability, Anti-inflammatory Efficacy, and Ocular Bioavailability of Loteprednol Etabonate
By Soliman, Osama Abd El-Aazeem; Mohamed, Elham Abdel Monem; El-Dahan, Marwa Salah; Khatera, Nabil Abdullah Ali
From AAPS PharmSciTech (2017), 18(4), 1228-1241

Determination of edetate disodium dihydrate in loteprednol and tobramycin ophthalmic suspension by RP-HPLC
By Xue, Qi; Yang, Longhua
From Zhongguo Yaoye (2012), 21(1), 24-25

An HPLC method to evaluate purity of a steroidal drug, loteprednol etabonate
By Yasueda, Shin-ichi; Higashiyama, Masayo; Shirasaki, Yoshihisa; Inada, Katsuhiro; Ohtori, Akira
From Journal of Pharmaceutical and Biomedical Analysis (2004), 36(2), 309-316

Loteprednol Impurity 16 is chemically Methylene (8S,8'S,9S,9'S,10R,10'R,11S,11'S,13S,13'S,14S,14'S,17R,17'R)-bis(11,17-dihydroxy-10,13-dimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene-17-carboxylate). Loteprednol Impurity 16 is supplied with detailed characterization data compliant with regulatory guideline. Loteprednol Impurity 16 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 Loteprednol.

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.

Loteprednol Impurity 16

Contacts

Our Locations