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.
Chemical Name: (8R,9S,13S,14S,17S)-3-Hydroxy-13-methyl-7-(9-((methylsulfonyl)oxy)nonyl)-8,9,12,13,14,15,16,17-octahydro-11H-cyclopenta[a]phenanthren-17-yl acetate
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
Smiles: C[C@@]12[C@](CC[C@@H]2OC(C)=O)([H])[C@]3([H])C(CCCCCCCCCO[S](C)(=O)=O)=CC4=CC(O)=CC=C4[C@@]3([H])CC1
Quantitative estimation of Fulvestrant injection 505(j) composition and impurities profile by capillary gas chromatography and HPLC-PDA techniquesBy Dongala, Thirupathi; Katari, Naresh Kumar; Marisetti, Vishnu Murthy; Jonnalagadda, Sreekantha B.From Journal of the Iranian Chemical Society (2021), 18(6), 1443-1454 Development and validation of HPLC-UV method for the estimation of fulvestrant in bulk drugBy Thummaluru, Rama Mohan Reddy; Gurrala, SrikanthFrom Journal of Pharmacy Research (Mohali, India) (2016), 10(1), 21-24 Stability indicating HPLC method for the determination of fulvestrant in pharmaceutical formulation in comparison with linear sweep voltammetric methodBy Atila, Alptug; Yilmaz, Bilal; Kadioglu, YucelFrom Iranian Journal of Pharmaceutical Research (2016), 15(3), 369-378
Fulvestrant Impurity 4 is chemically (8R,9S,13S,14S,17S)-3-Hydroxy-13-methyl-7-(9-((methylsulfonyl)oxy)nonyl)-8,9,12,13,14,15,16,17-octahydro-11H-cyclopenta[a]phenanthren-17-yl acetate. Fulvestrant Impurity 4 is supplied with detailed characterization data compliant with regulatory guideline. Fulvestrant Impurity 4 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 Fulvestrant.
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.
Fulvestrant
Fulvestrant EP Impurity A
Fulvestrant EP Impurity B
Fulvestrant EP Impurity C
Fulvestrant EP Impurity D
Fulvestrant EP Impurity E
Fulvestrant EP Impurity F
Fulvestrant Impurity 8 FV
Fulvestrant-3-Glucuronide
Fulvestrant-17-Glucuronide
Fulvestrant-3-Sulfate
17-Keto Fulvestrant
Fulvestrant Side Chain Impurity
Fulvestrant Impurity 1
Fulvestrant Impurity 2
Fulvestrant Impurity 3
Fulvestrant Impurity 4
Fulvestrant Chlora BANA
Fulvestrant intermediat-TBDMS Chain
Pentafluoro Pentanethiol
Fulvestrant D3
Fulvestrant D4
Fulvestrant Impurity 5
Fulvestrant Bromo Analogue Impurity 1
Fulvestrant Impurity 7
Fulvestrant Impurity 8
Fulvestrant Impurity 9
Fulvestrant Impurity 10
Fulvestrant Impurity 11
Fulvestrant Impurity 13
Fulvestrant Impurity 6 Free Base
Fulvestrant Impurity 12
Fulvestrant Impurity 14
Fulvestrant Impurity 15
Fulvestrant Impurity 16
Fulvestrant Impurity 17
Fulvestrant Impurity 18
Fulvestrant Impurity 19
Fulvestrant Impurity 20
Fulvestrant Impurity 21
Fulvestrant Impurity 22
Fulvestrant Impurity 23
Fulvestrant Dibromo Analogue Impurity
Fulvestrant Impurity 24
Delta (6,7) Deoxo Fulvestrant Impurity
Fulvestrant Impurity 26
S-Deoxo Fulvestrant
Fulvestrant R Enantiomer
Fulvestrant S Enantiomer
Fulvestranr Enantiomer