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ChemicalBook > Product Catalogue >API >Antineoplastic agents >Hormonal antineoplastic drugs >Nilutamide

Nilutamide

Nilutamide Structure
  • ₹9677.55
  • Product name: Nilutamide
  • CAS: 63612-50-0
  • MF: C12H10F3N3O4
  • MW: 317.22
  • EINECS:
  • MDL Number:MFCD00864670
  • Synonyms:5,5-Dimethyl-3-[4-nitrcr3-(trifluoromethyl)phenyl]-2,4-imidazolidinedione;1-3-Trifluoromethyl-4-nitrophenyl)-4,4-dimethylimidazoline-2,5-dione;5,5-Dimethyl-3-[4-nitro-3-(trifluoromethyl)phenyl]-2,4-imidazolidinedion;Nilandron;Nilandrone;RU 23908-10;3-(3-(trifluoromethyl)-4-nitrophenyl)-5,5-dimethylimidazolidine-2,4-dione;2,4-Imidazolidinedione, 5,5-dimethyl-3-(4-nitro-3-(trifluoromethyl)phenyl)-
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Selected condition:

Brand

  • Sigma-Aldrich(India)

Package

  • 1G
  • ManufacturerSigma-Aldrich(India)
  • Product numberN8534
  • Product descriptionNilutamide solid
  • Packaging1G
  • Price₹9677.55
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) N8534 Nilutamide solid 1G ₹9677.55 2022-06-14 Buy

Properties

Melting point :1490C
Density :1.463±0.06 g/cm3(Predicted)
storage temp. :Sealed in dry,Room Temperature
solubility :Very slightly soluble in water, freely soluble in acetone, soluble in anhydrous ethanol.
form :solid
pka :7.59±0.70(Predicted)
color :Light yellow to yellow
InChIKey :XWXYUMMDTVBTOU-UHFFFAOYSA-N
CAS DataBase Reference :63612-50-0(CAS DataBase Reference)

Safety Information

Symbol(GHS): GHS hazard pictogramsGHS hazard pictograms
Signal word: Danger
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H301 Toxic if swalloed Acute toxicity,oral Category 3 Danger GHS hazard pictograms P264, P270, P301+P310, P321, P330,P405, P501
H360 May damage fertility or the unborn child Reproductive toxicity Category 1A, 1B Danger GHS hazard pictograms
Precautionary statements:
P201 Obtain special instructions before use.

Description

Nilutamide is a non-steroidal and silent androgen receptor inhibitor. Nilutamide binds to androgen receptors and also inhibits androgen biosynthesis in vitro.

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