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ChemicalBook > Product Catalogue >Analytical Chemistry >Standard >Pharmaceutical Impurity Reference Standards >4-cyclohexyl-alpha-methylnaphthalene-1-acetic acid

4-cyclohexyl-alpha-methylnaphthalene-1-acetic acid

4-cyclohexyl-alpha-methylnaphthalene-1-acetic acid Structure
  • ₹18748.9
  • Product name: 4-cyclohexyl-alpha-methylnaphthalene-1-acetic acid
  • CAS: 71109-09-6
  • MF: C19H22O2
  • MW: 282.38
  • EINECS:275-196-6
  • MDL Number:MFCD00866019
  • Synonyms:4-cyclohexyl-alpha-methylnaphthalene-1-acetic acid ;Quadrisol;2-(4-Cyclohexil-1-naphthyl)-propionic Acid;4-Cyclohexyl-a-methyl-1-naphthaleneacetic Acid;CERM 10202;PM-150;4-Cyclohexyl-α-methyl-1-naphthaleneacetic acid;4-Cyclohexyl-α-Methyl-
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Selected condition:

Brand

  • Sigma-Aldrich(India)

Package

  • 10MG
  • ManufacturerSigma-Aldrich(India)
  • Product number32533
  • Product descriptionVedaprofen VETRANAL?, analytical standard
  • Packaging10MG
  • Price₹18748.9
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) 32533 Vedaprofen VETRANAL?, analytical standard 10MG ₹18748.9 2022-06-14 Buy

Properties

Melting point :150°C
Boiling point :465.9±14.0 °C(Predicted)
Density :1.132±0.06 g/cm3(Predicted)
storage temp. :-20°C Freezer
solubility :DMF: 25 mg/ml; DMSO: 10 mg/ml; Ethanol: 10 mg/ml
pka :4.90±0.30(Predicted)
form :Solid
color :White to off-white
BRN :5568831
EPA Substance Registry System :1-Naphthaleneacetic acid, 4-cyclohexyl-.alpha.-methyl- (71109-09-6)

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H302 Harmful if swallowed Acute toxicity,oral Category 4 Warning GHS hazard pictograms P264, P270, P301+P312, P330, P501
Precautionary statements:

Description

Vedaprofen is a non-steroidal anti-inflammatory drug (NSAID) commonly used in veterinary medicine to combat pain, inflammation, and fever associated with acute and chronic musculoskeletal disorders in horses and dogs. In addition to inhibiting COX and reducing prostaglandin H2 synthesis, vedaprofen is reported to block the activity of the E. coli DNA polymerase III β subunit, preventing DNA replication and repair.

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