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IBUPROFEN SODIUM SALT

IBUPROFEN SODIUM SALT Structure
IBUPROFEN SODIUM SALT
  • CAS No.31121-93-4
  • Chemical Name:IBUPROFEN SODIUM SALT
  • CBNumber:CB0116983
  • Molecular Formula:C13H17NaO2
  • Formula Weight:228.26
  • MOL File:31121-93-4.mol
IBUPROFEN SODIUM SALT Property
  • Melting point 110-112 °C
  • storage temp. Hygroscopic, -20°C Freezer, Under inert atmosphere
  • solubility H2O: 100 mg/mL, may be clear to slightly hazy
  • form Solid
  • color White to Off-White
  • Water Solubility H2O: 100mg/mL, clear to slightly hazy
  • Stability Stable. Incompatible with strong oxidizing agents
  • CAS DataBase Reference 31121-93-4
  • EWG's Food Scores 1
  • FDA UNII O0PJ4UZ01U
  • UNSPSC Code 41116107
  • NACRES NA.24
Safety
  • Safety Statements  :22-24/25
  • WGK Germany  :3
  • RTECS  :MU6641000
Hazard and Precautionary Statements (GHS)
  • Symbol(GHS)
  • Signal wordWarning
  • Hazard statements H319-H302-H335
  • Precautionary statements P264-P270-P301+P312-P330-P501-P264-P280-P305+P351+P338-P337+P313P
IBUPROFEN SODIUM SALT Price More Price(2)
  • Brand: Sigma-Aldrich(India)
  • Product number: I1892
  • Product name : Ibuprofen sodium salt
  • Purity: analytical standard, ≥98% (GC)
  • Packaging: 100G
  • Price: ₹17677.23
  • Updated: 2022/06/14
  • Buy: Buy
  • Brand: Sigma-Aldrich(India)
  • Product number: I1892
  • Product name : Ibuprofen sodium salt
  • Purity: analytical standard, ≥98% (GC)
  • Packaging: 500G
  • Price: ₹62752.53
  • Updated: 2022/06/14
  • Buy: Buy

IBUPROFEN SODIUM SALT Chemical Properties,Usage,Production

  • Chemical Properties white powder
  • Uses Ibuprofen ((±)-Ibuprofen) sodium is an orally active, selective COX-1 inhibitor with an IC50 value of 13 μM. Ibuprofen sodium inhibits cell proliferation, angiogenesis, and induces cell apoptosis. Ibuprofen sodium is a nonsteroidal anti-inflammatory agent and a nitric oxide (NO) donor. Ibuprofen sodium can be used in the research of pain, swelling, inflammation, infection, immunology, cancers[1][2][5][8].
  • Application Ibuprofen sodium salt is a useful research chemical.
  • Biological Activity Cyclooxygenase (COX) inhibitor th at has greater activity against COX-1 than against COX-2.
  • in vivo

    Ibuprofen sodium (fed in animal feedings, 300 mg/kg, 14 days) reduces overall tumor growth and enhances anti-tumor immune characteristics without adverse autoimmune reactions in a model of postpartum breast cancer[5].
    Ibuprofen sodium (subcutaneous injection, 60 mg/kg, every second day for 15 days) reduces the risk of neuropathy in a rat model of chronic Oxaliplatin?induced peripheral neuropathy[6].
    Ibuprofen sodium (oral administration, 20 mg/kg, every 12 hours, 5 doses total) decreases muscle growth (average muscle fiber cross-sectional area) without affecting regulation of supraspinatus tendon adaptions to exercise[7].
    Ibuprofen sodium (oral administration, 35 mg/kg, twice daily) attenuates the Inflammatory response to pseudomonas aeruginosa in a rat model of chronic pulmonary infection[8].

    Animal Model:Syngeneic (D2A1) orthotopic Balb/c mouse model of PPBC (postpartum)[5]
    Dosage:300 mg/kg, daily for 14 days
    Administration:Fed in animal feedings (added to pulverized standard chow and mixed dry, then mixed with water, made into chow pellets and dried thoroughly)
    Result:Suppresed tumor growth, reduced presence of immature monocytes and increased numbers of T cells.
    Enhanced Th1 associated cytokines as well as promoted tumor border accumulation of T cells.
    Animal Model:Oxaliplatin?induced peripheral neuropathy[6]
    Dosage:60 mg/kg, every second day for 15 days
    Administration:Subcutaneous injection
    Result:Lowered sensory nerve conduction velocity (SNCV).
  • IC 50 COX-1: 13 μM (IC50); COX-2: 370 μM (IC50)
  • References [1] Noreen Y, et al. Development of a radiochemical cyclooxygenase-1 and -2 in vitro assay for identification of natural products as inhibitors of prostaglandin biosynthesis. J Nat Prod. 1998 Jan;61(1):2-7. DOI:10.1021/np970343j
    [2] Hassan Akrami, et al. Inhibitory effect of ibuprofen on tumor survival and angiogenesis in gastric cancer cell. Tumour Biol. 2015 May;36(5):3237-43. DOI:10.1007/s13277-014-2952-3
    [3] Sharon M Rymut, et al. Ibuprofen regulation of microtubule dynamics in cystic fibrosis epithelial cells. Am J Physiol Lung Cell Mol Physiol. 2016 Aug 1;311(2):L317-27. DOI:10.1152/ajplung.00126.2016
    [4] Emmanuelle Bignon, et al. Ibuprofen and ketoprofen potentiate UVA-induced cell death by a photosensitization process. Sci Rep. 2017 Aug 21;7(1):8885. DOI:10.1038/s41598-017-09406-8
    [5] Nathan D Pennock, et al. Ibuprofen supports macrophage differentiation, T cell recruitment, and tumor suppression in a model of postpartum breast cancer. J Immunother Cancer. 2018 Oct 1;6(1):98. DOI:10.1186/s40425-018-0406-y
    [6] Thomas Kr?ig?rd, et al. Protective effect of ibuprofen in a rat model of chronic oxaliplatin-induced peripheral neuropathy. Exp Brain Res. 2019 Oct;237(10):2645-2651. DOI:10.1007/s00221-019-05615-x
    [7] Sarah Ilkhanipour Rooney, et al. Ibuprofen Differentially Affects Supraspinatus Muscle and Tendon Adaptations to Exercise in a Rat Model. Am J Sports Med. 2016 Sep;44(9):2237-45. DOI:10.1177/0363546516646377
    [8] M W Konstan, et al. Ibuprofen attenuates the inflammatory response to Pseudomonas aeruginosa in a rat model of chronic pulmonary infection. Implications for antiinflammatory therapy in cystic fibrosis. Am Rev Respir Dis. 1990 Jan;141(1):186-92. DOI:10.1164/ajrccm/141.1.186
IBUPROFEN SODIUM SALT Preparation Products And Raw materials
Raw materials
Preparation Products
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IBUPROFEN SODIUM SALT Spectrum
31121-93-4, IBUPROFEN SODIUM SALTRelated Search:
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  • 原料药
  • 医药原料药-科研原料
  • Analytical Standards
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  • Analytical Chromatography Product Catalog
  • C13H17NaO2
  • C13H17O2Na
  • C13H18O2Na
  • 二水合布洛芬钠
  • 化合物 IBUPROFEN SODIUM
  • 2-(4-异丁基苯基)丙酸钠
  • 布洛芬钠
  • 布洛芬 钠盐
  • 苯乙酸, A-甲基-4-(2-甲基丙基)-,钠盐
  • 31121-93-4
  • (±)-Ibuprofen-d3 (sodium salt)
  • sodium,2-[4-(2-methylpropyl)phenyl]propanoate
  • (+/-)-Ibuprofen-d3, Sodium Salt (a-methyl-d3)
  • Benzeneacetic acid, a-Methyl-4-(2-Methylpropyl)-,sodiuM salt
  • Sodium ibuprofen
  • Hydratropic acid, p-isobutyl-, sodium salt
  • Einecs 250-477-6
  • Benzeneacetic acid, alpha-methyl-4-(2-methylpropyl)-, sodium salt (9ci)
  • 2-(p-Isobutylphenyl)propionic acid sodium salt
  • 2-(4-Isobutylphenyl)propionic acid sodium salt
  • sodiuM 2-(4-isobutylphenyl)propanoate
  • (±)-Ibuprofen-d3, SodiuM Salt
  • α-methyl-4-(isobutyl)phenylacetic acid
  • sodium 2-(4-isobutylphenyl)propionate
  • p-isobutyl-hydratropicacisodiumsalt
  • ALPHA-METHYL-4-(ISOBUTYL)PHENYLACETIC ACID SODIUM SALT
  • ALPHA-METHYL-4-[2-METHYLPROPYL]BENZENEACETIC ACID SODIUM SALT
  • p-isobutylhydratropicacidsodiumsalt
  • ibuprofensodium
  • alpha-methyl-4-(2-methylpropyl)-benzeneaceticacisodiumsalt
  • IBUPROFEN SODIUM SALT