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ChemicalBook--->CAS DataBase List--->31121-93-4

31121-93-4

31121-93-4 Structure

31121-93-4 Structure
IdentificationBack Directory
[Name]

IBUPROFEN SODIUM SALT
[CAS]

31121-93-4
[Synonyms]

ibuprofensodium
Einecs 250-477-6
Sodium ibuprofen
IBUPROFEN SODIUM SALT
(±)-Ibuprofen-d3, SodiuM Salt
p-isobutylhydratropicacidsodiumsalt
p-isobutyl-hydratropicacisodiumsalt
sodium 2-(4-isobutylphenyl)propionate
sodiuM 2-(4-isobutylphenyl)propanoate
α-methyl-4-(isobutyl)phenylacetic acid
Hydratropic acid, p-isobutyl-, sodium salt
2-(4-Isobutylphenyl)propionic acid sodium salt
2-(p-Isobutylphenyl)propionic acid sodium salt
ALPHA-METHYL-4-(ISOBUTYL)PHENYLACETIC ACID SODIUM SALT
alpha-methyl-4-(2-methylpropyl)-benzeneaceticacisodiumsalt
Benzeneacetic acid, a-Methyl-4-(2-Methylpropyl)-,sodiuM salt
ALPHA-METHYL-4-[2-METHYLPROPYL]BENZENEACETIC ACID SODIUM SALT
Benzeneacetic acid, alpha-methyl-4-(2-methylpropyl)-, sodium salt (9ci)
[EINECS(EC#)]

250-477-6
[Molecular Formula]

C13H17NaO2
[MDL Number]

MFCD00133414
[MOL File]

31121-93-4.mol
[Molecular Weight]

228.26
Chemical PropertiesBack Directory
[Appearance]

white powder
[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 ]

neat
[color ]

White to Off-White
[Stability:]

Stable. Incompatible with strong oxidizing agents
[Water Solubility ]

H2O: 100mg/mL, clear to slightly hazy
[CAS DataBase Reference]

31121-93-4
Hazard InformationBack Directory
[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)
[storage]

4°C, away from moisture
[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
Safety DataBack Directory
[Safety Statements ]

22-24/25
[WGK Germany ]

3
[RTECS ]

MU6641000
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