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IBUPROFEN SODIUM SALT

CAS No.
31121-93-4
Chemical Name:
IBUPROFEN SODIUM SALT
Synonyms
ibuprofensodium;Einecs 250-477-6;Sodium ibuprofen;IBUPROFEN SODIUM SALT;(±)-Ibuprofen-d3, SodiuM Salt;(±)-Ibuprofen-d3 (sodium salt);p-isobutylhydratropicacidsodiumsalt;p-isobutyl-hydratropicacisodiumsalt;sodiuM 2-(4-isobutylphenyl)propanoate;sodium 2-(4-isobutylphenyl)propionate
CBNumber:
CB0116983
Molecular Formula:
C13H17NaO2
Molecular Weight:
228.26
MDL Number:
MFCD00133414
MOL File:
31121-93-4.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-15 13:06:51
Product description Number Pack Size Price
Ibuprofen sodium salt analytical standard, ≥98% (GC) I1892 100g $205
Ibuprofen sodium salt analytical standard, ≥98% (GC) I1892 500g $756
Ibuprofen sodium ≥98% CS-0031024 500mg $60
Ibuprofen sodium ≥98% CS-0031024 1g $71
Ibuprofen sodium ≥98% CS-0031024 500mg $60

IBUPROFEN SODIUM SALT Properties

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
Major Application forensics and toxicology
pharmaceutical (small molecule)
InChI 1S/C13H18O2.Na/c1-9(2)8-11-4-6-12(7-5-11)10(3)13(14)15;/h4-7,9-10H,8H2,1-3H3,(H,14,15);/q;+1/p-1
InChIKey PTTPUWGBPLLBKW-UHFFFAOYSA-M
SMILES [Na+].CC(C)Cc1ccc(cc1)C(C)C([O-])=O
CAS DataBase Reference 31121-93-4
EWG's Food Scores 1
FDA UNII O0PJ4UZ01U
UNSPSC Code 41116107
NACRES NA.24

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H319-H302-H335
Precautionary statements  P264-P270-P301+P312-P330-P501-P264-P280-P305+P351+P338-P337+P313P
PPE Eyeshields, Gloves, type N95 (US)
Safety Statements  22-24/25
WGK Germany  3
RTECS  MU6641000
Storage Class 11 - Combustible Solids

IBUPROFEN SODIUM SALT price More Price(11)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich I1892 Ibuprofen sodium salt analytical standard, ≥98% (GC) 31121-93-4 100g $205 2026-04-30 Buy
Sigma-Aldrich I1892 Ibuprofen sodium salt analytical standard, ≥98% (GC) 31121-93-4 500g $756 2026-04-30 Buy
ChemScene CS-0031024 Ibuprofen sodium ≥98% 31121-93-4 500mg $60 2026-06-04 Buy
ChemScene CS-0031024 Ibuprofen sodium ≥98% 31121-93-4 1g $71 2026-06-04 Buy
ChemScene CS-0031024 Ibuprofen sodium ≥98% 31121-93-4 500mg $60 2026-06-04 Buy
Product number Packaging Price Buy
I1892 100g $205 Buy
I1892 500g $756 Buy
CS-0031024 500mg $60 Buy
CS-0031024 1g $71 Buy
CS-0031024 500mg $60 Buy

IBUPROFEN SODIUM SALT Chemical Properties,Uses,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 Oxaliplatininduced 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:Oxaliplatininduced 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 Krigrd, 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

IBUPROFEN SODIUM SALT Suppliers

Global( 79)Suppliers
Supplier Tel Email Country ProdList Advantage
Shaanxi Dideu Medichem Co. Ltd
+86-029-81138252 +86-173 9270 1263 1057@dideu.com China 3959 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21585 55
RongNa Biotechnology Co.,Ltd
+86-86-13583358881 +8618560316533 Brad@rongnabiotech.com China 3373 58
AFINE CHEMICALS LIMITED
+86-571-85134551 info@afinechem.com China 15080 58
HANGZHOU LEAP CHEM CO., LTD.
+86-571-87711850 market18@leapchem.com China 24597 58
Nantong HI-FUTURE Biology Co., Ltd.
+undefined18051384581 sales@chemhifuture.com China 3135 58
Dingwang Technology (Wuhan) Co., Ltd.
+undefined-27-2786652399 +undefined13627115097 market02@senwayer.com China 887 58
Shanghai Acmec Biochemical Technology Co., Ltd.
+86-18621343501; +undefined18621343501 product@acmec-e.com China 33324 58
Aladdin Scientific
tp@aladdinsci.com United States 52923 58
TargetMol Chemicals Inc.
+17819995354 marketing@targetmol.com United States 19956 58

View Lastest Price from IBUPROFEN SODIUM SALT manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Ibuprofen sodium pictures 2026-07-15 Ibuprofen sodium
31121-93-4
10g TargetMol Chemicals Inc.
IBUPROFEN SODIUM SALT pictures 2026-07-15 IBUPROFEN SODIUM SALT
31121-93-4
0.99 RongNa Biotechnology Co.,Ltd
IBUPROFEN SODIUM SALT pictures 2025-08-22 IBUPROFEN SODIUM SALT
31121-93-4
1kg 99% 500kg Dingwang Technology (Wuhan) Co., Ltd.

IBUPROFEN SODIUM SALT Spectrum

IBUPROFEN SODIUM SALT alpha-methyl-4-(2-methylpropyl)-benzeneaceticacisodiumsalt ibuprofensodium p-isobutylhydratropicacidsodiumsalt ALPHA-METHYL-4-[2-METHYLPROPYL]BENZENEACETIC ACID SODIUM SALT ALPHA-METHYL-4-(ISOBUTYL)PHENYLACETIC ACID SODIUM SALT p-isobutyl-hydratropicacisodiumsalt sodium 2-(4-isobutylphenyl)propionate α-methyl-4-(isobutyl)phenylacetic acid (±)-Ibuprofen-d3, SodiuM Salt sodiuM 2-(4-isobutylphenyl)propanoate 2-(4-Isobutylphenyl)propionic acid sodium salt 2-(p-Isobutylphenyl)propionic acid sodium salt Benzeneacetic acid, alpha-methyl-4-(2-methylpropyl)-, sodium salt (9ci) Einecs 250-477-6 Hydratropic acid, p-isobutyl-, sodium salt Sodium ibuprofen Benzeneacetic acid, a-Methyl-4-(2-Methylpropyl)-,sodiuM salt (+/-)-Ibuprofen-d3, Sodium Salt (a-methyl-d3) sodium,2-[4-(2-methylpropyl)phenyl]propanoate (±)-Ibuprofen-d3 (sodium salt) 31121-93-4 C13H18O2Na C13H17O2Na C13H17NaO2 Analytical Chromatography Product Catalog Alphabetic Analytical Standards