Ibuprofen lysine, (-)-

Base Information

Chemical Name:Ibuprofen lysine, (-)-
CAS No.:157369-85-2
Molecular Formula:C₆H₁₄N₂O₂*C₁₃H₁₈O₂
Molecular Weight:352.474
Hs Code.:
UNII:5TQJ0240XA
DSSTox Substance ID:DTXSID50566909
Wikidata:Q27262855
Mol file:157369-85-2.mol

Synonyms:Ibuprofen lysine, (-)-;157369-85-2;(R)-(-)-Ibuprofen (S)-(+)-Lysinate;Ibuprofen L-lysine, (-)-;R-(-)-Ibuprofen L-lysine salt;UNII-5TQJ0240XA;5TQJ0240XA;(2S)-2,6-diaminohexanoic acid;(2R)-2-[4-(2-methylpropyl)phenyl]propanoic acid;L-Lysine, mono((R)-alpha-methyl-4-(2-methylpropyl)benzeneacetate);L-Lysine, mono((alphaR)-alpha-methyl-4-(2-methylpropyl)benzeneacetate);(R)-(-)-IBUPROFEN, (S)-(+)-LYSINATE;ibuprofen-lysine;(-)-ibuprofen lysine;SCHEMBL8579043;DTXSID50566909;PD132592;Q27262855;L-Lysine--(2R)-2-[4-(2-methylpropyl)phenyl]propanoic acid (1/1);L-Lysine compound with (R)-2-(4-isobutylphenyl)propanoic acid (1:1);L-LYSINE, MONO((.ALPHA.R)-.ALPHA.-METHYL-4-(2-METHYLPROPYL)BENZENEACETATE);L-LYSINE, MONO((R)-.ALPHA.-METHYL-4-(2-METHYLPROPYL)BENZENEACETATE)

Suppliers and Price of Ibuprofen lysine, (-)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
(R)-(-)-Ibuprofen(S)-(+)-Lysinate
250mg
$ 1110.00

Medical Isotopes, Inc.
(R)-(-)-Ibuprofen,(S)-(+)-Lysinate
50 mg
$ 1680.00

Medical Isotopes, Inc.
(R)-(-)-Ibuprofen,(S)-(+)-Lysinate
10 mg
$ 835.00

Total 3 raw suppliers

Chemical Property of Ibuprofen lysine, (-)-

Chemical Property:

Melting Point:185-187°C
PSA：126.64000
LogP:4.00110
Storage Temp.:Refrigerator
Solubility.:Methanol, Water
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:9
Exact Mass:352.23620751
Heavy Atom Count:25
Complexity:309

Purity/Quality:

99% ^*data from raw suppliers

(R)-(-)-Ibuprofen(S)-(+)-Lysinate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)CC1=CC=C(C=C1)C(C)C(=O)O.C(CCN)CC(C(=O)O)N
Isomeric SMILES:C[C@H](C1=CC=C(C=C1)CC(C)C)C(=O)O.C(CCN)C[C@@H](C(=O)O)N
Uses A nonsteroidal anti-inflammatory drug (NSAID). Optically active, selective cyclooxygenase inhibitor (IC50=14.9uM). Inhibits PGH synthase-1 and PGH synthase-2 with comparable potency

Technology Process of Ibuprofen lysine, (-)-

There total 11 articles about Ibuprofen lysine, (-)- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 84.0%