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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

9,11,13,15-Octadecatetraenoic acid

CC/C=CC=C/C=CC=CCCCCCCCC(=O)O Request for Quotation
Chemical Name: 9,11,13,15-Octadecatetraenoic acid
CAS Number: 18427-44-6
Product Number: AG00AQA2(AGN-PC-0JLG2W)
Synonyms:
MDL No:
Molecular Formula: C18H28O2
Molecular Weight: 276.4137

Identification/Properties

Computed Properties
Molecular Weight:
276.42g/mol
XLogP3:
5.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
12
Exact Mass:
276.209g/mol
Monoisotopic Mass:
276.209g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
335
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
4
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Parinaric acid, a fluorescent polyunsaturated fatty acid, finds essential applications in chemical synthesis as a versatile probe for studying lipid membranes and evaluating oxidative stress. Its unique properties make it a valuable tool in various research fields, including biochemistry, biophysics, and cell biology. By incorporating Parinaric acid into lipid bilayers, researchers can investigate membrane fluidity, lipid peroxidation, and membrane dynamics. Moreover, its sensitive fluorescence properties allow for real-time monitoring of lipid oxidation processes, making it a valuable tool for studying lipid metabolism and oxidative stress in cells. Additionally, Parinaric acid can serve as a molecular sensor to detect changes in membrane structure and lipid composition, providing insights into various biological processes. Its applications extend to the development of novel liposomal carriers for drug delivery and as a fluorescent label for studying lipid-protein interactions. By leveraging the unique properties of Parinaric acid in chemical synthesis, researchers can gain a deeper understanding of cellular membranes and oxidative stress mechanisms, paving the way for advancements in biomedical research and drug development.