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CAS

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69371-38-6

(5E,8Z,11Z,13Z)-15-hydroperoxyicosa-5,8,11,13-tetraenoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 69371-38-6 Structure

  • Basic information

    1. Product Name: (5E,8Z,11Z,13Z)-15-hydroperoxyicosa-5,8,11,13-tetraenoic acid
    2. Synonyms:
    3. CAS NO:69371-38-6
    4. Molecular Formula: C20H32O4
    5. Molecular Weight: 336.4657
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 69371-38-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 518°C at 760 mmHg
    3. Flash Point: 175.6°C
    4. Appearance: N/A
    5. Density: 1.013g/cm3
    6. Vapor Pressure: 6.75E-13mmHg at 25°C
    7. Refractive Index: 1.512
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (5E,8Z,11Z,13Z)-15-hydroperoxyicosa-5,8,11,13-tetraenoic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: (5E,8Z,11Z,13Z)-15-hydroperoxyicosa-5,8,11,13-tetraenoic acid(69371-38-6)
    12. EPA Substance Registry System: (5E,8Z,11Z,13Z)-15-hydroperoxyicosa-5,8,11,13-tetraenoic acid(69371-38-6)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 69371-38-6(Hazardous Substances Data)

69371-38-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69371-38-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,3,7 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 69371-38:
(7*6)+(6*9)+(5*3)+(4*7)+(3*1)+(2*3)+(1*8)=156
156 % 10 = 6
So 69371-38-6 is a valid CAS Registry Number.

69371-38-6Relevant articles and documents

Synthesis of phospholipids bearing a conjugated oxo-polyunsaturated fatty acid residue

Zhu, Changjin,Ohashi, Takaaki,Morimoto, Tatsuya,Onyango, Arnold N.,Takao, Kaneko,Shimizu, Sakayu,Nakajima, Shuhei,Baba, Naomichi

, p. 500 - 501 (1999)

2-(15'-Oxo-5',8',11',13'-eicosatetraenoyl)-1-stearoyl- sn- glycerol(3)phosphocholine (APC-CO) 1 and 2 and 2-(13'-oxo-9',11'- octadecadienoyl)-1-stearoyl-sn-glycero(3)phosphocholine (LPC-CO) 3 are synthesized and an analytical system established for the determination of geometrical isomers at the 13' position of APC-CO.

Physcomitrella patens has lipoxygenases for both eicosanoid and octadecanoid pathways

Anterola, Aldwin,G?bel, Cornelia,Hornung, Ellen,Sellhorn, George,Feussner, Ivo,Grimes, Howard

experimental part, p. 40 - 52 (2009/07/11)

Mosses have substantial amounts of long chain C20 polyunsaturated fatty acids, such as arachidonic and eicosapentaenoic acid, in addition to the shorter chain C18 α-linolenic and linoleic acids, which are typical substrates of lipoxygenases in flowering p

Iron-mediated generation of the neurotoxin 6-hydroxydopamine quinone by reaction of fatty acid hydroperoxides with dopamine: A possible contributory mechanism for neuronal degeneration in parkinson's disease

Pezzella, Alessandro,D'Ischia, Marco,Napolitano, Alessandra,Misuraca, Giovanna,Prota, Giuseppe

, p. 2211 - 2216 (2007/10/03)

Exposure of dopamine to an excess of linoleic acid 13-hydroperoxide (13- hydroperoxyoetadecadienoic acid) in the presence of ferrous ions in Tris buffer, pH 7.4, resulted in a relatively fast, oxygen-independent reaction exhibiting first-order kinetics wi

Unified Mechanism for Polyunsaturated Fatty Acid Autooxidation. Competition of Peroxy Radical Hydrogen Atom Abstraction, β-Scission, and Cyclization

Porter, Ned A.,Lehman, Laura S.,Weber, Bruce A.,Smith, Karl J.

, p. 6447 - 6455 (2007/10/02)

The autooxidation of linoleic (18:2) and arachidonic (20:4) acids with several cosubstrates was investigated.Cumene, tetralin, 1,4-cyclohexadiene, and 9,10-dihydroanthracene in benzene were used as cosubstrates for the oxidation of linoleic acid.The distribution of products, trans,cis diene hydroperoxides and trans,trans diene hydroperoxides, was dependent on the ability of cosubstrates to donate hydrogen atoms to linoleate peroxy radicals.Arachidonic acid was oxidized in mixtures of benzene/1,4-cyclohexadiene with linoleic acid internal standard.Product distribution of six hydroperoxyeicosatetraenoic acids (HPETE) derived from arachidonic acid was established at different concentrations of 1,4-cyclohexadiene in the solvent mixture.A kinetic expression is derived that is useful in describing polyunsaturated fatty acid oxidation product mixtures.By the use of this kinetic derivation, the rate of cyclization of peroxy free radicals derived from arachidonic acid was determined.

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