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10015-85-7

Lecithindioleoyl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 10015-85-7 Structure

  • Basic information

    1. Product Name: Lecithindioleoyl
    2. Synonyms: 1,2-Dioleoylglycerophosphocholine;1,2-Docpc;1,2-Oleoyl-sn-glycero-3-phosphocholine;3,5,9-Trioxa-4-phosphaheptacos-18-en-1-aminium, 4-hydroxy-N,N,N-trimethyl-10-oxo-7-(((9Z)-1-oxo-9-octadecenyl)oxy)-, inner salt, 4-oxide, (18Z)-;Dielaidinoyl lecithin;1,2-oleoylphosphatidylcholine;(Z,Z)-4-Hydroxy-N,N,N-trimethyl-10-oxo-7-((1-oxo-9-octadecenyl)oxy)-3,5,9-trioxa-4-phosphaheptacos-18-en-1-aminium, hydroxide, inner salt, 4-oxide;1,2-Dioleoyl glycerophosphocholine
    3. CAS NO:10015-85-7
    4. Molecular Formula: C44H84NO8P
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10015-85-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Lecithindioleoyl(CAS DataBase Reference)
    10. NIST Chemistry Reference: Lecithindioleoyl(10015-85-7)
    11. EPA Substance Registry System: Lecithindioleoyl(10015-85-7)

  • 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: 10015-85-7(Hazardous Substances Data)

10015-85-7 Usage

Definition

ChEBI: A phosphatidylcholine in which the phosphatidyl acyl groups are both oleoyl.

Check Digit Verification of cas no

The CAS Registry Mumber 10015-85-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,1 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10015-85:
(7*1)+(6*0)+(5*0)+(4*1)+(3*5)+(2*8)+(1*5)=47
47 % 10 = 7
So 10015-85-7 is a valid CAS Registry Number.
InChI:InChI=1/C44H84NO8P/c1-6-8-10-12-14-16-18-20-22-24-26-28-30-32-34-36-43(46)50-40-42(41-52-54(48,49)51-39-38-45(3,4)5)53-44(47)37-35-33-31-29-27-25-23-21-19-17-15-13-11-9-7-2/h20-23,42H,6-19,24-41H2,1-5H3/b22-20-,23-21-

10015-85-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name dioleoyl phosphatidylcholine

1.2 Other means of identification

Product number -
Other names phosphatidylglycholine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10015-85-7 SDS

10015-85-7Relevant articles and documents

cis-trans Isomerization of monounsaturated fatty acid residues in phospholipids by thiyl radicals

Chatgilialoglu, Chryssostomos,Ferreri, Carla,Ballestri, Marco,Mulazzani, Quinto G.,Landi, Laura

, p. 4593 - 4601 (2007/10/03)

Thiyl radicals reversibly attack the double bonds of methyl oleate and dioleoyl phosphatidyl choline (DOPC), thus producing methyl elaidate and the corresponding phospholipids containing trans-fatty acid residues in high yield. These processes are radical chain reactions with relatively long chain lengths. The rate constant for the β-elimination of a thiyl radical from the adduct radical has been estimated to be 6 x 106 s-1 at ambient temperature. The cis-trans isomerization of fatty acid residues in DOPC vesicles (multilamellar vesicles and large unilamellar vesicles made by the extrusion technique) by a thiyl radical, generated from biologically relevant thiols, has also been studied in detail. The presence of 0.2 mM oxygen does not influence the effectiveness of cis-trans isomerization in both homogeneous solution and lipid vesicles. This process, which does not cause lipid degradation but permanent modification of the membrane constituents, ultimately influences the barrier properties and functions of biological membranes.

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