Home Other Building Blocks 9-Octadecenoic acid (9Z)-, 1,1'-(2-hydroxy-1,3-propanediyl) ester

9-Octadecenoic acid (9Z)-, 1,1'-(2-hydroxy-1,3-propanediyl) ester

CAS No.:
2465-32-9
Catalog Number:
AG002OY4
Molecular Formula:
Molecular Weight:
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Product Description
Catalog Number:
AG002OY4
Chemical Name:
9-Octadecenoic acid (9Z)-, 1,1'-(2-hydroxy-1,3-propanediyl) ester
CAS Number:
2465-32-9
MDL Number:
MFCD00042913
IUPAC Name:
[2-hydroxy-3-[(Z)-octadec-9-enoyl]oxypropyl] (Z)-octadec-9-enoate
InChI:
InChI=1S/C39H72O5/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-38(41)43-35-37(40)36-44-39(42)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h17-20,37,40H,3-16,21-36H2,1-2H3/b19-17-,20-18-
InChI Key:
DRAWQKGUORNASA-CLFAGFIQSA-N
EC Number:
219-569-3
UNII:
ERF7S0XX7K
Properties
Complexity:
615  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
2  
Exact Mass:
620.538g/mol
Formal Charge:
0
Heavy Atom Count:
44  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
621g/mol
Monoisotopic Mass:
620.538g/mol
Rotatable Bond Count:
36  
Topological Polar Surface Area:
72.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
14.3  
Literature
Title Journal
Rational synthesis of 1,3-diolein by enzymatic esterification. Journal of biotechnology 20120531
The mechanism of solvent effect on the positional selectivity of Candida antarctica lipase B during 1,3-diolein synthesis by esterification. Bioresource technology 20111201
The solvent influence on the positional selectivity of Novozym 435 during 1,3-diolein synthesis by esterification. Bioresource technology 20100401
Fat mobilization in adipose tissue is promoted by adipose triglyceride lipase. Science (New York, N.Y.) 20041119
Properties