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D9758

Sigma-Aldrich

Dilaurin Mixed Isomers

≥99%

Sinônimo(s):

Dilaurin Isomer Mixture

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About This Item

Fórmula empírica (Notação de Hill):
C27H52O5
Número CAS:
27638-00-2
Peso molecular:
456.70
Número CE:
248-586-9
Código UNSPSC:
12352211
ID de substância PubChem:
329798911
NACRES:
NA.25

fonte biológica

plant kernels (palm)

Ensaio

≥99%

forma

powder

grupo funcional

ester

tipo de lipídio

neutral glycerides

Condições de expedição

ambient

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

CCCCCCCCCCCC(=O)OCC(O)COC(=O)CCCCCCCCCCC.CCCCCCCCCCCC(=O)OCC(CO)OC(=O)CCCCCCCCCCC

InChI

1S/2C27H52O5/c1-3-5-7-9-11-13-15-17-19-21-26(29)31-23-25(28)24-32-27(30)22-20-18-16-14-12-10-8-6-4-2;1-3-5-7-9-11-13-15-17-19-21-26(29)31-24-25(23-28)32-27(30)22-20-18-16-14-12-10-8-6-4-2/h2*25,28H,3-24H2,1-2H3

chave InChI

RURSPNRVQHSFCU-UHFFFAOYSA-N

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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1,2-Dioleoyl-rac-glycerol ≥97%

Sigma-Aldrich

D8394

1,2-Dioleoyl-rac-glycerol

1-Stearoyl-rac-glycerol ≥99%

Sigma-Aldrich

M2015

1-Stearoyl-rac-glycerol

1-Decanoyl-rac-glycerol ≥99%

Sigma-Aldrich

M2140

1-Decanoyl-rac-glycerol

1,2-Dioleoyl-sn-glycerol ≥97%

Sigma-Aldrich

D0138

1,2-Dioleoyl-sn-glycerol

Supelco

Supelco

1787-1AMP

Lipid Standard, Mono-, Di-, & Triglyceride Mix

Dioleoylglycerol ≥99%, mixture of 1,3- and 1,2-isomers, liquid

Sigma-Aldrich

D8894

Dioleoylglycerol

Glyceryl trioctanoate ≥95% (GC)

Sigma-Aldrich

T9126

Glyceryl trioctanoate

C M Mansbach et al.
The Journal of clinical investigation, 69(2), 368-376 (1982-02-01)
We evaluated phospholipase activity in the intestine of rats and other species. Phospholipase activity was assayed by a surface barostat technique or an egg yolk titration system. Mucosal activity was found only by the surface barostat technique with phosphatidylglycerol as
D Lairon et al.
Biochimica et biophysica acta, 618(1), 106-118 (1980-04-18)
We report a new technique which allows us to follow the lipolysis of monomolecular films in the presence of bile salts by using a 'zero-order' trough (Verger, R. and de Haas, G.H. (1973) Chem. Phys. Lipids 10, 127). The effects
Glycerol conformation and molecular packing of membrane lipids. The crystal structure of 2,3-dilauroyl-D-glycerol.
I Pascher et al.
Journal of molecular biology, 153(3), 791-806 (1981-12-15)
G Vanderkooi
Chemistry and physics of lipids, 55(3), 253-264 (1990-09-01)
Computational procedures have been developed by which the total energy of a lipid multibilayer can be calculated and minimized. The energy is expressed as a sum of non-bonded, electrostatic, hydrogen bonded and torsional energy terms and includes intramolecular and intermolecular
J A Hamilton et al.
The Journal of biological chemistry, 266(2), 1177-1186 (1991-01-15)
The interaction of diacylglycerols, primarily 1,2-dilauroyl-sn-glycerol (1,2-DLG), with egg phosphatidylcholine (PC) bilayers was studied by NMR spectroscopy and other physical techniques. In the low proportions used (less than or equal to 20 mol % with respect to total lipid), 1,2-DLG

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