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Key Documents

D1657

Sigma-Aldrich

1,3-Dioleoyl-2-palmitoylglycerol

Sinônimo(s):

1,3-Di(cis-9-octadecenoyl)-2-hexadecanoylglycerol

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About This Item

Fórmula empírica (Notação de Hill):
C55H102O6
Número CAS:
Peso molecular:
859.39
Número MDL:
Código UNSPSC:
12352211
ID de substância PubChem:
NACRES:
NA.25

grupo funcional

ester

Nível de qualidade

tipo de lipídio

neutral glycerides

cadeia de caracteres SMILES

CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC\C=C\CCCCCCCC)COC(=O)CCCCCCC\C=C\CCCCCCCC

InChI

1S/C55H102O6/c1-4-7-10-13-16-19-22-25-27-30-32-35-38-41-44-47-53(56)59-50-52(61-55(58)49-46-43-40-37-34-29-24-21-18-15-12-9-6-3)51-60-54(57)48-45-42-39-36-33-31-28-26-23-20-17-14-11-8-5-2/h25-28,52H,4-24,29-51H2,1-3H3/b27-25+,28-26+

chave InChI

PPTGNVIVNZLPPS-NBHCHVEOSA-N

Descrição geral

1,3-Dioleoyl-2-palmitoylglycerol (OPO) is a structured triglyceride in infant formula. Its structure is like human milk fat (HMF).

Aplicação

1,3-Dioleoyl-2-palmitoylglycerol (OPO) has been used:
  • as a synthetic triacylglycerol (TAG) standard to investigate the fragmentation patterns of TAGs in milk fat by the multi-dimension mass spectrometry (MDMS) method
  • as a lipid standard to analyze OPO content/TAG compositions in the acidolysis products by high-performance liquid chromatography-evaporative light scattering detector (HPLC-ELSD)
  • as a standard in silver-ion HPLC separation of OPO-rich human milk fat substitute (HMFS)

Ações bioquímicas/fisiológicas

1,3-Dioleoyl-2-palmitoylglycerol (OPO) exerts several beneficial effects on infants, including remitting constipation, improved calcium and fatty acid absorption, and improved bone development.

Embalagem

Sealed ampule

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

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)

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Jeung Hee Lee et al.
New biotechnology, 27(1), 38-45 (2009-11-03)
1,3-Dioleoyl-2-palmitoylglycerol (OPO)-rich human milk fat substitute (HMFS) was synthesized from tripalmitin-rich fraction and ethyl oleate by a lipase-catalyzed interesterification. Response surface methodology was employed to optimize its OPO content and acyl migration with reaction factors - substrate mole ratio of
A Rosa et al.
Food & function, 7(9), 4092-4103 (2016-09-08)
We explored the changes in viability and lipid profile occurring in cancer cells, murine melanoma cells (B16F10 cells) and human cervical carcinoma cells (HeLa cells), when exposed to 24 h-treatments with an n-3 PUFA-rich oil obtained by supercritical extraction with
Fei Teng et al.
Food chemistry, 297, 124976-124976 (2019-06-30)
Milk fat is arguably one of the most complex fats found in nature and varies widely between animal species. Analysis of its digestion products is tremendously challenging, due to the complexity, diversity, and large range of concentrations of triacylglycerols (TAGs)

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