T4891

Glyceryl tridodecanoate

Name: Glyceryl tridodecanoate
Brand: SIGMA
Price: 51867 KRW
Availability: InStock

≥99%

동의어(들):

1,2,3-Tridodecanoylglycerol, 1,2,3-Trilauroylglycerol, Glycerol trilaurate, Glyceryl trilaurate, Tridodecanoin, Trilaurin

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100 MG

₩51,867

5 G

₩307,647

₩51,867

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제품정보 (DICE 배송 시 비용 별도)

Linear Formula:

[CH₃(CH₂)₁₀COOCH₂]₂CHOCO(CH₂)₁₀CH₃

CAS 번호:

538-24-9

Molecular Weight:

639.00

UNSPSC Code:

12352211

NACRES:

NA.25

PubChem Substance ID:

24900235

EC Number:

208-687-0

Beilstein/REAXYS Number:

1730452

MDL number:

MFCD00026559

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도움 문의

제품 이름

Glyceryl tridodecanoate, ≥99%

InChI key

VMPHSYLJUKZBJJ-UHFFFAOYSA-N

InChI

1S/C39H74O6/c1-4-7-10-13-16-19-22-25-28-31-37(40)43-34-36(45-39(42)33-30-27-24-21-18-15-12-9-6-3)35-44-38(41)32-29-26-23-20-17-14-11-8-5-2/h36H,4-35H2,1-3H3

SMILES string

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

biological source

plant

assay

≥99%

form

powder

mp

46.5 °C (lit.)

functional group

ester

lipid type

neutral glycerides

shipped in

ambient

storage temp.

−20°C

Quality Level

200

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차이점 표시

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이 품목	T7517	T5534	T9126
Sigma-Aldrich T4891 Glyceryl tridodecanoate	Sigma-Aldrich T7517 Glyceryl tridecanoate	Sigma-Aldrich T5534 Glyceryl triundecanoate	Sigma-Aldrich T9126 Glyceryl trioctanoate
assay ≥99%	assay ≥99% (GC)	assay ≥98%	assay ≥95% (GC)
functional group ester	functional group ester	functional group ester	functional group ester
biological source plant	biological source -	biological source synthetic	biological source vegetable oil ( (coconut and palm kernel oils))
form powder	form powder	form solid	form liquid
storage temp. −20°C	storage temp. −20°C	storage temp. −20°C	storage temp. 2-8°C
shipped in ambient	shipped in ambient	shipped in ambient	shipped in ambient

Application

Development of new lipid-based paclitaxel nanoparticles using sequential simplex optimization.: This article presents the development of lipid-based nanoparticles for drug delivery, utilizing glyceryl tridodecanoate as a component. The optimized nanoparticles show potential for improved delivery and efficacy of paclitaxel, a chemotherapeutic agent (Dong et al., 2009).

저장 등급

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Determination of positional distribution of butyryl groups in milkfat triacylglycerols, triacylglycerol mixtures, and isolated positional isomers of triacylglycerols by gas chromatography and 1H nuclear magnetic resonance spectroscopy.

P Kalo et al.

Lipids, 31(3), 331-336 (1996-03-01)

Positional isomers (1-butyryl-2X-3Y-rac-glycerol and 2-butyryl-1X-3Y-rac-glycerol; X,Y = long-chain acyls) of saturated triacylglycerols (TAG) within 34 and 40 acyl carbons were shown to separate in two chromatographic peaks on immobilized phenyl(65%)methylsilicone column by gas-liquid chromatography, and on reversed-phase ODS-1 column by

Modeling the solid-liquid phase transition in saturated triglycerides.

David A Pink et al.

The Journal of chemical physics, 132(5), 054502-054502 (2010-02-09)

We investigated theoretically two competing published scenarios for the melting transition of the triglyceride trilaurin (TL): those of (1) Corkery et al. [Langmuir 23, 7241 (2007)], in which the average state of each TL molecule in the liquid phase is

Hydration of an amphiphilic excipient, Gelucire 44/14.

A Svensson et al.

International journal of pharmaceutics, 281(1-2), 107-118 (2004-08-04)

The incorporation of drugs into Gelucires has been reported to increase the dissolution rate of poorly soluble drugs, often leading to improved drug bioavailability. In pharmaceutical applications, it is important to know how the excipient interacts with the drug, and

Synthesis of trilaurin by developing pisa seeds (Actinodaphne hookeri).

A Sreenivas et al.

Archives of biochemistry and biophysics, 311(2), 229-234 (1994-06-01)

The developing seeds of Actinodaphne hookeri were investigated to delineate their ability to synthesize large amounts of trilaurin. Until 88 days after flowering the embryos contained 71% neutral lipids (NL) and 29% phospholipids (PL) and both these components contained C16:0

Pressure-induced phase transitions in triacylglycerides.

Peter Ferstl et al.

Annals of the New York Academy of Sciences, 1189, 62-67 (2010-03-18)

The melting point of triacylglycerides (TAGs) under atmospheric pressure depends on both the fatty acid composition and crystalline structure of the polymorphic state, which are influenced by the temperature treatment history of the TAG. In this contribution, the additional effect

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Glyceryl tridodecanoate