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Merck

T4891

甘油三月桂酸酯

≥99%

同義詞:

1,2,3-三(十二烷酰)甘油, 1,2,3-三月桂酰甘油, 三月桂精, 三月桂酸甘油酯, 十三烷菌素, 甘油月桂酸酯

登入 檢視組織與合約價格。

選擇尺寸

暫時無法取得訂價和供貨情況

關於此項目

線性公式:
[CH3(CH2)10COOCH2]2CHOCO(CH2)10CH3
CAS 編號:
分子量::
639.00
UNSPSC Code:
12352211
NACRES:
NA.25
PubChem Substance ID:
EC Number:
208-687-0
Beilstein/REAXYS Number:
1730452
MDL number:

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產品名稱

甘油三月桂酸酯, ≥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

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1 of 4

本產品
T7517T5534T9126
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.:以甘油三月桂酸酯为组分之一,开发药物递送的脂质纳米颗粒。改进的纳米粒子可增强化疗药物紫杉醇的递送和疗效(Dong et al., 2009)。

存儲類別/等級

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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分析證明 (COA)

Lot/Batch Number

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存取文件庫

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
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
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
S Bresson et al.
Chemistry and physics of lipids, 134(2), 119-129 (2005-03-24)
A study of the vibrational behavior of five saturated monoacid triacylglycerides is performed by Raman spectroscopy at room temperature in the 3100-500 cm(-1) spectral range. The splitting of the CO stretching mode leads to conclude on the existence of two
John W Goodrum et al.
Bioresource technology, 84(1), 75-80 (2002-07-26)
In developing compositional models for biomass-based diesel fuel extenders, volatility properties of medium- and long-chain saturated triglycerides are essential to predict the impact of low levels of these compounds in mixtures with short-chain triglycerides. A thermogravimetric analysis (TGA) method for

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