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Merck

525073

Sigma-Aldrich

Triacetin

greener alternative

99%

Sinónimos:

1,2,3-Triacetoxypropane, 1,2,3-Triacetylglycerol, Glyceryl triacetate

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About This Item

Fórmula lineal:
(CH3COOCH2)2CHOCOCH3
Número de CAS:
Peso molecular:
218.20
Beilstein/REAXYS Number:
1792353
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

7.52 (vs air)

assay

99%

autoignition temp.

809 °F

expl. lim.

1.05 %, 189 °F
7.73 %, 215 °F

greener alternative product characteristics

Less Hazardous Chemical Syntheses
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

refractive index

n25/D 1.429-1.431 (lit.)

bp

258 °C (lit.)

mp

3 °C (lit.)

density

1.16 g/mL at 25 °C (lit.)

greener alternative category

SMILES string

CC(=O)OCC(COC(C)=O)OC(C)=O

InChI

1S/C9H14O6/c1-6(10)13-4-9(15-8(3)12)5-14-7(2)11/h9H,4-5H2,1-3H3

InChI key

URAYPUMNDPQOKB-UHFFFAOYSA-N

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General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Green Chemistry. This product can replace highly toxic diluents in membrane preparation and thus aligns with "Less Hazardous Chemical Syntheses". Click here for more information.

Application

Triacetin can be used as:
  • An additive in the preparation of flax fiber-polylactic acid (PLA) composites due to its compatibility with the polymer and ability to increase the elongation of the plastic.
  • A reactant in the transesterification reaction with methanol using various catalysts.

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

298.4 °F - closed cup

flash_point_c

148 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Los clientes también vieron

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1 of 2

Natural fibres as reinforcement in polylactic acid (PLA) composites
Oksman K, et al.
Composites Science and Technology, 63(9), 1317-1324 (2003)
Transesterification of triacetin with methanol on solid acid and base catalysts
Lopez DE, et al.
Applied Catalysis A: General, 295(2), 97-105 (2005)
Transesterification of triacetin with methanol on Nafion
Lopez DE, et al.
J. Catal., 245(2), 381-391 (2007)
G Sharma et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 76(2), 159-169 (2010-07-27)
Insulin loaded microemulsions were developed adopting a low shear reverse micellar approach using didoceyldimethylammonium bromide (DMAB) as the surfactant, propylene glycol (PG) as the co-surfactant, triacetin (TA) as the oil phase and insulin solution as the aqueous phase. A ternary
C N Madhavarao et al.
Journal of inherited metabolic disease, 32(5), 640-640 (2009-08-18)
Canavan disease (CD) is a fatal dysmyelinating genetic disorder associated with aspartoacylase deficiency, resulting in decreased brain acetate levels and reduced myelin lipid synthesis in the developing brain. Here we tested tolerability of a potent acetate precursor, glyceryl triacetate (GTA)

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