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07-2980

Sigma-Aldrich

Diethylene glycol monoethyl ether

SAJ first grade, ≥98.0%

Sinônimo(s):

2-(2-Ethoxyethoxy)ethanol, CARBITOL™, Diethylene glycol ethyl ether, Ethyldiglycol

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About This Item

Fórmula linear:
C2H5OCH2CH2OCH2CH2OH
Número CAS:
111-90-0
Peso molecular:
134.17
Beilstein:
1736441
Número CE:
203-919-7
Número MDL:
MFCD00002872
Código UNSPSC:
12352112
ID de substância PubChem:
329748401

grau

SAJ first grade

densidade de vapor

4.63 (vs air)

pressão de vapor

0.12 mmHg ( 20 °C)

Ensaio

≥98.0%

forma

liquid

Lim. expl.

1.2 %, 135 °F
23.5 %, 182 °F

disponibilidade

available only in Japan

índice de refração

n20/D 1.427 (lit.)

pb

202 °C (lit.)

densidade

0.999 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

CCOCCOCCO

InChI

1S/C6H14O3/c1-2-8-5-6-9-4-3-7/h7H,2-6H2,1H3

chave InChI

XXJWXESWEXIICW-UHFFFAOYSA-N

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Informações legais

CARBITOL is a trademark of The Dow Chemical Company or an affiliated company of Dow

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

204.8 °F - closed cup

Ponto de fulgor (°C)

96 °C - closed cup

Equipamento de proteção individual

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

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Yousef Javadzadeh et al.
Colloids and surfaces. B, Biointerfaces, 82(2), 422-426 (2010-10-19)
Regarding the potential severe toxicity associated with systemic administration of methotrexate (MTX), a topical formulation might be of greater utility for the treatment of psoriasis and other hyperproliferative skin disorders. One of the presumed reasons for the lack of clinical
Liandong Hu et al.
International journal of pharmaceutics, 420(2), 251-255 (2011-09-13)
The objective of the present study was to formulate a microemulsion system for oral administration to improve the solubility and bioavailability of fenofibrate. Various formulations were prepared using different ratios of oils, surfactants and co-surfactants (S&CoS). Pseudo-ternary phase diagrams were
Dong Hoon Oh et al.
International journal of pharmaceutics, 420(2), 412-418 (2011-09-29)
In order to compare the effects of hydrophilic and hydrophobic solid carrier on the formation of solid self-microemulsifying drug delivery system (SMEDDS), two solid SMEDDS formulations were prepared by spray-drying the solutions containing liquid SMEDDS and solid carriers. Colloidal silica
Hyun-Jong Cho et al.
International journal of pharmaceutics, 423(2), 153-160 (2012-01-03)
To achieve rapid onset of action and improved bioavailability of udenafil, a microemulsion system was developed for its intranasal delivery. Phase behavior, particle size, transmission electron microscope (TEM) images, and the drug solubilization capacity of the microemulsion were investigated. A
Roberta Censi et al.
Drug development and industrial pharmacy, 38(9), 1128-1133 (2011-12-23)
A microemulsion for the cutaneous release of quercetin was prepared. An aqueous phase, containing 40% Transcutol® P as solubilizing agent and permeation enhancer, was emulsified with Labrafil® as oil phase and Labrasol®/Capryol™ 90 as Solvent/Co-solvent. Quercetin was dissolved in the
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