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93171

Sigma-Aldrich

Diethylene glycol

BioUltra, ≥99.0% (GC)

Sinónimos:

2,2′-Oxydiethanol, 2-Hydroxyethyl ether, Bis(2-hydroxyethyl) ether, Diglycol

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About This Item

Fórmula lineal:
(HOCH2CH2)2O
Número de CAS:
111-46-6
Peso molecular:
106.12
Beilstein/REAXYS Number:
969209
EC Number:
203-872-2
MDL number:
MFCD00002882
UNSPSC Code:
12352137
PubChem Substance ID:
57653523
NACRES:
NA.25

vapor density

2.14 (vs air)

Quality Level

200

vapor pressure

0.01 mmHg ( 20 °C)

description

non-ionic

product line

BioUltra

assay

≥99.0% (GC)

form

liquid
viscous liquid

autoignition temp.

442 °F

expl. lim.

2-12.3 %

impurities

insoluble matter, passes filter test
≤30 mg/kg peroxides (as H2O2)

refractive index

n20/D 1.447 (lit.)
n20/D 1.447

pH

5.5-7.0 (25 °C, 50 mg/mL in H2O)

bp

245 °C (lit.)

mp

−10 °C (lit.)

solubility

H2O: 50 mg/mL at 20 °C, clear, colorless

density

1.118 g/mL at 25 °C (lit.)

anion traces

chloride (Cl-): ≤50 mg/kg
sulfate (SO42-): ≤50 mg/kg

cation traces

Al: ≤10 mg/kg
As: ≤0.1 mg/kg
Ba: ≤5 mg/kg
Bi: ≤5 mg/kg
Ca: ≤10 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
K: ≤200 mg/kg
Li: ≤5 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Mo: ≤5 mg/kg
Na: ≤200 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Sr: ≤5 mg/kg
Zn: ≤5 mg/kg

SMILES string

OCCOCCO

λ

50 mg/mL in H2O

UV absorption

λ: 260 nm Amax: ≤0.060
λ: 280 nm Amax: ≤0.030

InChI

1S/C4H10O3/c5-1-3-7-4-2-6/h5-6H,1-4H2

InChI key

MTHSVFCYNBDYFN-UHFFFAOYSA-N

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Application

Diethylene glycol (diglycol) is used in biomaterials engineering to functionalize peptide nanofibers to improve their aggregation and proteolytic degradation properties. Diethylene glycol may be used as a solvent, reducing agent and derivatizing agent in the preparation of various types of nanoparticles.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

280.4 °F - closed cup

flash_point_c

138 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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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Xiao-Yan Yan et al.
Chemical communications (Cambridge, England), 48(13), 1892-1894 (2012-01-10)
Cuprous oxide (Cu(2)O) nanoparticles dispersed on reduced graphene oxide (RGO) were prepared by reducing copper acetate supported on graphite oxide using diethylene glycol as both solvent and reducing agent. The Cu(2)O/RGO composite exhibits excellent catalytic activity and remarkable tolerance to
Ze-Jian Wang et al.
Journal of photochemistry and photobiology. B, Biology, 115, 16-24 (2012-07-17)
Photodynamic therapy (PDT) has recently been proposed as a possible indication in the conservative treatment of hereditary retinoblastoma. In order to create photosensitizers with enhanced targeting ability toward retinoblastoma cells, meso-tetraphenylporphyrins bearing one glycodendrimeric moiety have been synthesized. The binding
Parisa Sadatmousavi et al.
Acta biomaterialia, 8(9), 3241-3250 (2012-05-30)
Self-assembling peptide nanofibers have emerged as important nanobiomaterials, with such applications as delivery of therapeutic agents and vaccines, nanofabrication and biomineralization, tissue engineering and regenerative medicine. Recently a new class of self-assembling peptides has been introduced, which takes into consideration
Leo J Schep et al.
Clinical toxicology (Philadelphia, Pa.), 47(6), 525-535 (2009-07-10)
Diethylene glycol (DEG) is a clear, colorless, practically odorless, viscous, hygroscopic liquid with a sweetish taste. In addition to its use in a wide range of industrial products, it has also been involved in a number of prominent mass poisonings
Bichismita Sahu et al.
The Journal of organic chemistry, 76(14), 5614-5627 (2011-05-31)
Developed in the early 1990s, peptide nucleic acid (PNA) has emerged as a promising class of nucleic acid mimic because of its strong binding affinity and sequence selectivity toward DNA and RNA and resistance to enzymatic degradation by proteases and
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