Product No. T59803 (Triethylene glycol dimethyl ether, ReagentPlus®, 99%) does not contain any antioxidants or inhibitors. It consists of neat triethylene glycol dimethyl ether with a specified GC purity ≥ 98.5 %. The actual lot-specific purity often is higher than this value, but the residual impurities in this product are not identified.
T59803
Triethylene glycol dimethyl ether
ReagentPlus®, 99%
Synonym(s):
1,2-Bis(2-methoxyethoxy)ethane, Dimethyltriglycol, NSC 66400, Triglyme
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About This Item
Linear Formula:
CH3O(CH2CH2O)3CH3
CAS Number:
Molecular Weight:
178.23
Beilstein:
1700630
EC Number:
MDL number:
UNSPSC Code:
12352112
PubChem Substance ID:
NACRES:
NA.21
Assay:
99%
bp:
216 °C (lit.)
Pricing and availability is not currently available.
Recommended Products
vapor density
>4.7 (vs air)
Quality Level
product line
ReagentPlus®
Assay
99%
form
liquid
autoignition temp.
375 °F
expl. lim.
8 %
refractive index
n20/D 1.423 (lit.)
bp
216 °C (lit.)
mp
−45 °C (lit.)
density
0.986 g/mL at 25 °C (lit.)
SMILES string
COCCOCCOCCOC
InChI
1S/C8H18O4/c1-9-3-5-11-7-8-12-6-4-10-2/h3-8H2,1-2H3
InChI key
YFNKIDBQEZZDLK-UHFFFAOYSA-N
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General description
Triethyleneglycol dimethyl ether, also known as triglyme, is a member of the glycol ether family and is commonly used as a solvent in industries like electronics, pharmaceuticals, coatings, and more. Triglymes are chemically inert because they lack reactive functional groups, making them well-suited for chemical synthesis. They have strong solvating abilities and demonstrate excellent thermal and chemical stability, which makes them highly valuable as solvents and processing aids in the manufacturing and formulation of industrial chemicals.
Application
Triethylene glycol dimethyl ether can be used as a:
- Extracting solvent in a modified SA-HPSW (Supercritical Anti-Solvent with High-Pressure Solvent Wash) system.
- Solvent in the synthesis of passivated iron nanoparticles.[1]
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Repr. 1B
Supplementary Hazards
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 1
Flash Point(F)
235.4 °F - closed cup
Flash Point(C)
113 °C - closed cup
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Characterization of tetraethylene glycol passivated iron nanoparticles
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This work reports two new silver metalorganic precursors for the chemical vapor deposition of Ag metallic coatings. Both precursors are based on β-diketonate adducts, namely, Ag(hfac)(L) (H-hfac = 1,1,1,5,5,5-hexafluoro-2,4-pentanedione), where L is 1,10-phenanthroline (phen) or 2,5,8,11-tetraoxadodecane (triglyme). Using these ligands
Reproductive toxicology. Triethylene glycol dimethyl ether.
Environmental health perspectives, 105 Suppl 1, 239-240 (1997-02-01)
J D George et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 9(1), 173-181 (1987-07-01)
Triethylene glycol dimethyl ether (triEGdiME) is structurally related to several compounds which produce reproductive and developmental toxicity, including teratogenicity in laboratory animals. In the present study, triEGdiME (0, 250, 500, or 1000 mg/kg/day) was administered by gavage to timed-pregnant CD-1
N L Bossert et al.
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Triethylene glycol and two of its derivatives were evaluated for reproductive toxicity in a continuous breeding protocol with Swiss CD-1 mice. Triethylene glycol (TEG: 0, 0.3, 1.5, and 3%), triethylene glycol diacetate (TGD: 0, 0.75, 1.5, and 3%), and triethylene
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