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| | Triethylene glycol dimethyl ether Basic information |
| | Triethylene glycol dimethyl ether Chemical Properties |
| Melting point | −45 °C(lit.) | | Boiling point | 216 °C(lit.) | | density | 0.986 g/mL at 25 °C(lit.) | | vapor density | >4.7 (vs air) | | vapor pressure | 1.2 hPa (20 °C) | | refractive index | n20/D 1.423(lit.) | | Fp | 231 °F | | storage temp. | Store below +30°C. | | solubility | >1000g/l soluble | | form | Liquid | | color | APHA: ≤20 | | explosive limit | 0.7%(V) | | Water Solubility | Soluble | | Sensitive | Hygroscopic | | Merck | 14,9692 | | BRN | 1700630 | | Dielectric constant | 7.5 | | InChIKey | YFNKIDBQEZZDLK-UHFFFAOYSA-N | | LogP | -0.52 at 20℃ | | CAS DataBase Reference | 112-49-2(CAS DataBase Reference) | | NIST Chemistry Reference | 2,5,8,11-Tetraoxadodecane(112-49-2) | | EPA Substance Registry System | Triethylene glycol dimethyl ether (112-49-2) |
| Hazard Codes | T | | Risk Statements | 61-19-62 | | Safety Statements | 53-45 | | WGK Germany | 1 | | RTECS | XF0665000 | | F | 3 | | Autoignition Temperature | 375 °F | | TSCA | Yes | | HS Code | 29094990 | | Toxicity | LD50 orally in Rabbit: 5390 mg/kg |
| | Triethylene glycol dimethyl ether Usage And Synthesis |
| Chemical Properties | Water-white liquid; mild ether odor. D
0.9862 (20/20C), refr index 1.4233 (20C), flash p
232F (111C), bp 216.0C (760mmHg), 153.6C (100
mm Hg), fp ?46C. Completely soluble in water
and hydrocarbons at 20C. May contain peroxides.
Combustible. | | Uses | Labelled Triglyme. It is used as a solvent. | | Uses | Triethylene glycol dimethyl ether is used as a solvent for gases and coupling immiscible liquid. It is also used to prepare perfluoro-triethyleneglycoldimethylether. | | Uses | Triethylene glycol dimethyl ether may be used as an analytical standard for the quantification of the analyte in water samples using in vitro bioassays and chemical screening technique. | | Definition | ChEBI: A polyether that consists of dodecane in which the carbon atoms at positions 2, 5, 8 and 11 are replaced by oxygen atoms. | | Application | Triethylene glycol dimethyl ether is a member of the glycol ether class of industrial solvents. These solvents are widely used to manufacture protective coatings such as lacquers, metal coatings, baking enamels, phenolic varnishes, epoxy resin coatings, and alkyl resins[1].
| | Reactivity Profile | TRIETHYLENE GLYCOL DIMETHYL ETHER forms explosive peroxides on prolonged exposure to air. Its decomposition products may be sensitive to shock. The bulk chemical is stable for 2 weeks at temperatures up to 140° F when protected from light. TRIETHYLENE GLYCOL DIMETHYL ETHER is incompatible with strong oxidizers. TRIETHYLENE GLYCOL DIMETHYL ETHER is also incompatible with strong acids. TRIETHYLENE GLYCOL DIMETHYL ETHER may react with peroxides, oxygen, nitric acid and sulfuric acid. . | | Flammability and Explosibility | Non flammable | | Toxicology |
Triethylene glycol dimethyl ether (triEGdiME) is a widely used organic solvent. It is structurally related to several compounds that produce reproductive and developmental toxicity, including teratogenicity in laboratory animals. In the present studies, triEGdiME (0, 75, 125, 175, or 250 mg/kg/day) is administered by gavage in distilled water to timed-pregnant New Zealand white rabbits (15-25 dams/group) during major organogenesis [Gestational Days (gd) 6-19]. In the triEGdiME study, clinical signs of toxicity were minimal, and there was no increased maternal mortality. Maternal body weight and gravid uterine weight were significantly reduced at 250 mg/kg/day, whereas maternal weight gain during treatment was significant. They were depressed at doses of 175 mg/kg/day and above. Prenatal mortality was significantly increased at 250 mg triEGdiME/kg/day. TriEGdiME at doses of 175 and 250 mg/kg/day caused a significant increase in the incidence of malformed fetuses per litter. Malformations noted most frequently in fetuses of normal size included anonychia (missing toenails with no digital abnormalities), abnormally small spleen, and hydronephrosis[1].
| | Purification Methods | Reflux it with, and distil it from sodium hydride or LiAlH4. [Beilstein 1 IV 2401.] |
| | Triethylene glycol dimethyl ether Preparation Products And Raw materials |
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