Detail of > 109-59-1
- MSDS Download

- CAS Number:
- 109-59-1
- Name:
Ethanol,2-(1-methylethoxy)-
- Superlist Name:
- 2-Isopropoxyethanol
- Formula:
- C5H12 O2
- Molecular Structure:

- Synonyms:
- Ethanol,2-isopropoxy- (6CI,7CI,8CI); 2-Isopropoxyethanol; 2-Isopropyloxyethanol;2-[(1-Methylethyl)oxy]ethanol; Dowanal EiPAT; Ethylene glycol isopropyl ether;Ethylene glycol monisopropyl ether; Ethylene glycol monoisopropyl ether;Isopropyl Cellosolve; Isopropyl Oxitol; NSC 1259; Ucar AC; b-Hydroxyethyl isopropyl ether
- Molecular Weight:
- 104.17
- EINECS:
- 203-685-6
- Density:
- 0.903
- Melting Point:
- -60 °C
- Boiling Point:
- 131.8 °C at 760 mmHg
- Flash Point:
- 43 ºC
- Solubility:
- Stability Stable. Incompatible with strong oxidizing agents. Combustible. Toxicology Harmful if inhaled or absorbed through the skin.Eye irritant. Typical OEL 22 mg/m3. Toxicity
- Appearance:
- clear colorless liquid
- Hazard Symbols:

- Risk Codes:
- R20/21;R36
- Safety:
- Moderately toxic by skin contact and intraperitoneal routes. Mildly toxic by inhalation and ingestion. A skin and eye irritant. When heated to decomposition it emits acrid smoke and fumes. See also GLYCOL ETHERS.Details
- Transport Information:
- UN 2929
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Reference
- Controlling fines migrations
- Controlling fines migrations. Watkins, Larry A.; Graham, John W.; Salathiel, William M. (Exxon Production Research Co., USA). U.S. US 4018285 19 Apr 1977, 8 pp. (English). (United States of America). CODEN: USXXAM. CLASS: IC: E21B033-138. NCL: 166295000. APPLICATION: US 76-668557 19 Mar 1976. DOCUMENT TYPE: Patent CA Section: 51 (Fossil Fuels, Derivatives, and Related Products) Section cross-reference(s): 37 To decrease migration of fines toward oil and natural gas wells, formations surrounding them are treated with a phenolic resin, which forms a film preventing the fines movement when petroleum or gas is produced from the formation. Thus, a steel core holder packed with sand and satd. with brine was treated sequentially by (1) a solvent preflush with 2-isopropoxyethanol (UCAR Solvent AC) [109-59-1], (2) an injection of a soln. contg. 20 wt.% of a powd. PhOH-HCHO resin (BRPE 4035) [9003-35-4] in MeOH and a silane coupling agent to provide a bond between sand and resin, (3) an overflush with refined paraffinic white oil, and (4) an extn. with brine. Fines migration was effectively controlled without affecting the core permeability.
- Inhibition of metabolic cooperation between Chinese hamster V-79 cells by structurally diverse teratogens
- Inhibition of metabolic cooperation between Chinese hamster V-79 cells by structurally diverse teratogens. Welsch, Frank; Stedman, Donald B. (Dep. Cell Biol., Chem. Ind. Inst. Toxicol., Research Triangle Park, NC 27709, USA). Teratog., Carcinog., Mutagen., 4(3), 285-301 (English) 1984. CODEN: TCMUD8. ISSN: 0270-3211. DOCUMENT TYPE: Journal CA Section: 4 (Toxicology) Chinese hamster cells (V-79) which display a specific form of cell-cell communication called metabolic cooperation were cultured in the presence of structurally diverse chem. teratogens. Among them were TPA (I) [16561-29-8], diphenylhydantoin (DPH) [57-41-0], warfarin [81-81-2], and a series of monoalkyl ethers of ethyleneglycol with alc. chain lengths from Me to Bu. Saccharin and ascorbic acid were examd. to represent 2 chems. which have been tested for teratogenic effects in lab. animals and cause no birth defects. Recovery of 100 6-thioguanine resistant V-79 (6-TGr) cells in coculture with 400,000 6-thioguanine-sensitive V-79 (6-TGs) cells in the presence of 6-thioguanine (6-TG) and the chem. agent was measured. In amts. that neither interfered with colony-forming ability nor caused cytostasis when 100 6-TGr cells were plated alone, all of the substances except for saccharin and vitamin C increased the no. of surviving 6-TGr cells in a concn.-related manner. The recovery was increased by the presence of I (to 100% by 4 ng/mL), DPH (from 26% at 91 mM to 43% at 274 mM), warfarin (from 15.5% at 162 mM to 44.5% at 487 mM), and to variable extents by all 5 glycol ethers. The most efficacious in the latter group of compds. was the isopropyl ether [109-59-1] which raised 6-TGr recovery from 8% at 0.017M to 66% at 0.087M. The teratogens employed inhibited metabolic cooperation. These observations suggest that V-79 cells may be suitable to study inhibition of cell-cell communication as a mechanism of teratogenesis.
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