| Identification | More | [Name]
2-Methoxyethanol | [CAS]
109-86-4 | [Synonyms]
2-METHOXYETHANOL
ACIDIFIED CLEAR WATER
AMYL ALCOHOL
APPLICLEAR-WATER
AQUALINE COMPLETE
AQUALINE COMPLETE 1
AQUALINE COMPLETE 2
AQUALINE COMPLETE 5
AQUALINE COMPLETE 5K
AQUALINE ELECTROLYTE A
AQUALINE ELECTROLYTE AG
AQUALINE ELECTROLYTE C
AQUALINE ELECTROLYTE CG
AQUALINE MATRIX K
AQUALINE(R) COMPLETE 1
AQUALINE(R) COMPLETE 2
AQUALINE(R) COMPLETE 5
AQUALINE(R) COMPLETE 5K
AQUALINE(R) ELECTROLYTE A
AQUALINE(R) ELECTROLYTE AD | [EINECS(EC#)]
231-791-2 | [Molecular Formula]
C3H8O2 | [MDL Number]
MFCD00081734 | [Molecular Weight]
76.09 | [MOL File]
109-86-4.mol |
| Chemical Properties | Back Directory | [Appearance]
Ethylene glycol monomethyl ether is a colorless liquid with a slight ethereal odor. The Odor Threshold
is 0.92.3 ppm. | [Melting point ]
-85 °C | [Boiling point ]
124-125 °C(lit.) | [density ]
0.965 g/mL at 25 °C(lit.) | [vapor density ]
2.62 (vs air)
| [vapor pressure ]
6.17 mm Hg ( 20 °C)
| [refractive index ]
n20/D 1.402(lit.)
| [Fp ]
115 °F
| [storage temp. ]
5°C | [solubility ]
Very soluble in acetone, dimethylsulfoxide, and 95% ethanol (quoted, Keith and Walters, 1992).
Miscible with N,N-dimethylformamide, ether, and glycerol (Windholz et al., 1983). | [form ]
Liquid | [pka]
15.7(at 25℃) | [color ]
green cap
| [Odor]
Mild ethereal. | [PH Range]
5- 7 at 25 °C | [Relative polarity]
1 | [Stability:]
Stable, but contact with air may lead to the formation of explosive peroxides. A peroxide test should be carried out before this material is used if it has been exposed to air for some time, especially if it is to be purified by distillation. Contact with strong oxidizing agents may cause fire or explosion. Incompatible with strong bases, ac | [explosive limit]
2.5-20%(V) | [Water Solubility ]
SOLUBLE | [λmax]
λ: 213 nm Amax: 1.00
λ: 240 nm Amax: 0.20
λ: 260 nm Amax: 0.05
λ: 300-400 nm Amax: 0.01 | [Merck ]
14,6038 | [BRN ]
1731074 | [Henry's Law Constant]
(x 10-2 atm?m3/mol):
4.41, 3.63, 11.6, 3.09, and 3.813 at 10, 15, 20, 25, and 30 °C, respectively (EPICS, Ashworth et
al., 1988) | [Exposure limits]
TLV-TWA skin 5 ppm (15.5 mg/m3)
(ACGIH), 25 ppm (77.5 mg/m3) (OSHA). | [InChIKey]
XNWFRZJHXBZDAG-UHFFFAOYSA-N | [Uses]
ethylene glycol monomethyl ether (ethoxyethanol) is considered a non-comedogenic raw material. It is used as a solvent in nail products and as a stabilizer in cosmetic emulsions. It is able to penetrate the skin and may cause skin irritation. | [CAS DataBase Reference]
109-86-4(CAS DataBase Reference) | [NIST Chemistry Reference]
Ethanol, 2-methoxy-(109-86-4) | [EPA Substance Registry System]
109-86-4(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
T,F,C | [Risk Statements ]
R60:May impair fertility.
R61:May cause harm to the unborn child.
R10:Flammable.
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R39/23/24/25:Toxic: danger of very serious irreversible effects through inhalation, in contact with skin and if swallowed .
R23/24/25:Toxic by inhalation, in contact with skin and if swallowed .
R11:Highly Flammable.
R35:Causes severe burns. | [Safety Statements ]
S53:Avoid exposure-obtain special instruction before use .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S36/37:Wear suitable protective clothing and gloves .
S16:Keep away from sources of ignition-No smoking .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) . | [RIDADR ]
UN 1188 3/PG 3
| [WGK Germany ]
3
| [RTECS ]
ZC0110000
| [F ]
10 | [Autoignition Temperature]
548 °F | [TSCA ]
Yes | [HazardClass ]
3 | [PackingGroup ]
III | [HS Code ]
29094900 | [Safety Profile]
: Moderately toxic to
humans by ingestion. Moderately toxic experimentally by ingestion, inhalation, shin
contact, intraperitoneal, and intravenous
routes. Human systemic effects by
inhalation: change in motor activity,
tremors, and convulsions. Experimental
teratogenic and reproductive effects. A skin
and eye irritant. Mutation data reported.
When used under conditions that do not
require the application of heat, thts material
probably presents little hazard to health.
However, in the manufacture of fused
collars which require pressing with a hot
iron, cases have been reported showing
disturbance of the hemopoietic system with
or without neurologcal signs and
symptoms. The blood picture may resemble
that produced by exposure to benzene. Two
cases reported had severe aplastic anemia
with tremors and marked mental dullness.
The persons affected had been exposed to
vapors of methyl "Cellosolve," ethanol,
methanol, ethyl acetate, and petroleum
naphtha.
flame. A moderate explosion hazard. Can
react with oxidizing materials to form
explosive peroxides. To fight fire, use
alcohol foam, CO2, dry chemical. When
heated to decomposition it emits acrid
smoke and irritating fumes. See also
GLYCOL ETHERS.
Flammable liquid when exposed to heat or | [Hazardous Substances Data]
109-86-4(Hazardous Substances Data) | [Toxicity]
LD50 in rats, guinea pigs (mg/kg): 2460, 950 orally (Smyth); LC50 (7 hr in air) in mice: 4.6 mg/l (Werner) | [IDLA]
200 ppm |
| Hazard Information | Back Directory | [General Description]
A clear colorless liquid. Flash point of 110°F. Less dense than water. Vapors are heavier than air. | [Reactivity Profile]
ETHYLENE GLYCOL MONOMETHYL ETHER(109-86-4) is incompatible with oxygen and strong oxidizing agents. Contact with bases may result in decomposition. Incompatible with acid chlorides and acid anhydrides. . ETHYLENE GLYCOL MONOMETHYL ETHER(109-86-4) forms explosive peroxides. | [Air & Water Reactions]
Flammable. Water soluble. | [Hazard]
Toxic by ingestion and inhalation. Moderate fire risk. Toxic by skin absorption. Questionable
carcinogen. | [Health Hazard]
Irritation of skin and eyes. Chronic exposure may also cause weakness, sleepiness, headache, gastrointestinal upset, weight loss, change of personality. | [Potential Exposure]
Ethylene glycol monomethyl ether is
used as a jet fuel additive; solvent for protective coating;
and in chemical synthesis. Ethylene glycol ethers are used
as solvents for resins used in the electronics industry, lacquers, paints, varnishes, gum, perfume; dyes and inks; and
as a constituent of painting pastes, cleaning compounds;
liquid soaps; cosmetics, nitrocellulose, and hydraulic fluids | [Fire Hazard]
HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water. | [First aid]
If this chemical gets into the eyes, remove any
contact lenses at once and irrigate immediately for at least
15 minutes, occasionally lifting upper and lower lids. Seek
medical attention immediately. If this chemical contacts the
skin, remove contaminated clothing and wash immediately
with soap and water. Seek medical attention immediately.
If this chemical has been inhaled, remove from exposure,
begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR if
heart action has stopped. Transfer promptly to a medical
facility. When this chemical has been swallowed, get medical attention. Give large quantities of water and induce
vomiting. Do not make an unconscious person vomit.
Medical observation is recommended for 24 to 48 hours
after breathing overexposure, as pulmonary edema may be
delayed. As first aid for pulmonary edema, a doctor or
authorized paramedic may consider administering a drug or
other inhalation therapy | [Shipping]
UN1188 Ethylene glycol monomethyl ether,
Hazard Class: 3; Labels: 3-Flammable liquid | [Incompatibilities]
Vapors may form explosive mixture
with air. Heat or oxidizers may cause the formation of
unstable peroxides. Attacks many metals. Strong oxidizers
may cause fire and explosions. Strong bases cause decomposition and the formation of toxic gas. Attacks some plastics, rubber and coatings. May accumulate static electrical
charges, and may cause ignition of its vapors. | [Description]
Methoxyethanol is a glycol ether that has been known since the
1920s, but its use significantly increased in the 1970s. Cellosolve
was a solvent product containing glycol ethers and
registered in the 1920s by Carbide and Carbon Chemicals
Corp. Glycol ethers are derived from either ethylene oxide
(E-series) or propylene oxide (p-series) combined with an
alcohol. Methoxyethanol is an E-series glycol ether derived
from methanol and ethylene oxide. Other commonly used
glycol ethers include ethoxyethanol, butoxyethanol, and
methoxypropanol. Use of methoxyethanol has declined in
recent years due to risk management procedures and replacement
by other substances. | [Chemical Properties]
2-Methoxyethanol is a colorless liquid with a slight ethereal odor. The Odor Threshold is 0.92.3 ppm. It is miscible with water and with aliphatic and aromatic hydrocarbons. It is a solvent for essential oils, lignin, dammar, Elemi Essential Oil, ester gum, kauri, mastic, rosin, sandarac resin, shellac, Zanzibar, nitrocellulose, cellulose acetate, alcohol-soluble dyes and many synthetic resins. Its solvency far cellulose esters is augmented when a ketone or a halogenated hydrocarbon i s added. The uses for 2-Methoxyethanol are as a solvent in quick-drying varnishes and enamels, in conjunction with aliphatic, aromatic and halogenated hydrocarbons, alcohols and ketones; in solvent mixtures and thinners for lacquers and dopes; in the manufacture of synthetic resin plasticizers and as a penetrating and leveling agent in dyeing processes, especially in the dyeing of leather, animal and vegetable fibers. Other uses are as o fixative in perfumes and as a solvent in odorless nail-polish lacquers. 2-Methoxyethanol should not be added to nitrocellulose lacquers containing coumarone resins or ester gum because it will cause incompatibility between these substances. | [Waste Disposal]
Concentrated waste containing no peroxides: discharge liquid at a controlled rate near
a pilot flame. Concentrated waste containing peroxides:
perforation of a container of the waste from a safe distance
followed by open burning. | [Physical properties]
Colorless liquid with a mild, ether-like odor. Experimentally determined detection and recognition
odor threshold concentrations were <300 μg/m3 (<96 ppbv) and 700 μg/m3 (220 ppbv), respectively
(Hellman and Small, 1974). | [Definition]
ChEBI: A hydroxyether that is ethanol substituted by a methoxy group at position 2. | [Flammability and Explosibility]
Flammable | [Chemical Reactivity]
Reactivity with Water No reaction; Reactivity with Common Materials: No reaction; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent. | [Carcinogenicity]
There are no experimental carcinogenicity
or cancer epidemiology data relating to this
chemical , but some short-term test data are available
and are summarized in the section on genetic and related
cellular effects. | [Environmental Fate]
Photolytic. Grosjean (1997) reported an atmospheric rate constant of 1.25 x 10-11
cm3/molecule?sec at 298 K for the reaction of methyl cellosolve and OH radicals. Based on an
atmospheric OH concentration of 1.0 x 106 molecule/cm3, the reported half-life of methyl
cellosolve is 0.64 d (Grosjean, 1997).
Chemical/Physical. At an influent concentration of 1,000 mg/L, treatment with GAC resulted in
an effluent concentration of 342 mg/L. The adsorbability of the carbon used was 132 mg/g carbon
(Guisti et al., 1974). | [Purification Methods]
Peroxides can be removed by refluxing with stannous chloride or by filtration under slight pressure through a column of activated alumina. 2-Methoxyethanol can be dried with K2CO3, CaSO4, MgSO4 or silica gel, then distilled from sodium. Aliphatic ketones (and water) can be removed by making the solvent 0.1% in 2,4-dinitrophenylhydrazine and allowing to stand overnight with silica gel before fractionally distilling. [Beilstein 1 IV 2375.] | [Toxicity evaluation]
High acute doses of methoxyethanol have a sedative and
hypnotic effect. Kidney and lung damages, accompanied by
hemoglobinuria, follow exposures to high doses. Toxicity is
attributed to the active metabolites: methoxyacetaldehyde and
methoxyacetate. In vitro studies with radiolabeled methoxyethanol
indicate that formation of methoxyacetyl-coenzyme A
may lead to the formation of methoxyacetyl derivatives of
Krebs cycle intermediates. Methoxyacetate produces the same
testicular lesions in rodents as does the parent compound,
although the immunosuppression elicited by methoxyethanol
exposure may depend on the putative metabolite, methoxyacetaldehyde.
In both the testicular lesion and the immune
suppression, some data suggest that the pattern of cell death
termed ‘apoptosis’ may be stimulated. Methoxyacetate stimulates
synthesis of progesterone by luteal cells in culture. This
disturbance of luteal function may be related to the prolongation
of gestation in rodents. Teratogenicity appears to be
related to interference by methoxyethanol, or its metabolites,
with one carbon metabolism in the synthesis of nucleotide
precursors, and can be relieved by administration of other
substrates, such as serine and glycine, which also provide
substrates for nucleotide synthesis. It has also been suggested
that toxicity is mediated through inhibition of flavoprotein
dehydrogenase-catalyzed reactions. |
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