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Triethylene glycol monomethyl ether

HCID 8178
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Basic information

CAS
112-35-6
Standard SMILES
COCCOCCOCCO
InChIKey
JLGLQAWTXXGVEM-UHFFFAOYSA-N
Molecular formula
C7H16O4
Average molar mass
164.2 g/mol
Monoisotopic mass
164.10485899

Overview

Triethylene glycol methyl ether is a colorless odorless liquid. (USCG, 1999)

Names & identifiers

Preferred name
Triethylene glycol monomethyl ether
IUPAC
2-[2-(2-methoxyethoxy)ethoxy]ethanol
English name
Triethylene glycol monomethyl ether
Molecular formula
C7H16O4
Molecular weight
164.2

Names & synonyms

112-35-6TRIETHYLENE GLYCOL MONOMETHYL ETHER2-(2-(2-Methoxyethoxy)ethoxy)ethanolMethoxytriglycolMethyltrioxitol2-[2-(2-Methoxyethoxy)ethoxy]ethanolDowanol TMATMethoxytriethylene glycol3,6,9-Trioxa-1-decanolMethyl triethylene glycolTriglycol monomethyl etherTriethylene glycolmonomethyl ether
Show more names
MPEG3-OHTriethylene glycol monomethyl2-(2-(2-methoxyethoxy)ethoxy)-ethanoMETHYL TRIGLYCOL3,6,9-Trioxadecan-1-ol
Triethylene glycol methyl etherDTXSID5026912Ethanol, 2-[2-(2-methoxyethoxy)ethoxy]-DN0P4Q4I16Ethanol, 2-(2-(2-methoxyethoxy)ethoxy)-NSC-97395PEG-3 METHYL ETHERDTXCID506912

Database identifiers

CAS
112-35-6
PubChem CID
8178
DTXSID
DTXSID5026912
ChEMBL
CHEMBL1794613
ChEBI
CHEBI:84233
UNII
DN0P4Q4I16
EC Number
203-962-1
Nikkaji
J22.128G

Properties

Computed structural propertiesFilling in

XLogP
-1
Topological polar surface area
47.9 Ų
Hydrogen bond donors
1
Hydrogen bond acceptors
4
Rotatable bonds
8
Heavy atoms
11
Formal charge
0
Complexity
67.5

Experimental & physicochemical properties

SolventsSolvents -> Glycol Ethers (E Series)
CosmeticsCosmetic ingredients (PEG-3 Methyl Ether) -> CIR (Cosmetic Ingredient Review)
SpringerMaterials PropertiesSurface tension
SurfactantsSurfactant
LogP · 2 items

-1.46 (calculated)

-0.7

Density · 4 items

1.026 (USCG, 1999) - Denser than water; will sink

1.0494

Relative density (water = 1): 1.05

1.0494 @25 °C

Viscosity7 centistokes at 25 °C
Color/FormColorless liquid
Solubility · 4 items

In water, miscible

Soluble in water

Solubility in heptane = 1.5 wt%, completely soluble in acetone, benzene, ethyl ether, methanol, and carbon tetrachloride at 25 °C.

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

GHS classification

GHS Classification · 6 items

This chemical does not meet GHS hazard criteria for 88.1% (290 of 329) of all reports.

Warning

H315 (11.6%): Causes skin irritation [Warning Skin corrosion/irritation]

P264, P264+P265, P280, P302+P352, P305+P351+P338, P321, P332+P317, P337+P317, and P362+P364 (click each P-code to see the statement)

Aggregated GHS information provided per 329 reports by companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Not Classified

Hazard information

Regulatory Information · 4 items

Chemical: Ethanol, 2-[2-(2-methoxyethoxy)ethoxy]-

Ethanol, 2-[2-(2-methoxyethoxy)ethoxy]- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Ethanol, 2-[2-(2-methoxyethoxy)ethoxy]- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

Status: Active Update: 10-03-2023 https://echa.europa.eu/registration-dossier/-/registered-dossier/14921

Ethanol, 2-[2-(2-methoxyethoxy)ethoxy]-: Does not have an individual approval but may be used under an appropriate group standard

Fire HazardsCombustible.
Fire PotentialCombustible
Health HazardsNo appreciable hazard in ordinary handling or use. (USCG, 1999)
Hazards Summary · 1 item

In lethal-dose animal studies, causes liver injury; Oral doses of 4000 mg/kg/day for 91 days cause testicular injury in rats; Developmental toxicity is seen in rats receiving >1000 mg/kg/day; Genotoxic studies were negative; [OECD SIDS: 2-(2-(2-Methoxyethoxy)ethoxy)ethanol - 1996] No listed effects of short-term or long-term exposure; [ICSC] May form unstable peroxides in the presence of oxygen; [CAMEO] May cause mild skin and eye irritation; [eChemPortal: SIDSUNEP] See GLYCOL ETHERS.

Chemistry & industry

Pharmacology

Metabolism/Metabolites · 1 item

The main metabolic pathway for metabolism of TGME and TGEE (and presumably the category members) is oxidation via alcohol dehydrogenase that leads to the formation of an alkoxy acid. A second important route of metabolism is oxidation by P-450 mixed function oxidases (O-dealkylation) that lead to the formation of triethylene glycol (TEG). TEG may be oxidized to a carboxylic acid. The principal metabolite of TGME is believed to be 2-[2-(2-methoxyethoxy)ethoxy] acetic acid.

Absorption, Distribution and Excretion · 2 items

It is slowly absorbed through skin. Excessive exposure involving large areas of skin for extended periods of time would be required before serious effects would be expected.

The penetration of triethylene glycol monomethyl ether (TGME) through human skin was studied in vitro using the epidermis from human abdominal skin. An area of 2.54 sq cm was exposed in a glass diffusion apparatus for treatment. The diffusion rate for TGME is 34 ug/sq cm/hr.

Uses & manufacturing

Uses · 5 items

CIR ingredient: PEG-3 Methyl Ether

Used as coupling solvent (water-based paints), for blending brake and hydraulic fluids, and as a plasticizer and wetting agent (resins and paints); [HSDB] Used as raw material for automotive hydraulic brake fluids and a solvent in coatings, printing inks, cleaning products, cutting oils, and deicing agents; [eChemPortal: SIDSUNEP]

Metal Machining [Category: Heat or Machine]

Coupling solvent (water-based paints), brake/hydraulic fluid blending component, plasticizer/wetting agent (resins, paints), solvent.

A solvent and plasticizer intermediate.

U.S. Exports · 3 items

(1972) 2.27X10+9 GRAMS (ALL MONOETHERS)

(1975) 2.27X10+9 GRAMS (ALL MONOETHERS)

(1984) 7.53X10+10 g /Ethers of Polyhydric alcohols and their derivatives/

U.S. Imports · 2 items

Related reactions

89 records
New reaction record
HRID 6976 reaction equation
HRID 6976As reactantuspto-grants-2006_08
HRID 39208 reaction equation
HRID 39208As reactantuspto-grants-2013_09
HRID 78704 reaction equation
HRID 78704As reactantuspto-grants-2014_09
HRID 128351 reaction equation
HRID 128351As reactantuspto-grants-1981_03
HRID 180800 reaction equation
HRID 180800As reactantTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
HRID 206631 reaction equation
HRID 206631As reactantTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
HRID 220227 reaction equation
HRID 220227As reactantuspto-grants-2012_06
HRID 253675 reaction equation
HRID 253675As reactantuspto-grants-2011_01
Page 1 of 12

Compound notes

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Solubility in water: miscible

Flash Point · 3 items

greater than 230 °F (USCG, 1999)

245 °F (118 °C) (OPEN CUP)

114.4 °C c.c.

Boiling Point · 3 items

246 °C

249 °C

249 °C @760 [mm Hg]

DecompositionWhen heated to decomposition it emits acrid smoke and irritating fumes.

Physicochemical properties

Melting point
-45 °C · -45 °C
Boiling point
248 °C · 248 °C
Density
1.05 · 1.05
vapor density
5.66 · 5.66 (vs air)
vapor pressure
0.01 mm · <0.01 mm Hg ( 20 °C)
refractive index
1.44 · 1.44
Flash point
134 °C · 134 °C
storage temp.
30 °C · Store below +30°C.
Water Solubility
Completely miscible in water
form
clear liquid
pka
14.36 · 14.36±0.10(Predicted)
color
Colorless
PH
5 · 5-7 (H2O, 20℃)
BRN
1700198 · 1700198
Henry's Law Constant
2.8 · 2.8×108 mol/(m3Pa) at 25℃, HSDB (2015)
Cosmetic Ingredient Review (CIR)
TRIETHYLENE GLYCOL MONOMETHYL ETHER (112-35-6)
InChI
1S/C7H16O4/c1-9-4-5-11-7-6-10-3-2-8/h8H,2-7H2,1H3
InChIKey
JLGLQAWTXXGVEM-UHFFFAOYSA-N
SMILES
COCCOCCOCCO
LogP
-1.12 at · -1.12 at 20℃
CAS DataBase Reference
112 · 112-35-6(CAS DataBase Reference)
EWG's Food Scores
1 · 1-3
FDA UNII
0 P4Q4I16 · DN0P4Q4I16
NIST Chemistry Reference
2 · Ethanol, 2-[2-(2-methoxyethoxy)ethoxy]-(112-35-6)
EPA Substance Registry System
Triethylene glycol monomethyl ether (112-35-6)
UNSPSC Code
12352104 · 12352104
NACRES
23 · NA.23
Symbol(GHS)
7 · GHS07
Signal word
Warning
Hazard statements
315 · H315-H319
Precautionary statements
305 · P305+P351+P338
PPE
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
Safety Statements
24 · 24/25-22
WGK Germany
1 · 1
RTECS
6390000 · KL6390000
F
10 · 10-23
Autoignition Temperature
210 °C · 210 °C
TSCA
TSCA listed
HS Code
2909499000 · 2909499000
Storage Class
10 · 10 - Combustible liquids
Hazardous Substances Data
112 · 112-35-6(Hazardous Substances Data)
Toxicity
50 orally · LD50 orally in Rabbit: 11850 mg/kg LD50 dermal Rabbit 7448 mg/kg
REACH Registrations
Active
Reactive GroupAlcohols and Polyols
TSCA Requirements · 3 items

Pursuant to section 8(d) of TSCA, EPA promulgated a model Health and Safety Data Reporting Rule. The section 8(d) model rule requires manufacturers, importers, and processors of listed chemical substances and mixtures to submit to EPA copies and lists of unpublished health and safety studies. Triethylene glycol monomethyl ether is included on this list.

Manufacturers and processors of triethylene glycol monomethyl ether are required to conduct developmental neurotoxicity tests under TSCA section 4.

A testing consent order is in effect for developmental neurotoxicity testing for triethylene glycol monomethyl ether for health effects testing. FR citation: April 3, 1989.

Reactivity AlertsPeroxidizable Compound
Reactivity Profile · 1 item

Ethers, such as TRIETHYLENE GLYCOL METHYL ETHER, can act as bases. They form salts with strong acids and addition complexes with Lewis acids. The complex between diethyl ether and boron trifluoride is an example. Ethers may react violently with strong oxidizing agents. In other reactions, which typically involve the breaking of the carbon-oxygen bond, ethers are relatively inert.

Chemical DangersOn combustion, forms toxic gases. Reacts with strong acids, strong bases and strong oxidants.
Air and Water Reactions · 1 item

Ethers tend to form unstable peroxides when exposed to oxygen. Ethyl, isobutyl, ethyl tert-butyl, and ethyl tert-pentyl ether are particularly hazardous in this respect. Ether peroxides can sometimes be observed as clear crystals deposited on containers or along the surface of the liquid.

NFPA Hazard Classification · 3 items

1 - Materials that, under emergency conditions, can cause significant irritation.

1 - Materials that must be preheated before ignition can occur. Materials require considerable preheating, under all ambient temperature conditions, before ignition and combustion can occur.

0 - Materials that in themselves are normally stable, even under fire conditions.

Safety & protection

Fire Fighting · 2 items

Fire Extinguishing Agents Not to Be Used: Water or foam may cause frothing.

Use powder, foam, carbon dioxide.

First Aid Measures · 4 items

Fresh air, rest.

Remove contaminated clothes. Rinse and then wash skin with water and soap.

Rinse with plenty of water (remove contact lenses if easily possible).

Rinse mouth. Give one or two glasses of water to drink.

First AidWash affected parts with water. (USCG, 1999)
Safe StorageSeparated from strong oxidants, strong bases and strong acids.
Exposure Control and Personal Protection50.0 [mg/m3]. inhalable fraction[German Research Foundation (DFG)]
Disposal Methods · 1 item

SRP: The most favorable course of action is to use an alternative chemical product with less inherent propensity for occupational exposure or environmental contamination. Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air quality; potential migration in soil or water; effects on animal, aquatic, and plant life; and conformance with environmental and public health regulations.

Spillage DisposalCollect leaking liquid in covered containers. Then store and dispose of according to local regulations. Wash away spilled liquid with plenty of water.
Eye PreventionWear safety spectacles.
Fire PreventionNO open flames.
Inhalation RiskA harmful contamination of the air will not or will only very slowly be reached on evaporation of this substance at 20 °C.
Skin PreventionProtective gloves.
Exposure PreventionPREVENT GENERATION OF MISTS!

Toxicology

Ecotoxicity Values · 2 items

LC50 Daphnia magna (Water flea) >10000 mg/L/48 hr /Conditions of bioassay not specified in source examined/

LC50 Pimephales promelas (Fathead minnow) >10000 mg/L/96 hr /Conditions of bioassay not specified in source examined/

Environmental Fate · 3 items

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 10(SRC), determined from a structure estimation method(2), indicates that triethylene glycol monomethyl ether is expected to have very high mobility in soil(SRC). Volatilization of triethylene glycol monomethyl ether from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 3.5X10-14 atm-cu m/mole(SRC), using a fragment constant estimation method(3). Triethylene glycol monomethyl ether is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 3.5X10-3 mm Hg(SRC), determined from a fragment constant method(4). Triethylene glycol monomethyl ether has percent theoretical BOD values of 14 and 23 at 10 and 20 days, respectively(5), which suggest that biodegradation is not an important environmental fate process in soil(SRC).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 10(SRC), determined from a structure estimation method(2), indicates that triethylene glycol monomethyl ether is not expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is not expected(3) based upon an estimated Henry's Law constant of 3.5X10-14 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). According to a classification scheme(5), an estimated BCF of 3(SRC), from an estimated log Kow of -1.46(6) and a regression-derived equation(7), suggests the potential for bioconcentration in aquatic organisms is low(SRC). Triethylene glycol monomethyl ether has percent theoretical BOD values of 14 and 23 at 10 and 20 days, respectively(8), which suggest that biodegradation is not an important environmental fate process in water(SRC).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), triethylene glycol monomethyl ether, which has an estimated vapor pressure of 3.5X10-3 mm Hg at 25 °C(SRC), determined from a fragment constant method(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase triethylene glycol monomethyl ether is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 9.6 hours(SRC), calculated from its rate constant of 4X10-11 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3).

Adverse EffectsNeurotoxin - Acute solvent syndrome
Toxicity Summary · 2 items

The CIR Expert Panel concluded that the alkyl PEG ethers, listed below, are safe in the present practices of use and concentration described in this safety assessment when formulated to be nonirritating. This assessment is also intended to address future alkyl PEG ether cosmetic ingredients that vary from those ingredients recited herein only by the number of ethylene glycol repeat units...PEG-3 Methyl Ether...

Safe for use in cosmetics, with qualifications

Effluent ConcentrationsTriethylene glycol monomethyl ether was listed as a contaminant found in advanced treatment water in Lake Tahoe, CA(1).
ICSC Environmental DataEnvironmental effects of the substance have been adequately investigated, but no significant effects have been found.
Soil Adsorption/Mobility · 1 item

Using a structure estimation method based on molecular connectivity indices(1), the Koc of triethylene glycol monomethyl ether can be estimated to be 10(SRC). According to a classification scheme(2), this estimated Koc value suggests that triethylene glycol monomethyl ether is expected to have very high mobility in soil(SRC).

TSCA Test Submissions · 5 items

Acute oral toxicity was evaluated in groups of 10 male albino Wistar rats administered single doses of undiluted Poly Solv TM (triethylene glycol monomethyl ether) by oral gavage at levels of 5.0, 7.12, 10.14, or 14.43 g/kg body weight. Mortality was observed in 1 animal in the 10.14 g/kg dose group, and in 8 animals in the highest dose group. The LD50 value was calculated to be 12.6 g/kg (10.4 to 15.3 g/kg 95% confidence limits) by the Litchfield and Wilcoxon method. Clinical observations included ataxia, piloerection, lethargy, blood in the anogenital area (1 rat), ptosis, and coma. Gross necropsy of animals in the highest dose group revealed yellow intestines with blood in the lumen, dark liver, and blood in the stomach.

Acute oral toxicity was evaluated in groups of 6 male rats (strain not reported) administered single doses of Dowanol TMH (triethylene glycol monomethyl ether) as a 20% solution in corn oil at levels of 0.5, 1.0, 2.0, and 3.98 g/kg body weight. Mortality was not observed and an LD50 value was not reported. Clinical findings and gross necropsy were not reported.

Acute oral toxicity was evaluated in groups of 5 male albino rats (strain not reported) administered single doses of undiluted methoxytriglycol by oral gavage at levels of 4.0, 8.0, and 16.0 mL/kg of body weight. Mortality was observed in all 5 animals in the 16.0 mL/kg dose group; the LD50 value was calculated to by 11.3 mL/kg by the moving average method. Clinical observations were not reported. Gross necropsy findings included congested lungs, mottled livers and kidneys, gastrointestinal tract irritation and slightly congested adrenals.

Acute dermal toxicity was evaluated in 10 New Zealand White rabbits receiving single occluded applications of Poly Solv TE (methoxy triethylene glycol) at a dose level of 2.0 g/kg of body weight. The test article was held in contact with the skin (half intact, half abraded) for a 24 hour period. Mortality was not observed. Clinical observations included dermal erythema and edema. Gross necropsy revealed mottled liver in 1 animal, white nodules in 2 animals, pocked kidneys in 2 animals, and dark lung areas in 1 animal.

For more TSCA Test Submissions (Complete) data for TRIETHYLENE GLYCOL MONOMETHYL ETHER (24 total), please visit the HSDB record page.

Human Toxicity Excerpts · 2 items

/EPIDEMIOLOGY STUDIES/ Ethylene glycol ethers (EGEs) including diglyme are used in the manufacture of semiconductors. Epidemiological studies of semiconductor populations evaluated potential adverse reproductive outcomes. ... In each of these studies, workers were exposed to mixtures including diglyme but not to diglyme alone. ... Exposure to EGEs was determined using questionnaires from subjects about the work performed and an assessment of the work environment by industrial hygienists, but no measurements of personal or area exposures were made. Workers in the fabrication area were considered exposed to EGEs. For the retrospective study, information on pregnancy outcomes and potential confounders (age, smoking, ethnicity, education, income, year of pregnancy, and stress) was obtained through a comprehensive interviewer-administered interview of female employees. The prospective study of early fetal loss and fecundity (probability of conception per menstrual cycle) was conducted in a subset of female employees from five plants. Daily diaries and measurements of daily urinary human chorionic gonadotrophin (hCG) levels for 6 months were collected in addition to the comprehensive interview. Of the 891 medically verified pregnancies identified for the retrospective study, 774 (86.9%) were live births, 113 (12.7%) were spontaneous abortions, and 4 (0.4%) were stillbirths. The overall unadjusted relative risk (RR) for spontaneous abortions was 1.45 (95% confidence interval [CI] = 1.02-2.05) and changed little after adjusting for confounders (adjusted RR =1.43; 95% CI = 0.95-2.09). When stratified by work group, the risk of spontaneous abortion was statistically significantly increased for female workers in the photolithography group (RR = 1.67; 95% CI = 1.04-2.55) and in the etching group (RR = 2.08; 95% CI = 1.27-3.19). For women working with higher levels of EGE only in masking, the risk for spontaneous abortion was increased 3-fold (RR = 3.38; 95% CI = 1.61-5.73). In the prospective study, no statistically significant differences were detected in the overall rate of spontaneous abortions between fabrication and non-fabrication workers or when pregnancy outcomes were examined by work group. However, the ability to conceive was lower among female workers exposed to EGEs (fertility rate [FR] = 0.37; 95% CI = 0.11-1.19). /Ethylene glycol ethers/

/BIOMONITORING/ In the present study, floor lacquerers' (n = 22) inhalation and total exposure to 2-(2-alkoxy)ethoxyethanols was measured. The measurements of inhalation exposure were done with charcoal tubes, and total exposure was biomonitored by urinalysis of 2-(2-alkoxyethoxy)acetic acids. The 8 hr inhalation exposures of floor lacquerers to 2-(2-methoxyethoxy)ethanol (DEGME), 2-(2-ethoxyethoxy)ethanol (DEGEE) and 2-(2-butoxyethoxy)ethanol (DEGBE) were in average 0.23 +/- 0.07 ppm (average +/-S.D., n = 3), 0.08 +/- 0.07 ppm (n = 16), and 0.05 +/- 0.03 ppm (n = 16), respectively. The excretions of 2-(2-methoxyethoxy)acetic acid (MEAA), 2-(2-ethoxyethoxy)acetic acid (EEAA) and 2-(2-butoxyethoxy)acetic acid (BEAA) were in average 4.9 +/- 4.3 mmol/mol creatinine, 9.3 +/- 8.0 mmol/mol creatinine and 9.2 +/- 7.4 mmol/mol creatinine, respectively. A linear relationship was found between the urinary 2-(2-alkoxyethoxy)acetic acid concentrations and the preceding 8-hr occupational exposure to 2-(2-alkoxyethoxy)ethanol.

Artificial Pollution Sources · 1 item

Triethylene glycol monomethyl ether's production and use as a plasticizer intermediate(1), coupling solvent, brake/hydraulic fluid blending component, wetting agent, and solvent may result in its release to the environment through various waste streams(SRC).

Environmental Biodegradation · 1 item

AEROBIC: Triethylene glycol monomethyl ether has 10 and 20 day theoretical BOD values of 14 and 23, respectively(1). A study using activated sludge gave a degradation rate for diethylene glycol monoethyl ether of 0.22/hour(2) giving a half-life of 3.2 hours(SRC).

Environmental Bioconcentration · 1 item

An estimated BCF of 3 was calculated in fish for triethylene glycol monomethyl ether(SRC), using an estimated log Kow of -1.46(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is low(SRC).

Regulatory information

TSCA Requirements · 3 items

Pursuant to section 8(d) of TSCA, EPA promulgated a model Health and Safety Data Reporting Rule. The section 8(d) model rule requires manufacturers, importers, and processors of listed chemical substances and mixtures to submit to EPA copies and lists of unpublished health and safety studies. Triethylene glycol monomethyl ether is included on this list.

Manufacturers and processors of triethylene glycol monomethyl ether are required to conduct developmental neurotoxicity tests under TSCA section 4.

A testing consent order is in effect for developmental neurotoxicity testing for triethylene glycol monomethyl ether for health effects testing. FR citation: April 3, 1989.

Safety data

F
10-23
PPE
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
wgk
1
tsca
TSCA listed
rtecs
KL6390000
hs_code
2909499000
Toxicity
LD50 orally in Rabbit: 11850 mg/kg LD50 dermal Rabbit 7448 mg/kg
Signal word
Warning
Symbol(GHS)
GHS07
safety_code
24/25-22
Storage Class
10 - Combustible liquids
Hazard statements
H315-H319
REACH Registrations
Active
Autoignition Temperature
210 °C
Precautionary statements
P305+P351+P338
Hazardous Substances Data
112-35-6(Hazardous Substances Data)

(1972) NEGLIGIBLE

(1975) NEGLIGIBLE

U.S. Production · 6 items

2023: 40,000,000 - <55,000,000 lb

(1972) 1.44X10+10 GRAMS

(1975) 1.77X10+10 GRAMS

(2006) 1,612 million lb annual capacity /Glycol ethers/

Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#2666]

This chemical is listed as a High Production Volume (HPV) (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and/or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B; 51FR21438).

Consumption Patterns(ALL TRIETHYLENE GLYCOL MONOETHERS) 95% AS A SOLVENT IN HYDRAULIC BRAKE FLUIDS; 5% AS A SOLVENT IN PROTECTIVE COATINGS, PRINTING INKS, & CHEMICAL SPECIALTIES (1972)
Consumer UsesLubricating agent
Industry UsesIntermediate
Methods of Manufacturing · 2 items

Ethylene glycol monoethers are commercially manufactured by reaction of an alcohol with ethylene oxide. /Ethylene Glycol Monoethers/

Ethylene glycol monoethers are usually produced by reaction of ethylene oxide with the appropriate alcohol. A mixture of homologues is obtained ... The glycol monoethers can be converted to diethers by alkylation with common alkylating agents, such as dimethyl sulfate or alkyl halides ( Williamson synthesis). Glycol dimethyl ethers are formed by treatment of dimethyl ether with ethylene oxide. /Ethers/

Household ProductsInformation on 17 consumer products that contain Methoxytriglycol in the following categories is provided:
General Manufacturing Information · 2 items

Printing and Related Support Activities

Ethanol, 2-[2-(2-methoxyethoxy)ethoxy]-: ACTIVE

Applications · 4 items

Descriptionm-PEG3-alcohol is a PEG linker containing a hydroxyl group. The hydroxyl group enables further derivatization or replacement with other reactive functional groups. The hydrophilic PEG spacer increases solubility in aqueous media.

UsesPlasticizer intermediate.

UsesTriethylene glycol monomethyl ether can be used as a reagent and solvent for applications such as: modification of anthraquinone material for redox flow batteriespreparation of polymeric electrolyte for electrochemical devices,formation of the binary system of polyethylene glycol for absorption of silica.

General DescriptionColorless odorless liquid.

Upstream & downstream products

Upstream raw materials

Ethylene oxideMethanol

Downstream products

Nonaethylene Glycol Monomethyl EtherDiethylene glycol monomethyl etherMethyltriglycolmethacrylatem-PEG7-OTs2,5,8,11,14,17-Hexaoxanonadecan-19-ol, methanesulfonatem-PEG3-Tos2-(2-(2-Methoxyethoxy)ethoxy)ethyl 4-Methylbenzenesulfonate2,5,8,11,14,17-Hexaoxanonadecan-19-amineHexaethylene Glycol Monomethyl EtherDioctyl maleate2,2-dimethyl-3,6,9,12-tetraoxa-2-silatridecaneTri(ethylene glycol) methyl vinyl ether, 98

Additional notes

DefinitionChEBI: A hydroxypolyether that is the monomethyl ether derivative of triethylene glycol. Metabolite observed in cancer metabolism.