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Monoethylene Glycol (Meg)
Monoethylene Glycol (Meg)
SDS Reference No. DSD-07-0001 REV NO. 1.1: October 01, 2016 Page 1 of 14
1.2 Relevant identified uses of the substance or mixture and uses advised against
IDENTIFIED USES:
Manufacturing of substance
Use as intermediate
Use as process chemical
Distribution of substance
Formulation and (re)packing of substances and mixtures
Production of polymers
Use in Paints/Coatings (Industrial)
Use in Paints/ Coatings /Adhesives/ Sealants/ Foams/ Polymers / filled Polymers (professional)
Use in Paints/ Coatings / Surface treatment products (Consumer use)
Use in Cleaning Agents (Industrial)
Use in Cleaning agents (professional)
Use in Cleaning agents (Consumer use)
Use in Lubricants (Industrial)
Use in metal-working fluids (Industrial)
Use in metal-working fluids (professional)
Use in agrochemicals (professional)
Use in/as functional fluids (industrial)
Use in/as functional fluids (professional)
Use in heat transfer and hydraulic fluids (Consumer use)
Use in/as de-icing/anti-icing applications/agents (professional)
Use in/as de-icing/anti-icing applications/agents (Consumer use)
Use in laboratories (industrial and professional)
Use in Laboratory (Industrial and Professional)
Use in water-treatment Chemicals (Industrial)
Use in adhesives and sealants (Consumer)
Production of Polymers, Filled Polymers, Foams, Coatings, Adhesives, Sealants
Production of rigid foam
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Impurities:
Impurity Identifiers Typical Classification Type
concentration 67/548/EEC Regulation (EC) No. 1272/2008
[CLP]
2,2’-oxydiethanol EC: 203-872-2 <0.01% (w/w) Not applicable Not applicable [B]
There are no additional ingredients present which, within the current knowledge of the supplier, are classified and contribute to the
classification of the substance and hence require reporting in this section.
Type: [A] Constituent [B] Impurity [C] Stabilizing additive
Occupational exposure limits, if available, are listed in Section 8.
4.2 Most important symptoms and effects, both acute and delayed
Potential acute health effects
Eye contact No relevant human information is available.
Inhalation No relevant human information is available.
Conform to Regulation (EC) No. 1907/2006 of the European Parliament and of the Council on the Registration,
Evaluation, Authorization and Restriction of Chemicals (REACH), Annex II -Europe
SAFETY DATA SHEET PR/EHD/OH/F-313
SDS Reference No. DSD-07-0001 REV NO. 1.1: October 01, 2016 Page 4 of 14
4.3 Indication of any immediate medical attention and special treatment needed
Notes to physician Treat symptomatically. Contact poison treatment specialist immediately if large quantities have been
ingested or inhaled
Specific treatments No specific treatment
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Flammability (solid, gas): non flammable upon ignition. Flammability derived from flash point.
Burning time: not applicable The substance has no pyrophoric properties and does not
Burning rate: not applicable liberate flammable gases on contact with water.
Upper/lower flammability Lower: 1.8%
or explosive limits: Upper: 12.8%
Vapour density: 2.14 [Air=1]
Viscosity: Dynamic: 20mPa.s
Auto-ignition temperature: not available
Explosive properties: non explosive Value used for CSA: non explosive
There are no chemical groups associated with explosive
properties present in the molecule.
Self-ignition temperature 398ºC
Decomposition temperature: Not available
Oxidising properties: No oxidising properties Value used for CSA: Oxidising: no
The substance is incapable of reacting exothermically with
combustible materials on the basis of the chemical structure
Viscosity: 16.1mPas at 25ºC
Stability in organic solvents and not applicable
identity or relevant degradation
products
Dissociation constant not applicable
Granulometry not applicable The substance is marketed or used in a non solid or granular
form.
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Corrosivity
Conclusion/Summary: The substance has shown to be not irritating for non-human
The substance has shown to be not irritating for human
Irritation: skin
Product/ingredient name Species Results Dose Exposures
ethanediol rabbit (Vienna White) not irritating; fully - 8 days
reversible
rabbit; Draize Test not irritating - 23 hours
Irritation: eyes
Product/ingredient name Species Results Dose Exposures
ethanediol rabbit (Vienna White) Not irritating; fully No data 24 hours
reversible
Conform to Regulation (EC) No. 1907/2006 of the European Parliament and of the Council on the Registration,
Evaluation, Authorization and Restriction of Chemicals (REACH), Annex II -Europe
SAFETY DATA SHEET PR/EHD/OH/F-313
SDS Reference No. DSD-07-0001 REV NO. 1.1: October 01, 2016 Page 9 of 14
Sensitisation
Product/ingredient name Species Results Dose Exposures
ethanediol guinea pig (Dunkin not sensitizing; No data 24 hours after challenge
Hartley) female no; with positive
reactions
human female No data No data No data
Patch Test
Conclusion/Summary: No structural alert; no testing necessary. In some orientating studies with animals and humans no
sensitizing properties were found.
Mutagenicity
Product/ingredient name Method Results Dose
ethanediol In vitro- bacterial reverse mutation assay Negative Doses: 0, 20, 100, 500,
(e.g. Ames test) (gene mutation): 2500, 5000 µg/plate
S. typhimurium TA 1535, TA 1537, TA 98 and
TA 100 (met. act.: with and without)
In vitro mammalian cell gene mutation Negative up to 5000 µg/ml
assay (gene mutation):
mouse lymphoma L5178Y cells
(met. act.: with and without metabolic
activation)
in vitro mammalian chromosome Negative 10 - 100 mg/ml
aberration test (chromosome
aberration):
Chinese hamster Ovary (CHO)
(met. act.: with and without metabolic
activation)
In vivo dominant lethal assay Negative 0.04, 0.2, 1.0 g/kg bw /day
(chromosome aberration)
rat (Fischer 344) male/female
oral: feed
Conclusion/summary: No relevant human information is available
Carcinogenicity
Product/ingredient name Method Results Dose
ethanediol rat (Fischer 344) male/female NOAEL (carcinogenicity): 0.04, 0.2, 1.0 g/kg bw /day
oral: feed (nominal in diet) 1000 mg/kg bw/day
Assessing the potential oncogenicity
and chronic toxicity when fed to rats
Exposure: 24 months (daily) for two years.
mouse (B6C3F1) male/female NOAEL (carcinogenicity): male mice: 0, 6250,
oral: feed 1500 mg/kg bw/day (male) 12500, 25000ppm;
Exposure: 103 weeks (daily) (liver histopathology)
female mice: 0, 12500,
25000, 50000ppm
(nominal in diet)
mouse (CD-1) male/female no NOAEL identified : (No 0.04, 0.2 or 1.0 g/kg bw
oral: feed clear NOAEL was (nominal diet)
Exposure: 24 months (daily) identified
Assessing oncogenicity and effects on
survival when fed to mice for 2 years.
Conclusion/summary: No information available for carcinogenicity via inhalation, dermal or other exposure routes
Conform to Regulation (EC) No. 1907/2006 of the European Parliament and of the Council on the Registration,
Evaluation, Authorization and Restriction of Chemicals (REACH), Annex II -Europe
SAFETY DATA SHEET PR/EHD/OH/F-313
SDS Reference No. DSD-07-0001 REV NO. 1.1: October 01, 2016 Page 10 of 14
Reproduction Toxicity
Effects on fertility
Product/ingredient name Method Results Dose
ethanediol rat (Fischer 344) male/female NOAEL (parental and 0.04, 0.2, 1.0 g/kg bw /day
three-generation study offspring): > 1000 mg/kg (nominal in diet)
oral: feed bw/day (male/female)
Exposure: 3 generations (daily) (There were no
reproductive effects
associated with the
inclusion of as much as
1.0 g/kg/day of
EO in the diet.)
mouse (CD-1) male/female NOEL (P): 1000 mg/kg ca. 500, 1000 and 2000
fertility bw/day (male/female)
oral: drinking water
NOEL (F1): 1000 mg/kg
bw/day (male/female)
Conclusion/summary: No information available for carcinogenicity via inhalation, dermal or other exposure routes
No relevant human information is available
Toxicity of reproduction
Developmental toxicity
Product/ingredient name Method Results Dose
ethanediol rat (COBS CD (SD)BR) NOAEC (maternal 0, 150, 1000 or 2500
inhalation: aerosol (whole body) toxicity): 1000 mg/m³ air ( mg/m3
Exposure: g.d. 6 - 15 (6 h/day) NOAEC (developmental
toxicity): 150 mg/m³ air
(NOAEC from inhalation
exposure alone cannot be
determined due to
confounding oral exposure
during whole-body
exposure.
rat (Sprague-Dawley) NOEL (maternal toxicity): 0, 150, 500, 1000 or 2500
oral: gavage 1000 mg/kg bw/day mg/kg bw /day
Exposure: g.d. 6 - 15 (daily) NOEL (developmental
toxicity): 500 mg/kg
bw/day
rat (Sprague-Dawley) NOAEL (maternal toxicity): 0, 250, 1250, 2250 mg/kg
oral: gavage 250 mg/kg bw/day (overall bw/d
Exposure: g.d. 6 - 20 (daily) effects)
NOAEL (developmental
toxicity): 250 mg/kg
bw/day (overall effects)
rabbit (New Zealand White) NOAEL (maternal toxicity): 0, 100, 500, 1000, 2000
oral: gavage 1000 mg/kg bw/day mg/kg/day
Exposure: g.d. 6 - 19 (daily NOAEL (developmental (nominal conc.)
toxicity): 2000 mg/kg
bw/day
mouse (CD-1) NOAEC (maternal 0, 150, 1000 or 2500
inhalation: aerosol (whole body) toxicity): mg/m3
Exposure: g.d. 6 - 15 (6 h/day) 150 mg/m³ air (Evidence of
maternal and embryofetal
toxicity, including
teratogenicity, was
observed
at 1000 and 2500 mg/m3.
Conform to Regulation (EC) No. 1907/2006 of the European Parliament and of the Council on the Registration,
Evaluation, Authorization and Restriction of Chemicals (REACH), Annex II -Europe
SAFETY DATA SHEET PR/EHD/OH/F-313
SDS Reference No. DSD-07-0001 REV NO. 1.1: October 01, 2016 Page 11 of 14
Teratogenicity
Aspiration hazards
Hazards: No relevant human or non-human information is available
Information on the likely No relevant human or non-human information is available
routes of exposure:
Delayed and immediate effects and also chronic effects from short and long term exposure
Short-term exposure
Potential immediate effects: No relevant human or non-human information is available
Potential delayed effects: No relevant human or non-human information is available
Long-term exposure
Conform to Regulation (EC) No. 1907/2006 of the European Parliament and of the Council on the Registration,
Evaluation, Authorization and Restriction of Chemicals (REACH), Annex II -Europe
SAFETY DATA SHEET PR/EHD/OH/F-313
SDS Reference No. DSD-07-0001 REV NO. 1.1: October 01, 2016 Page 12 of 14
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should be consulted for any available use-specific information provided in the Exposure Scenario(s).
13.1 Waste treatment methods
Product
Methods of disposal: The generation of waste should be avoided or minimized wherever possible. Significant quantities of
waste product residues should not be disposed of via the foul sewer but processed in a suitable effluent
treatment plant. Dispose of surplus and non-recyclable products via a licensed waste disposal
contractor. Disposal of this product, solutions and any by-products should at all times comply with the
requirements of environmental protection and waste disposal legislation and any regional local authority
requirements.
Hazardous waste: The classification of the product may meet the criteria for a hazardous waste.
Packaging
Methods of disposal: The generation of waste should be avoided or minimized wherever possible. Waste packaging should
be recycled. Incineration or landfill should only be considered when recycling is not feasible.
Special precautions: This material and its container must be disposed of in a safe way. Care should betaken when handling
emptied containers that have not been cleaned or rinsed out. Empty containers or liners may retain some
product residues. Avoid dispersal of spilt material and runoff and contact with soil, waterways, drains
and sewers.
14.1 UN number Not regulated. Not regulated. Not regulated. Not regulated.
14.6 Special precautions for Not available. Not available. Not available. Not available.
user
Additional information - - - -
Annex XVII – Restrictions on the manufacture, placing on the market and use of certain dangerous substances, mixtures and
articles: Not applicable
Other EU regulations
Europe inventory: All components are listed or exempted.
Black List Chemicals: Not listed
Priority List Chemicals: Not listed
Integrated pollution prevention and control list (IPPC) - Air: Not listed
Integrated pollution prevention and control list (IPPC) - Water: Not listed
International regulations
Chemical Weapons Convention List Not listed
Schedule I Chemical:
Conform to Regulation (EC) No. 1907/2006 of the European Parliament and of the Council on the Registration,
Evaluation, Authorization and Restriction of Chemicals (REACH), Annex II -Europe
SAFETY DATA SHEET PR/EHD/OH/F-313
SDS Reference No. DSD-07-0001 REV NO. 1.1: October 01, 2016 Page 14 of 14
Harmful if swallowed.
Full text of abbreviated H H302
statements: May cause damage to organs through prolonged or repeated exposure if
H373o
swallowed
Full text of Acute Tox. 4, H302 ACUTE TOXICITY: ORAL - Category 4
classifications[CLP/GHS]:
STOT Rep. Exp. 2, SPECIFIC TARGET ORGAN TOXICITY (REPEATEDEXPOSURE): ORAL
H373o [kidneys] - Category 2
Full text of abbreviated R
R22- Harmful if swallowed.
phrases
Full text of Xn - Harmful
classifications[DSD/DPD]
Version 1.1
Date of printing 10/01/2016
Date of previous issue 6/21/2011 (Revision 1.0)
DISCLAIMER: The information is based on our current and best knowledge and is intended to describe the product for
the purpose of health, safety and environmental requirements only. It should not therefore be construed
as guaranteeing any specific property of the product. Petro Rabigh makes no warranty of any kind,
expressed or implied, regarding the accuracy of these data. Petro Rabigh assumes no responsibility for
injury from the use of the product described herein.