General Description
Clear colorless liquid. Denser than water.
Reactivity Profile
ETHYL METHANESULFONATE(62-50-0) alkylates nucleophiles such as hydroxy, amino and sulfhydryl groups in model and biological materials. Is hydrolyzed by excess aqueous alkali to non-corrosive and non-toxic products. Is hydrolyzed by water to a highly corrosive product .
Air & Water Reactions
Water soluble.
Potential Exposure
Used as a research tool for mutagenesis and carcinogenesis studies. Was considered as a possible
human male contraceptive. Also considered as a reversible
male hemosterilant for insects and mammalian pests.
Fire Hazard
This chemical is combustible.
First aid
Skin Contact: Flood all areas of body that
have contacted the substance with water. Don’t wait to
remove contaminated clothing; do it under the water
stream. Use soap to help assure removal. Isolate contaminated clothing when removed to prevent contact by others.
Eye Contact: Remove any contact lenses at once. Flush
eyes well with copious quantities of water or normal saline
for a least 2030 minutes. Seek medical attention.
Inhalation: If convulsions are not present, give a glass or
two of water or milk to dilute the substance. Assure that
the person’s airway is unobstructed and contact a hospital
or poison center immediately for advice on whether or not
to induce vomiting. Ingestion: If convulsions are not present, give a glass or two of water or milk to dilute the substance. Assure that the person’s airway is unobstructed and
contact a hospital or poison center immediately for advice
on whether or not to induce vomiting eyes well with copious quantities of water or normal saline
for at least 2030 minutes. Seek medical attention.
Inhalation: Leave contaminated area immediately; breathe
fresh air. Proper respiratory protection must be supplied to
any rescuers. If coughing, difficult breathing or any other
symptoms develop, seek medical attention at once, even
if symptoms develop many hours after exposure. Ingestion:
If convulsions are not present, give a glass or two of water
or milk to dilute the substance. Assure that the person’s airway is unobstructed and contact a hospital or poison center
immediately for advice on whether or not to induce
vomiting
Shipping
UN2810 Toxic liquids, organic, n.o.s., Hazard
Class: 6.1; Labels: 6.1-Poisonous materials, Technical
Name Required. Military driver shall be given full and
complete information regarding shipment and conditions in
case of emergency. AR 50-6 deals specifically with the
shipment of chemical agents. Shipments of agent will be
escorted in accordance with AR 740-32.
Incompatibilities
Vapors may form explosive mixture with
air. Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep
away from alkaline materials, strong bases, strong acids,
oxoacids, and epoxides. Contact with moisture may cause
hydrolysis or other forms of decomposition
Chemical Properties
colourless liquid
Chemical Properties
Ethyl methane sulfonate is a clear liquid.
Uses
Ethyl methanesulfonate is used as mutagen for both mammalian and plant cells. It finds application as a model alkylating agent in the study of deoxyribonucleic acid (DNA) repair processes.
Uses
Experimentally as mutagen, teratogen and brain carcinogen.
Definition
ChEBI: A methanesulfonate ester resulting from the formal condensation of methanesulfonic acid with ethanol.
Biochem/physiol Actions
Ethyl methanesulfonate is a DNA ethylating agent, mutagenic to plants and animals and carcinogenic in mammals. It has been used as a model alkylating agent in studies of DNA repair processes. EMS induces base substitutions of guanine-cytosine (G/C) to adenine-thymine (A/T). EMS also generates point mutations and single nucleotide polymorphisms in genomes. EMS is potential chemical mutagen used for inducing mutation in rice, wheat and Arabidopsis thaliana.
Carcinogenicity
Ethyl methanesulfonate is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in experimental animals.