Ethyl methanesulfonate

Ethyl methanesulfonate Basic information
Product Name:Ethyl methanesulfonate
Synonyms:CB 1528;EMS;ENT 26396;ent26396;Ethyl ester of methanesulfonic acid;Ethyl ester of methanesulphonic acid;Ethyl ester of methylsulfonic acid;Ethyl ester of methylsulphonic acid
CAS:62-50-0
MF:C3H8O3S
MW:124.16
EINECS:200-536-7
Product Categories:
Mol File:62-50-0.mol
Ethyl methanesulfonate Structure
Ethyl methanesulfonate Chemical Properties
Melting point <25 °C
Boiling point 85-86 °C/10 mmHg (lit.)
density 1.206 g/mL at 20 °C
vapor pressure 0.27 hPa (25 °C)
refractive index n20/D 1.418(lit.)
Fp 100 °C
storage temp. 2-8°C
solubility 50-100g/l
form liquid
color Colourless to Pale Yellow
Water Solubility Miscible with water.
Sensitive Moisture Sensitive
Merck 14,3827
BRN 773969
Stability:Stable. Combustible. Incompatible with water, alkalies, oxidizing agents.
InChIKeyPLUBXMRUUVWRLT-UHFFFAOYSA-N
CAS DataBase Reference62-50-0(CAS DataBase Reference)
IARC2B (Vol. 7, Sup 7) 1987
NIST Chemistry ReferenceMethanesulfonic acid, ethyl ester(62-50-0)
EPA Substance Registry SystemEthyl methanesulfonate (62-50-0)
Safety Information
Hazard Codes T
Risk Statements 46-22-40-36/37/38-45
Safety Statements 53-23-36/37/39-45-36/37-37/39-26
RIDADR 2810
WGK Germany 3
RTECS PB2100000
10-21
TSCA Yes
HazardClass 6.1
PackingGroup II
HS Code 29041000
Hazardous Substances Data62-50-0(Hazardous Substances Data)
MSDS Information
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Ethyl methanesulfonate English
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Ethyl methanesulfonate Usage And Synthesis
Chemical Propertiescolourless liquid
Chemical PropertiesEthyl methane sulfonate is a clear liquid.
UsesExperimentally as mutagen, teratogen and brain carcinogen.
UsesEthyl 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.
DefinitionChEBI: A methanesulfonate ester resulting from the formal condensation of methanesulfonic acid with ethanol.
General DescriptionClear colorless liquid. Denser than water.
Air & Water ReactionsWater soluble.
Reactivity ProfileEthyl methanesulfonate 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 .
Fire HazardEthyl methanesulfonate is combustible.
Biochem/physiol ActionsEthyl 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.
Safety ProfileConfirmed carcinogen with experimental carcinogenic, neoplas tigenic, tumorigenic, and teratogenic data. Poison by ingestion and intraperitoneal routes. Experimental reproductive effects. Human mutation data reported. When heated to decomposition it emits toxic fumes of SOx. See also SULFONATES and ESTERS.
Potential ExposureUsed 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.
CarcinogenicityEthyl methanesulfonate is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in experimental animals.
ShippingUN2810 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.
IncompatibilitiesVapors 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
Ethyl methanesulfonate Preparation Products And Raw materials
Raw materialsMethanesulfonyl chloride
5'-Tosyladenosine 2-CHLOROETHYL P-TOLUENESULFONATE Tetrabromophenol Blue 1,6-ANHYDRO-3,4-O-ISOPROPYLIDENE-2-TOSYL-B-D-GALACTOPYRANOSE 1,3-Propane sultone Bromoxylenol Blue BTB 2,2,2-TRIFLUOROETHYL P-TOLUENESULFONATE Chlorophenol Red Bromophenol Blue Thymol Blue Phenol Red Ethyl trifluoromethanesulfonate P-XYLENOL BLUE Pyrocatechol Violet 3-CHLORO-3H-2,1-BENZOXATHIOLE-1,1-DIOXIDE Cresol Purple Bromocresol green Ethyl Mesylate

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