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128-53-0

N-Ethylmaleimide

CAS: 128-53-0

Molecular Formula: C6H7NO2

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128-53-0 - Names and Identifiers

Name N-Ethylmaleimide
Synonyms NEM
usafb-121
N-ETHYLMALEIMIDE
N-Ethylmaleimide
N-EthylmaleimideA.R.
N-Ethylmaleimide, (NEM)
N-ETHYLMALEIMIDE SIGMAULTRA
1-ethyl-1H-pyrrole-2,5-dione
1-ETHYL-1H-PYRROLE-2,5-DIONE
1-Ethyl-1H-pyrrole-2,5-dione~NEM
CAS 128-53-0
EINECS 204-892-4
InChI InChI=1/C6H7NO2/c1-2-7-5(8)3-4-6(7)9/h3-4H,2H2,1H3
InChIKey HDFGOPSGAURCEO-UHFFFAOYSA-N

128-53-0 - Physico-chemical Properties

Molecular FormulaC6H7NO2
Molar Mass125.13
Density1.2500 (rough estimate)
Melting Point43-46°C(lit.)
Boling Point210°C(lit.)
Flash Point73 °C
Water Solubility1 g/L (20 ºC)
Solubility methanol: 1M at20°C, clear, colorless
Vapor Presure0.197mmHg at 25°C
AppearanceCrystalline Powder
ColorWhite to off-white
Merck14,3822
BRN112448
pKa-2.18±0.20(Predicted)
Storage Condition2-8°C
StabilityStable. Combustible. Incompatible with strong oxidizing agents. Refrigerate.
SensitiveLight Sensitive
Refractive Index1.4430 (estimate)

128-53-0 - Risk and Safety

Hazard SymbolsT+ - Very toxic
Very toxic
Risk CodesR21 - Harmful in contact with skin
R28 - Very Toxic if swallowed
R34 - Causes burns
R43 - May cause sensitization by skin contact
R20/21 - Harmful by inhalation and in contact with skin.
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S28 - After contact with skin, wash immediately with plenty of soap-suds.
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S28A -
UN IDsUN 2928 6.1/PG 2
WGK Germany3
RTECSUX9625000
FLUKA BRAND F CODES19
TSCAYes
HS Code29251900
Hazard Class6.1
Packing GroupII

128-53-0 - Reference Information

biological activity N-Ethylmaleimide (NEM) is an organic compound derived from maleic acid. It is an irreversibility inhibitor of cysteine peptidases, alkylation of thiol groups at the active site. N-Ethylmaleimide (NEM) can inactivate endogenous deubiquitinating enzymes (DUBs). N-Ethylmaleimide (NEM) specifically inhibits phosphate transport in mitochondria.
target Cysteine protease
use 1, covalent modification reagent of protein cysteine residues. 2. Mercapto alkylation reagent inactivates NADP-dependent isocitrate dehydrogenase and many endonuclease enzymes. 3. Increase the current from the M-channel in the sympathetic neurons and act as an opener for KCNQ2, KCNQ4 and KCNQ5 channels.
NIST chemical information The information is: webbook.nist.gov provides (external link)
EPA chemical information The information is: offered by ofmpub.epa.gov (external link)
Last Update:2024-04-10 22:29:15
128-53-0
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Mobile: +86-17551318830
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