N-Succinimidyl maleimidoacetate

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CAS:55750-61-3
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CAS:55750-61-3
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Products Intro: Product Name:N-Succinimidyl maleimidoacetate
CAS:55750-61-3
Purity:0.98 Package:1kg,2kg,5kg,10kg,25kg

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N-Succinimidyl maleimidoacetate Basic information
Product Name:N-Succinimidyl maleimidoacetate
Synonyms:MALEIMIDOACETIC ACID N-HYDROXYSUCCINIMIDE ESTER;N-SUCCINIMIDYL MALEIMIDOACETATE;a-Maleimidoacetic acid-NHS;N-(α-Maleimidoacetoxy)succinimide Ester(AMAS);1-[2-[(2,5-Dioxo-1-pyrrolidinyl)oxy]-2-oxoethyl]-1H-pyrrole-2,5-dione;N-(α-MaleiMidoacetoxy)succiMide;1H-Pyrrole-2,5-dione, 1-[2-[(2,5-dioxo-1-pyrrolidinyl)oxy]-2-oxoethyl]-;a-MaleiMidoacetic acid-NHS(AMAS)
CAS:55750-61-3
MF:C10H8N2O6
MW:252.18
EINECS:
Product Categories:Nitric Oxide Reagents;Cross Linking Reagents;Maleimide Derivatives;Crosslinking;Heterobifunctional Cross-Linking Reagents;Protein Modification;Cross Linking Reagents,Maleimide Derivatives;MTS & Sulfhydryl Active Reagents
Mol File:55750-61-3.mol
N-Succinimidyl maleimidoacetate Structure
N-Succinimidyl maleimidoacetate Chemical Properties
Melting point 174-175°C
Boiling point 430.1±47.0 °C(Predicted)
density 1.63±0.1 g/cm3(Predicted)
storage temp. Inert atmosphere,Store in freezer, under -20°C
solubility Chloroform (Slightly), DMSO (Slightly), Ethyl Acetate (Slightly, Heated)
form Solid
pka-2.69±0.20(Predicted)
color White to Off-White
InChIInChI=1S/C10H8N2O6/c13-6-1-2-7(14)11(6)5-10(17)18-12-8(15)3-4-9(12)16/h1-2H,3-5H2
InChIKeyTYKASZBHFXBROF-UHFFFAOYSA-N
SMILESN1(CC(ON2C(=O)CCC2=O)=O)C(=O)C=CC1=O
CAS DataBase Reference55750-61-3
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
HS Code 29280000
MSDS Information
ProviderLanguage
SigmaAldrich English
N-Succinimidyl maleimidoacetate Usage And Synthesis
Chemical PropertiesWhite Crystalline Solid
UsesA hetero-bifunctional cross-linking reagent for the preparation of protein-protein or protein-hapten conjugates.
UsesMaleimidoacetic acid N-hydroxysuccinimide ester is a crosslinking reagent that contains NHS ester- and maleimide-reactive groups at the opposite ends of a 4.4 ? spacer arm. This configuration allows for sequential, two-stage conjugation with amine and sulfhydryl functional groups in the preparation of protein-hapten or protein-protein conjugates.
Tag:N-Succinimidyl maleimidoacetate(55750-61-3) Related Product Information
Chloromethyl ethyl carbonate Diisopropyl chlorophosphate ETHYL CHLOROSULFONATE Suberate Bis(sulfosuccinimidyl) Sodium Salt BUTYL OLEATE Ethyl 2-(Chlorosulfonyl)acetate Maleimide Methyl acrylate O-Phthalimide N-Chlorosuccinimide N-Hydroxysuccinimide Tris(trimethylsilyl)phosphate Succinimide Bismaleimide DIALIFOS 1-(2-HYDROXY-ETHYL)-PYRROLE-2,5-DIONE 2-Maleimido acetic acid AC-GLY-OSU