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3-(Maleimido)propionic acid N-hydroxysuccinimide ester_Molecular_structure_CAS_55750-62-4)
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3-(Maleimido)propionic acid N-hydroxysuccinimide ester

Catalog No. 63179 Name Sigma Aldrich
CAS Number 55750-62-4 Website http://www.sigmaaldrich.com
M. F. C11H10N2O6 Telephone 1-800-521-8956
M. W. 266.2069 Fax
Purity ≥98.5% (HPLC) Email
Storage Chembase ID: 66715

SYNONYMS

IUPAC name
2,5-dioxopyrrolidin-1-yl 3-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)propanoate
IUPAC Traditional name
2,5-dioxopyrrolidin-1-yl 3-(2,5-dioxopyrrol-1-yl)propanoate
Synonyms
N-Maleoyl-β-alanine N′-hydroxysuccinimide ester
N-(3-Maleimidopropionyloxy)succinimide
BMPS
N-Succinimidyl 3-maleimidopropionate
3-(Maleimido)propionic acid N-succinimidyl ester

DATABASE IDS

MDL Number MFCD00043141
CAS Number 55750-62-4
PubChem SID 24882447
Beilstein Number 1492578

PROPERTIES

Empirical Formula (Hill Notation) C11H10N2O6
Purity ≥98.5% (HPLC)
Melting Point 167-171 °C
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261
Risk Statements 37
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (English)
Other Notes
Aliphatic cross-linking reagent of hetero-bifunctional type. Acylation at pH 8 proceeds most selectively whereas the stability of the maleimido group is much better compared to aromatic derivative 1 Used for the cross-linking of haptens to enzymes prior to enzyme immunoassays or fluorogenic substrates to peptidic antigens for use in fluorescence immunoassays 2
Description (简体中文)
Other Notes
Aliphatic cross-linking reagent of hetero-bifunctional type. Acylation at pH 8 proceeds most selectively whereas the stability of the maleimido group is much better compared to aromatic derivative 1 Used for the cross-linking of haptens to enzymes prior to enzyme immunoassays or fluorogenic substrates to peptidic antigens for use in fluorescence immunoassays 2

REFERENCES