4-(Maleimidomethyl)cyclohexane-1-carboxylic acid N-hydroxysuccinimide ester

98%

  • Product Code: 77221
  Alias:    SMCC
  CAS:    64987-85-5
  Properties:    Chloroform: soluble 50 mg/mL DMF: soluble
Molecular Weight: 334.33 g./mol Molecular Formula: C₁₆H₁₈N₂O₆
EC Number: MDL Number: MFCD00009634
Melting Point: 180-182 °C(lit.) Boiling Point:
Density: Storage Condition: -20℃
Product Description: This compound is widely used in bioconjugation and protein labeling applications. Its maleimide group reacts selectively with thiol groups (-SH) in cysteine residues of proteins, enabling the attachment of biomolecules. The N-hydroxysuccinimide (NHS) ester moiety allows it to react with primary amines (-NH2) present in lysine residues or other amine-containing molecules, facilitating crosslinking or labeling. It is particularly useful in antibody-drug conjugates (ADCs), where it links antibodies to cytotoxic drugs, enhancing targeted cancer therapy. Additionally, it is employed in the preparation of biosensors, immobilization of enzymes, and the study of protein interactions. Its bifunctional nature makes it a versatile tool in biochemical research and therapeutic development.
Product Specification:
Test Specification
Purity 97.5 100%
APPEARANCE White to off-white powder
INFRARED SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.200 10-20 days ฿1,370.00
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1.000 10-20 days ฿5,200.00
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5.000 10-20 days ฿14,680.00
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4-(Maleimidomethyl)cyclohexane-1-carboxylic acid N-hydroxysuccinimide ester
This compound is widely used in bioconjugation and protein labeling applications. Its maleimide group reacts selectively with thiol groups (-SH) in cysteine residues of proteins, enabling the attachment of biomolecules. The N-hydroxysuccinimide (NHS) ester moiety allows it to react with primary amines (-NH2) present in lysine residues or other amine-containing molecules, facilitating crosslinking or labeling. It is particularly useful in antibody-drug conjugates (ADCs), where it links antibodies to cytotoxic drugs, enhancing targeted cancer therapy. Additionally, it is employed in the preparation of biosensors, immobilization of enzymes, and the study of protein interactions. Its bifunctional nature makes it a versatile tool in biochemical research and therapeutic development.
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