N,N'-Ethylenebis(iodoacetamide)

95%

Reagent Code: #218880
fingerprint
CAS Number 7250-43-3

science Other reagents with same CAS 7250-43-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 395.96 g/mol
Formula C₆H₁₀I₂N₂O₂
badge Registry Numbers
MDL Number MFCD00728185
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a crosslinking agent in molecular biology for modifying proteins and nucleic acids. It reacts selectively with thiol groups (-SH) in cysteine residues, enabling the formation of covalent crosslinks between biomolecules. Commonly applied in protein footprinting, enzyme active site labeling, and stabilizing protein-protein interactions. Also utilized in bioconjugation techniques for attaching labels or immobilizing biomolecules on surfaces. Its bifunctional iodoacetamide groups ensure specific and stable alkylation, making it valuable in structural studies and biochemical assays.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿4,180.00
inventory 25mg
10-20 days ฿10,170.00
N,N'-Ethylenebis(iodoacetamide)
No image available

Used as a crosslinking agent in molecular biology for modifying proteins and nucleic acids. It reacts selectively with thiol groups (-SH) in cysteine residues, enabling the formation of covalent crosslinks between biomolecules. Commonly applied in protein footprinting, enzyme active site labeling, and stabilizing protein-protein interactions. Also utilized in bioconjugation techniques for attaching labels or immobilizing biomolecules on surfaces. Its bifunctional iodoacetamide groups ensure specific and

Used as a crosslinking agent in molecular biology for modifying proteins and nucleic acids. It reacts selectively with thiol groups (-SH) in cysteine residues, enabling the formation of covalent crosslinks between biomolecules. Commonly applied in protein footprinting, enzyme active site labeling, and stabilizing protein-protein interactions. Also utilized in bioconjugation techniques for attaching labels or immobilizing biomolecules on surfaces. Its bifunctional iodoacetamide groups ensure specific and stable alkylation, making it valuable in structural studies and biochemical assays.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...