Molecular Formula | C16H19N2NaO9S |
Molar Mass | 438.38 |
Melting Point | >270°C (dec.) |
Water Solubility | Soluble in water (2.5 mg/ml) and dimethyl formamide. |
Solubility | soluble in water (2.5 mg/ml) and DMF |
Appearance | powder |
Color | white to light brown |
Storage Condition | Inert atmosphere,Store in freezer, under -20°C |
Stability | Moisture Sensitive |
MDL | MFCD00054978 |
Use | A sulfhydryl- and amine-reactive crosslinker. |
In vitro study | The crosslinker Sulfo-SMCC consists of a maleimide and an N-hydroxysuccinimide ester group to bind to sulfhydryl groups and primary amines, respectively. Sulfo-SMCC inhibits the end-to-end annealing of stabilized Microtubules (MTs). MTs are treated with 250 μM Sulfo-SMCC, and imaged after incubation for 0 h, 6 h, and 24 h. MTs treated with Sulfo-SMCC shows a constant mean length, independent of the incubation time. |
Hazard Symbols | Xi - Irritant |
Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin. R20/21 - Harmful by inhalation and in contact with skin. R61 - May cause harm to the unborn child |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) S53 - Avoid exposure - obtain special instructions before use. |
WGK Germany | 3 |
HS Code | 29251900 |
Reference Show more | 1. [IF=15.84] Han Yang et al."A Novel Targeted and High‐Efficiency Nanosystem for Combinational Therapy for Alzheimer's Disease."Adv Sci. 2020 Oct;7(19):1902906 |
biological activity | Sulfo-SMCC sodium is a commonly used heterobifunctional crosslinking agent, which is a non-degradable ADC linker, it carries N-hydroxysuccinimide (NHS) Ester and maleimide groups that react with primary amines and sulfhydryl groups, respectively. |
Use | a water-soluble, difunctional crosslinking reagent that combines amine and thiol reactivity into an expanded spacer, typically, coupling to molecules containing primary amines via amide bonds in pH 6.5 buffer (8.5-6.5) and via thioether linkages in pH 7.0 buffer (-), secondary coupling to a particular molecule containing a free thiol group; An Immunoconjugate for the preparation of an enzyme and a hapten carrier molecule conjugate comprising a 9-atom linkage; an expanded fatty spacer that provides stable preferential coupling |