N-Hydroxysulfosuccinimide sodium
Names
[ CAS No. ]:
106627-54-7
[ Name ]:
N-Hydroxysulfosuccinimide sodium
[Synonym ]:
3-Pyrrolidinesulfonic acid, 1-hydroxy-2,5-dioxo-, sodium salt (1:1)
Sodium 1-hydroxy-2,5-dioxopyrrolidine-3-sulfonate
Hydroxy-2,5-dioxopyrrolidine-3-sulfonicacid sodium salt
N-Hydroxysulfosuccinimide sodiumsalt
Sodium 1-hydroxy-2,5-dioxo-3-pyrrolidinesulfonate
sodium,1-hydroxy-2,5-dioxopyrrolidine-3-sulfonate
N-Hydroxysulfosuccinimide Sodium Salt
MFCD00217065
Biological Activity
[Description]:
[Related Catalog]:
[Target]
Non-cleavable
[In Vitro]
[References]
Chemical & Physical Properties
[ Melting Point ]:
250 °C (dec.)(lit.)
[ Molecular Formula ]:
C4H4NNaO6S
[ Molecular Weight ]:
217.132
[ Exact Mass ]:
216.965698
[ PSA ]:
123.19000
[ Storage condition ]:
0-6°C
MSDS
Safety Information
[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S26-S36/37/39
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2925190090
Customs
[ HS Code ]: 2925190090
[ Summary ]:
2925190090 other imides and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%
Articles
J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 968 , 105-11, (2014)
SIRT6 is a histone deacetylase that has been proposed as a potential therapeutic target for metabolic disorders and the prevention of age-associated diseases. Thus the identification of compounds that...
Pd-Ir Core-Shell Nanocubes: A Type of Highly Efficient and Versatile Peroxidase Mimic.ACS Nano 9 , 9994-10004, (2015)
Peroxidase mimics with dimensions on the nanoscale have received great interest as emerging artificial enzymes for biomedicine and environmental protection. While a variety of peroxidase mimics have b...
Interprotein Coupling Enhances the Electrocatalytic Efficiency of Tobacco Peroxidase Immobilized at a Graphite Electrode.Anal. Chem. 87 , 10807-14, (2015)
Covalent immobilization of enzymes at electrodes via amide bond formation is usually carried out by a two-step protocol, in which surface carboxylic groups are first activated with the corresponding c...