N-Hydroxysulfosuccinimide sodium

Suppliers

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

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

The identification of a novel SIRT6 modulator from Trigonella foenum-graecum using ligand fishing with protein coated magnetic beads.

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...


More Articles


Related Compounds

  • N-hydroxysulfosuccinimide sodium salt hydrate
  • DOTA N-hydroxysulfosuccinimide ester
  • biotinyl-N-hydroxysulfosuccinimide ester
  • m-maleimidobenzoyl-N-hydroxysulfosuccinimide ester
  • iopanoic acid N-hydroxysulfosuccinimide ester
  • 15N1-sodium azide
  • (Z)-1-(3-Ethyl-4-(hydroxymethyl)phenyl)ethanone-O-(4-cyclohexyl-3-(trifluoromethyl)benzyl) Oxime
  • (3aR,6aR)-hexahydro-2H-cyclopenta[d][1,3]oxazol-2-one
  • 2-(6-Cyano-3,4-dihydro-1H-2-benzopyran-1-yl)ethyl methanesulfonate
  • 1-(2-Oxoethyl)-3,4-dihydro-1H-2-benzopyran-6-carbonitrile
  • 2,3-Dibromo-5,6-dichloropyridine
  • 2-(2,3,4-Trihydroxyphenyl)acetaldehyde
  • (1S)-1-(4-chloropyridin-2-yl)-2,2,2-trifluoroethan-1-ol
  • (1R)-1-(4-chloropyridin-2-yl)-2,2,2-trifluoroethan-1-ol
  • 5-Bromo-alpha-(trifluoromethyl)pyridine-2-methanol
  • (1R)-1-(5-bromo-3-pyridyl)-2,2,2-trifluoro-ethanol
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.