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
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 4,5,6,7-Tetrahydrobenzo[d]isoxazole-3-carbaldehyde
  • 1-[6-(1H-1,2,4-triazol-1-yl)pyridin-3-yl]cyclopropan-1-ol
  • tert-Butyl-DL-alanine
  • 4-amino-N-[2-tert-butyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-benzimidazol-5-yl]-N-ethylbenzenesulfonamide