N-Hydroxysulfosuccinimide sodium salt is a water-soluble sulfonated analog of N-hydroxysuccinimide. It can undergo a coupling reaction with carboxylic acids in the presence of carbodiimides such as 1-ethyl-3-(3-dimethylamin opropyl)carbodiimide(EDC) to form hydrophilic N-hydroxysulfosuccinimide active esters. These esters are useful in protein.
Synonym: 1-(Benzoyloxy)-2,5-dioxo-3-pyrrolidinesulfonic acid sodium salt, Benzoic acid (3-sulfo-N-succinimidyl) ester sodium salt, Benzoic acid N-hydroxysulfosuccinimide ester sodium salt.TIANFUCHEM--106627-54-7--N-Hydroxysulfosuccinimide sodium salt factory price Our company was built in 2009 with an ISO certificate.In the past 10 years, we have grown up as a famous fine chemicals supplier in China And we had established s.Sodium and Potassium chlorate synthesis, the complete guide Made by Plante1999 It is know that chlorates can be easily made. Much of the chlorate made by individual are used in pyrotechnic, but this thread will be mostly intended to use the chlorate as a general oxidizer in the laboratory. It is also know that there is many way to make.
N-Hydroxysulfosuccinimide sodium salt (Sulfo-NHS) is used in conjunction with EDC-HCl (CovaChem 13503). Sulfo-NHS is used as a catalyst in the zero-length crosslinking of proteins with EDC. Sulfo-NHS functions by stabilizing the protein-EDC intermediate, thus allowing for a more efficient crosslinking reaction. Package Sizes: 500 mg, 1 gram, 5.
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Sulfo-NHS (N-hydroxysulfosuccinimide) enables control and modification of carbodiimide crosslinking reactions involving activation of carboxylates (—COOH) for conjugation with primary amines (—NH2). Derivatives are easily synthesized by mixing the Sulfo-NHS with a carboxyl-containing molecule and a dehydrating agent such as the carbodiimide.
The N-Hydroxysulfosuccinimide sodium salt with the cas number 106627-54-7, is also called sodium 1-hydroxy-2,5-dioxopyrrolidine-3-sulfonate named by IUPAC.
Structure, properties, spectra, suppliers and links for: N-hydroxysulfosuccinimide.
Supplementary info Synthesis of tetraoctylammonium linoleate (N8888 C18:2) Sodium hydroxide (0.71g, 17.8mmol) was added to linoleic acid (5.55ml, 17.8mmol) dissolved in ethanol 70% (50mL). The reaction mixture was stirred overnight at room temperature. Sodium linoleate (5.4g) was obtained as a white soap after removal of the solvent under.
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An efficient method for synthesis of sulphacetamide sodium by ultrasonic irradiation at room temperature is described. Quality of product prepared by this method has been found to be comparable with standard methods using refluxing conditions. Keywords: Sulphacetamide sodium, Ultrasonic irradiation Introduction Sulphacetamide sodium 1 (sodium.
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Find manufacturers and suppliers for N-Hydroxysulfosuccinimide sodium salt, 106627-54-7. Synonyms: NHSS; Sodium 1-hydroxy-2,5-dioxo-pyrrolidine-3-sulfonate; sodium 1-hydroxy-2,5-dioxo-3-pyrrolidinesulfonate.
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Essay Lab Report On Electrochemical Impedance Spectroscopy. followed by the activation carboxylate groups on Si and Au electrode in 75mM N-(3-(Dimethylamino)propyl-N’-(ethylcarbodiimide hydrochloride) and 15mM N-hydroxysulfosuccinimide sodium salt in 50mM buffer solution for about 1h.