Product Details:
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Name: | 3-(1-Pyridinio)-1-propanesulfonate | Cas No: | 15471-17-7 |
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Application: | Biochemical Reagents | Purity: | 99% |
Classification: | In Vitro Diagnostic Reagents | Form: | Power |
Color: | White | Samples: | Available |
Package: | 1kg/5kg/25kg | Transport: | Courier/Air/Sea |
High Light: | CAS 15471-17-7 Biochemical Reagent,Biochemical Reagent NDSB 201,99% 3-(1-Pyridinio)-1-Propanesulfonate |
CAS 15471-17-7 Biochemical Reagent NDSB 201 3-(1-Pyridinio)-1-propanesulfonate
Basic information |
Product Name: | 3-(1-Pyridinio)-1-propanesulfonate |
CAS: | 15471-17-7 |
MF: | C8H11NO3S |
MW: | 201.24 |
EINECS: | 239-491-3 |
Mol File: | 15471-17-7.mol |
solubility: | Methanol (Slightly), Water (Slightly) |
Color: | White |
Form: | Power |
Melting point |
275-277 °C |
Fp | 160 °C |
storage temp. | Sealed in dry,Room Temperature |
Usage And Synthesis |
Description: | 3-(1-Pyridinio)-1-propanesulfonate is a white crystalline powder used to prepare electroplating additives.It has good thermal qualitative and chemical stability, and its mechanical strength is also very good. The low polymer molecular weight is prone to disproportionation and cross-linking reactions. |
Uses: | 3-(1-Pyridinio)-1-propanesulfonate is a non detergent sulfobetaine used as a mild solubilizing and stabilizing agent for halophilic malate dehydrogenase, halophilic elongation factor Tu (hTu), pig heart malate dehydrogenase, chicken egg w hite lysozyme and E. coli beta-galactosidase. Preserves the antigenic conformation of serine protease gp76. Does not interfere with colorimetric assays using p-nitrophenylphosphate and o-nitrophenyl -b-D-galactopyranoside as substrates. Reduces aggregation and significantly improves protein renaturation. Zwitterionic over a wide pH range. Does not absorb significantly in the near-UV range. Ca n be easily removed by dialysis. |
Uses: | Stronger leveling agent in nickel electroplating |
Uses: |
As a Bronsted acid ionic liquid catalyst in combination with H2SO4 and H3PO4 for the dehydration of glycerol to acrolein via semi-batch reaction technique. |
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