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Chemical Structure| 19829-29-9 Chemical Structure| 19829-29-9

Structure of 19829-29-9

Chemical Structure| 19829-29-9

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Product Details of [ 19829-29-9 ]

CAS No. :19829-29-9
Formula : C5H5NS
M.W : 111.16
SMILES Code : S=C1C=CNC=C1
MDL No. :N/A

Safety of [ 19829-29-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H315-H319-H332-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 19829-29-9 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 19829-29-9 ]

[ 19829-29-9 ] Synthesis Path-Downstream   1~18

  • 1
  • [ 19829-29-9 ]
  • [ 5402-20-0 ]
  • [ 2645-22-9 ]
  • 3
  • [ 19829-29-9 ]
  • [ 127-65-1 ]
  • [ 2645-22-9 ]
  • Natrium-S-(4-pyridyl)-N,N'-bis(tosyl)sulfodiimidat [ No CAS ]
  • [ 70-55-3 ]
  • 4
  • [ 19829-29-9 ]
  • [ 30066-82-1 ]
  • [ 98-64-6 ]
  • [ 2645-22-9 ]
  • Natrium-N,N'-bis(p-chlorphenylsulfonyl)-S-(4-pyridyl)sulfodiimidat [ No CAS ]
  • 5
  • [ 19829-29-9 ]
  • [ 29917-03-1 ]
  • [ 2645-22-9 ]
  • [ 1129-26-6 ]
  • Natrium-N,N'-bis(p-methoxyphenylsulfonyl)-S-(4-pyridyl)sulfodiimidat [ No CAS ]
  • 7
  • [ 2645-22-9 ]
  • [ 60-24-2 ]
  • [ 19829-29-9 ]
  • [ 1892-29-1 ]
  • 8
  • [ 2645-22-9 ]
  • Yeast cytochrome c [ No CAS ]
  • [ 19829-29-9 ]
  • 9
  • [ 2645-22-9 ]
  • [ 38170-37-5 ]
  • [ 72-89-9 ]
  • [ 19829-29-9 ]
  • [ 26157-58-4 ]
  • 10
  • [ 2645-22-9 ]
  • [ 38170-37-5 ]
  • [ 317-66-8 ]
  • [ 19829-29-9 ]
  • C8H19N2O(1+) [ No CAS ]
  • 11
  • [ 2645-22-9 ]
  • [ 38170-37-5 ]
  • [ 2140-48-9 ]
  • [ 19829-29-9 ]
  • C9H21N2O(1+) [ No CAS ]
  • 12
  • [ 2645-22-9 ]
  • [ 38170-37-5 ]
  • [ 5060-32-2 ]
  • [ 19829-29-9 ]
  • [ 1242098-01-6 ]
  • 13
  • [ 2645-22-9 ]
  • [ 38170-37-5 ]
  • [ 1763-10-6 ]
  • [ 19829-29-9 ]
  • C21H45N2O(1+) [ No CAS ]
  • 14
  • [ 2645-22-9 ]
  • [ 38170-37-5 ]
  • [ 1264-52-4 ]
  • [ 19829-29-9 ]
  • [ 179617-18-6 ]
  • 15
  • [ 2645-22-9 ]
  • [ 38170-37-5 ]
  • [ 1264-57-9 ]
  • [ 19829-29-9 ]
  • C15H33N2O(1+) [ No CAS ]
  • 16
  • [ 2645-22-9 ]
  • [ 38170-37-5 ]
  • lauroyl coenzyme A [ No CAS ]
  • [ 19829-29-9 ]
  • [ 62570-43-8 ]
  • 17
  • [ 2645-22-9 ]
  • (human serum albumin)-SSH [ No CAS ]
  • [ 19829-29-9 ]
  • conjugate of human serum albumin with 4,4'-dithiodipyridine [ No CAS ]
YieldReaction ConditionsOperation in experiment
Sulfanes in HSA were produced following different procedures, depending on the experiment. For most determinations, mixed HSA disulfides were incubated with equimolar Na2S in phosphate buffer (100 mM, pH 7.4, 0.1 mM DTPA, 25 °C) for a specified period, followed by gel filtration. Persulfides for kinetic studies toward <strong>[2645-22-9]4,4'-dithiodipyridine</strong> (DTDPy) were preparedby incubating 6 muM HSA-SOH with equimolar Na2S in phosphate buffer (100 mM, pH 7.4, 0.1 mM DTPA, 25 °C) during variable periods of time. Persulfides for kinetic studies toward peroxynitrite were prepared by reacting HSA-TNB with Na2S. HSA-SSH was quantified based on the amount of TNB released and purified by gel filtration on Sephadex G-10 equilibrated with phosphate buffer (30 mM, pH 7.4). Solutions were kept under argon and on ice to minimize decay.
  • 18
  • [ 2645-22-9 ]
  • (human serum albumin)-SSO<SUB>3</SUB>H [ No CAS ]
  • [ 19829-29-9 ]
  • conjugate of human serum albumin with 4,4'-dithiodipyridine [ No CAS ]
YieldReaction ConditionsOperation in experiment
Sulfanes in HSA were produced following different procedures, depending on the experiment. For most determinations, mixed HSA disulfides were incubated with equimolar Na2S in phosphate buffer (100 mM, pH 7.4, 0.1 mM DTPA, 25 °C) for a specified period, followed by gel filtration. Persulfides for kinetic studies toward <strong>[2645-22-9]4,4'-dithiodipyridine</strong> (DTDPy) were preparedby incubating 6 muM HSA-SOH with equimolar Na2S in phosphate buffer (100 mM, pH 7.4, 0.1 mM DTPA, 25 °C) during variable periods of time. Persulfides for kinetic studies toward peroxynitrite were prepared by reacting HSA-TNB with Na2S. HSA-SSH was quantified based on the amount of TNB released and purified by gel filtration on Sephadex G-10 equilibrated with phosphate buffer (30 mM, pH 7.4). Solutions were kept under argon and on ice to minimize decay.
 

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