Hydroxyguanidine Sulfate

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Names

[ CAS No. ]:
6345-29-5

[ Name ]:
Hydroxyguanidine Sulfate

[Synonym ]:
hydroxyguanidine sulfate

Chemical & Physical Properties

[ Density]:
1.73 g/cm3

[ Boiling Point ]:
306.8ºC at 760 mmHg

[ Melting Point ]:
132-134ºC dec.

[ Molecular Formula ]:
C2H12N6O6S

[ Molecular Weight ]:
248.21800

[ Flash Point ]:
139.4ºC

[ Exact Mass ]:
248.05400

[ PSA ]:
247.24000

[ LogP ]:
0.52720

[ Index of Refraction ]:
1.602

[ Storage condition ]:
2-8°C

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
26-36/37/39-27

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2925290090

Precursor & DownStream

Precursor

DownStream

  • 1,2,4-Oxadiazol-3-amine,5-(2-piperazinyl)-(9CI)
  • 3-(3-amino-1,2,4-oxadiazole-5-yl)-quinuclidine
  • (methanehydrazonoylamino) hydrogen sulfate

Customs

[ HS Code ]: 2925290090

[ Summary ]:
2925290090 other imines and their derivatives; salts thereof。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%

Articles

A new class of NO-donor pro-drugs triggered by γ-glutamyl transpeptidase with potential for reno-selective vasodilatation.

Chem. Commun. (Camb.) 49(14) , 1389-91, (2013)

This communication describes the synthesis of a new class of N-hydroxyguanidine (NHG) pro-drugs which release nitric oxide (NO), triggered by the action of γ-glutamyl transpeptidase (γ-GT), and have p...

Microsomal formation of nitric oxide and cyanamides from non-physiological N-hydroxyguanidines: N-hydroxydebrisoquine as a model substrate.

Biochem. Pharmacol. 58(3) , 439-45, (1999)

The microsomal oxidative transformation of a non-physiological N-hydroxyguanidine was demonstrated for the first time for N-hydroxydebrisoquine as a model substrate (Clement et al., Biochem Pharmacol ...

Unusual oxidative chemistry of N(omega)-hydroxyarginine and N-hydroxyguanidine catalyzed at an engineered cavity in a heme peroxidase.

J. Biol. Chem. 275(12) , 8582-91, (2000)

Heme enzymes are capable of catalyzing a range of oxidative chemistry with high specificity, depending on the surrounding protein environment. We describe here a reaction catalyzed by a mutant of cyto...


More Articles


Related Compounds

  • Penbutolol sulfate
  • methyl sulfate,trimethyl-[3-[[(Z)-octadec-9-enoyl]amino]propyl]azanium
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  • {[5-(Difluoromethyl)-1,2-oxazol-3-yl]methyl}(methyl)amine hydrochloride
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  • [2-Fluoro-3-(thiophen-2-yl)propyl](methyl)amine hydrochloride
  • 2-fluoro-3-(1H-indol-3-yl)propan-1-amine hydrochloride
  • [2-fluoro-3-(1H-indol-3-yl)propyl](methyl)amine hydrochloride
  • 2-fluoro-3-(1-methyl-1H-indol-3-yl)propan-1-amine hydrochloride
  • 2-fluoro-3-(1-methyl-1H-pyrazol-4-yl)propan-1-amine dihydrochloride
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