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About This Item
Linear Formula:
[NH2C(=NH)NH2]2 · H2SO4
CAS Number:
Molecular Weight:
108.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-826-8
Beilstein/REAXYS Number:
3632154
MDL number:
Product Name
Guanidine sulfate salt, 99%
InChI key
UYAKTBUPMOOXNW-UHFFFAOYSA-N
InChI
1S/2CH5N3.H2O4S/c2*2-1(3)4;1-5(2,3)4/h2*(H5,2,3,4);(H2,1,2,3,4)
SMILES string
NC(N)=N.NC(N)=N.OS(O)(=O)=O
assay
99%
form
powder
mp
290-293 °C (dec.) (lit.)
functional group
amine
Quality Level
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General description
The multicomponent condensation of guanidine sulfate salt with H2S and CH2O was studied.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Multicomponent reactions of urea and its derivatives with CH2O and H2S in the synthesis of 1, 3, 5-thiadiazinane-4-(thi) ones and macroheterocycles.
ARKIVOC (Gainesville, FL, United States), 8, 149-162 (2011)
J-K Ryu et al.
Andrology, 1(2), 216-222 (2013-01-15)
A prerequisite for the successful clinical application of gene therapy in erectile dysfunction (ED) is the availability of safe and efficient gene delivery systems. The aim of this study was to examine the effectiveness of guanidinylated bioreducible polymer (GBP) polyplexes
Neelesh Singh et al.
Applied biochemistry and biotechnology, 169(8), 2315-2325 (2013-03-01)
Physiologically as well as industrially, α-galactosidases are very important enzymes, but very little is known about the stability and folding aspect of enzyme. In the present study, we have investigated the temperature, pH, and guanidine hydrochloride (GuHCl) induced unfolding of
Yoganjaneyulu Kasetti et al.
Journal of molecular modeling, 19(4), 1865-1874 (2013-01-18)
Several therapeutically important compounds contain guanylurea (GU) moiety. The appropriate tautomeric state of these species has not been explored, preliminary studies indicated that the traditional representation of this class of compounds use a high energy tautomeric state. In this work
Philipp Selig et al.
Chemical communications (Cambridge, England), 49(28), 2930-2932 (2013-03-06)
The first synthesis of highly substituted 3-alkyl-oxetan-2-ylidenes from allenoates was developed by using the bicyclic guanidine 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD) as an exceptionally active nitrogen Lewis base catalyst.
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