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5 G
$106.00
About This Item
Linear Formula:
[C2H5NHC(=NH)NH2]2·H2SO4
CAS Number:
Molecular Weight:
272.33
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
98%
form
solid
mp
244 °C (dec.) (lit.)
functional group
amine
SMILES string
OS(O)(=O)=O.CCNC(N)=N.CCNC(N)=N
InChI
1S/2C3H9N3.H2O4S/c2*1-2-6-3(4)5;1-5(2,3)4/h2*2H2,1H3,(H4,4,5,6);(H2,1,2,3,4)
InChI key
UKQVDMIAGTYDFN-UHFFFAOYSA-N
Related Categories
Application
1-Ethylguanidine sulfate may be used in chemical synthesis studies.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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O G Busygina et al.
Biokhimiia (Moscow, Russia), 61(1), 119-125 (1996-01-01)
Guanidine thiol derivatives--a new class of soluble guanylate cyclase activators--have been studied. Guanidine thiols contain in their molecule both the guanidine and thiol groups which act as donors acceptors of nitric oxide (NO), respectively. The role of the guanidine thiol
J M Farley et al.
The Journal of physiology, 337, 753-768 (1983-04-01)
The effects of intracellular application of three compounds - QX314, N-ethylguanidine and N-octylguanidine - on the acetylcholine-activated ionic channels in chick myoballs were examined. Voltage-clamped myoballs were internally perfused using the suction-pipette technique. Changes in the internal ionic environment of
S M Vogel et al.
The Journal of general physiology, 83(6), 901-918 (1984-06-01)
Methyl- and ethylguanidine block the endplate current in frog muscle. Both derivatives blocked inward-going endplate currents without affecting outward endplate currents. Repetitive stimulation that evoked several inward endplate currents enhanced the block, which suggests that these agents interact with open
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