275557
1-Ethylguanidine sulfate
98%
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About This Item
Linear Formula:
[C2H5NHC(=NH)NH2]2·H2SO4
CAS Number:
Molecular Weight:
272.33
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
222-467-1
MDL number:
Product Name
1-Ethylguanidine sulfate, 98%
InChI key
UKQVDMIAGTYDFN-UHFFFAOYSA-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)
SMILES string
OS(O)(=O)=O.CCNC(N)=N.CCNC(N)=N
assay
98%
form
solid
mp
244 °C (dec.) (lit.)
functional group
amine
Quality Level
Related Categories
Application
1-Ethylguanidine sulfate may be used in chemical synthesis studies.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
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
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
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
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