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275557

Sigma-Aldrich

1-Ethylguanidine sulfate

98%

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About This Item

Linear Formula:
[C2H5NHC(=NH)NH2]2·H2SO4
CAS Number:
3482-86-8
Molecular Weight:
272.33
EC Number:
222-467-1
MDL number:
MFCD00013130
UNSPSC Code:
12352100
PubChem Substance ID:
24856655
NACRES:
NA.22

Quality Level

100

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.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

275557-5G:
275557-25G:
275557-VAR:
275557-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCP7962
MKCF2140
MKBX3549V
MKBQ9884V
MKBP2518V

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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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