Skip to Content
Merck
All Photos(1)

Key Documents

382213

Sigma-Aldrich

1-Octylguanidine hemisulfate

97%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3(CH2)7NHC(=NH)NH2 · 1/2H2SO4
CAS Number:
Molecular Weight:
220.32
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

SMILES string

OS(O)(=O)=O.CCCCCCCCNC(N)=N.CCCCCCCCNC(N)=N

InChI

1S/2C9H21N3.H2O4S/c2*1-2-3-4-5-6-7-8-12-9(10)11;1-5(2,3)4/h2*2-8H2,1H3,(H4,10,11,12);(H2,1,2,3,4)

InChI key

DTTVLDRWEFQROK-UHFFFAOYSA-N

General description

1-Octylguanidine hemisulfate is a guanidine derivative. Octyl guanidine sulfate is prepared from S-methylisothiourea sulfate and octylamine.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard 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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

G Beaty et al.
Acta physiologica et pharmacologica latinoamericana : organo de la Asociacion Latinoamericana de Ciencias Fisiologicas y de la Asociacion Latinoamericana de Farmacologia, 36(3), 217-232 (1986-01-01)
We have studied the inhibitory effects of several cations (OG+, Mg2+, Ca2+, Sr2+, Ba2+, Mn2+, La3+) on the uniport and exchange pathways for Na+ and K+ of rat liver mitochondria. Swelling of mitochondria suspended in sodium or potassium acetates indicates
G G Re et al.
Bollettino della Societa italiana di biologia sperimentale, 56(6), 625-629 (1980-03-30)
The effects of octylguanidine on the mechanical activity of Guinea-pig heart were investigated. The negative inotropic effect took place in a biphasic manner with a first fast contraction decline process followed, after a temporaneous steady state, by a second slower
Y M Galante et al.
Biochemistry, 21(4), 680-687 (1982-02-16)
The methyl 4-azidobenzimidate derivative of the naturally occurring ATPase inhibitor protein (IF1) of mitochondria binds to the beta subunits of soluble F1-ATPase upon photoactivation [Klein, G., Satre, M., Dianoux, A.-C., & Vignais, P. V. (1981) Biochemistry 20, 1339--1344]. A number
G G Re et al.
Bollettino della Societa italiana di biologia sperimentale, 56(6), 619-624 (1980-03-30)
The effects of octylguanidine on electrical activity of Guinea-pig heart were investigated. The substance (2.7 x 10(-4)M) initially reduced the rate of rise of the action potential without a concomitant modification of the other action potential without a concomitant modification
Elías Parra et al.
Molecular and cellular biochemistry, 269(1-2), 19-26 (2005-03-25)
This study shows that the hydrophobic cation octylguanidine protects against myocardial damage induced by ischemia-reperfusion. The protective effect of the amine was analyzed after 5 min of coronary occlusion followed by 5 min reperfusion in rat hearts. ECG tracings from

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service