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Merck
CN

382213

1-Octylguanidine hemisulfate

97%

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About This Item

Linear Formula:
CH3(CH2)7NHC(=NH)NH2 · 1/2H2SO4
CAS Number:
Molecular Weight:
220.32
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
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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)

SMILES string

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

InChI key

DTTVLDRWEFQROK-UHFFFAOYSA-N

assay

97%

General description

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

pictograms

Exclamation mark

signalword

Warning

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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Studies on nitrogen metabolism in tobacco plants IX. Effect of various compounds on proline biosynthesis in the green leaves.
Noguchi M, et al.
Plant & Cell Physiology, 9(1), 35-47 (1968)
J R de Weille et al.
Brain research, 445(1), 1-11 (1988-03-29)
Kinetics of pyrethroid-modified sodium channels and the interaction of N-octylguanidine with the modified channels have been studied with internally perfused and voltage-clamped squid giant axons. The pyrethroids used were 1R-cis-phenothrin; 1R-cis-permethrin; 1R-cis-cyphenothrin; and 1R-cis-deltamethrin. Modification of sodium channels by pyrethroids
Victoriano Pérez-Vázquez et al.
Journal of bioenergetics and biomembranes, 35(3), 231-241 (2003-09-19)
The yeast mitochondrial unspecific channel (YMUC) sensitivity to inorganic (Ca2+ or Mg2+) or organic (hexyl or octyl-guanidine) cations was measured. The rate of oxygen consumption in State 3 and State 4, the transmembrane potential (deltapsi), mitochondrial swelling, and the polyethylene-glycol
Natalia Pavón et al.
Journal of biochemistry, 149(2), 211-217 (2010-11-30)
Mercurials are known to induce morphological and functional modifications in kidney. The protective effect of octylguanidine on the injury induced by Hg(2+) on renal functions was studied. Octylguanidine administered at a dose of 10 mg/kg body weight prevented the damage
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

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