276669
1,1-Dimethylguanidine sulfate salt
97%
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
[(CH3)2NC(NH2)=NH]2 · H2SO4
CAS Number:
Molecular Weight:
272.33
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-946-0
Beilstein/REAXYS Number:
3916505
MDL number:
Assay:
97%
Form:
powder
InChI key
QSCHFHVDZCPIKX-UHFFFAOYSA-N
InChI
1S/2C3H9N3.H2O4S/c2*1-6(2)3(4)5;1-5(2,3)4/h2*1-2H3,(H3,4,5);(H2,1,2,3,4)
SMILES string
OS(O)(=O)=O.CN(C)C(N)=N.CN(C)C(N)=N
assay
97%
form
powder
mp
300 °C (dec.) (lit.)
functional group
amine
Application
1,1-Dimethylguanidine sulfate salt has been employed:
- as peroxide activator for bleaching cellulosic textiles
- in the synthesis of N2,N2-dimethyl-4-(1-methyl-1H-indol-3-yl)pyrimidine-2,5-diamine, substrate for the modified Pictet-Spengler reaction
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
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Guanidine derivatives used as peroxide activators for bleaching cellulosic textiles.
Cai JY and Evans DJ.
Coloration Technology, 123(2), 115-118 (2007)
Piyush Kumar Agarwal et al.
Beilstein journal of organic chemistry, 8, 1901-1908 (2012-12-05)
A mild, efficient and versatile method has been developed for the construction of a functionalized natural product, meridianin, and its post conversion to pyrimido-β-carboline by cationic π- cyclization. The strategy involves the introduction of an amino group at the C-5
W Zhang et al.
Acta physiologica Scandinavica, 159(1), 1-6 (1997-01-01)
1,1-dimethylguanidine (DMG) is an endogenous nitric oxide (NO) synthesis inhibitor. This study investigates the effects of exogenous DMG administration, in anaesthetized spontaneously hypertensive rats (SHR) and Wistar-Kyoto rats (WKY). Mean blood pressure (MBP), heart rate (HR) and renal sympathetic nerve
J A Hirsch
The Journal of pharmacology and experimental therapeutics, 230(3), 710-717 (1984-09-01)
The effect of guanidine alkyl derivatives on the evoked release of [3H]norepinephrine [( 3H]NE) from spleen strips was examined. Guanidine, methyl guanidine and N,N-dimethyl guanidine all enhanced the field-stimulated release of [3H]NE 2- to 3-fold, whereas N,N'-dimethyl guanidine and propyl
E Benoit
Receptors & channels, 1(3), 181-191 (1993-01-01)
The effects of guanidine and dimethyl guanidine were studied on current- and voltage-clamped nodes of Ranvier, to determine the electrophysiological basis for the guanidine-induced increase in neurotransmitter release. When added to the external solution, guanidine produced positive shifts of K
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