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Merck

D182257

Sigma-Aldrich

3,5-Dimethyl-1-pyrazolylformaminidium nitrate

97%

Sinónimos:

1-Amidino-3,5-dimethylpyrazole nitrate, 3,5-Dimethylpyrazole-1-carboxamidine nitrate

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About This Item

Fórmula empírica (notación de Hill):
C6H10N4 · HNO3
Número de CAS:
Peso molecular:
201.18
Beilstein/REAXYS Number:
3599170
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

97%

form

powder

mp

167-168 °C (dec.) (lit.)

SMILES string

O[N+]([O-])=O.Cc1cc(C)n(n1)C(N)=N

InChI

1S/C6H10N4.HNO3/c1-4-3-5(2)10(9-4)6(7)8;2-1(3)4/h3H,1-2H3,(H3,7,8);(H,2,3,4)

InChI key

AGYXIUAGBLMBGV-UHFFFAOYSA-N

Application

Guanylating reagent for amines.

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_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Journal of Carbohydrate Chemistry, 12, 1173-1173 (1993)
Orakan Hanpanich et al.
Nucleosides, nucleotides & nucleic acids, 39(1-3), 156-169 (2019-10-15)
The cationic copolymer poly(L-lysine)-graft-dextran (PLL-g-Dex) has nucleic acid chaperone-like activity. The copolymer facilitates both DNA hybridization and strand exchange reactions. For these reasons, DNA-based enzyme (DNAzyme) activity is enhanced in the presence of copolymer. In this study, we evaluated activities
Peter Pogány et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 71(4), 1466-1473 (2008-06-20)
In the paper a joint experimental and theoretical study of 3,5-dimethyl-1H-pyrazole-1-carboxamidine (L) as well as its complexes CoL2(H2O)2(NO3)2 and NiL2(H2O)2(NO3)2 is reported. On the basis of FT-IR experiments and a DFT-derived scaled quantum mechanical force field the normal coordinate analysis
Antonia G Miller et al.
Annals of the New York Academy of Sciences, 1043, 195-200 (2005-07-23)
Protein cross-linking via the Maillard reaction with alpha-dicarbonyl compounds has been the subject of intense scrutiny in the literature. We report here a study of the impact of this cross-linking on enzyme function. Protein function following glycation was examined by
A Bernhardt et al.
The journal of peptide research : official journal of the American Peptide Society, 50(2), 143-152 (1997-08-01)
Peptide-4-nitroanilides can be quickly synthesised using an Fmoc-based approach on 2-chlorotritylchloride resin. Preformed building blocks Fmoc-Xaa-NH-Np (Xaa = Cit, Cys, Gln, His, Lys, Orn, Ser, Thr, Tyr, Trp) can be attached via side chain to the 2-chlorotritylchloride linker of the

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