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Merck
CN

D182257

3,5-Dimethyl-1-pyrazolylformaminidium nitrate

97%

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C6H10N4 · HNO3
CAS Number:
38184-47-3
Molecular Weight:
201.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24893552
EC Number:
253-815-0
Beilstein/REAXYS Number:
3599170
MDL number:
MFCD00012715

Key Documents

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Product Name

3,5-Dimethyl-1-pyrazolylformaminidium nitrate, 97%

InChI key

AGYXIUAGBLMBGV-UHFFFAOYSA-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)

SMILES string

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

assay

97%

form

powder

mp

167-168 °C (dec.) (lit.)

Quality Level

200

Related Categories

Application

Guanylating reagent for amines.

pictograms

Exclamation mark
GHS07

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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Certificates of Analysis (COA)

Lot/Batch Number
BCBB1318
BCBB1318V
040456/1
08201LE
05401LE

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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
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
L Spero et al.
Biochimica et biophysica acta, 251(3), 345-356 (1971-12-28)
Guanidination of the free amino groups of staphylococcal enterotoxin B with 3,5-dimethyl-1-guanylpyrazole converted 31-32 of 33 epsilon-amino groups and 30% of the N-terminal residue. This product, although markedly reduced in solubility, suffered no gross change in conformation and retained full
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