3,5-dimethylpyrazole-1-carboximidamide hydrochloride
Names
[ CAS No. ]:
40027-64-3
[ Name ]:
3,5-dimethylpyrazole-1-carboximidamide hydrochloride
[Synonym ]:
3,5-dimethylpyrazole-1-carboximidamide hydrochloride
3,5-Dimethyl-1-pyrazolylformamidinium hydrochloride
Pyrazole-1-carboxamidine,3,5-dimethyl-,monohydrochloride
3,5-dimethyl-1h-pyrazole-1-carboximidamide hydrochloride(1:1)
3,5-Dimethylpyrazole-1-carboxamidine monohydrochloride
1-amidino-3,5-dimethylpyrazole hydrochloride
3,5-Dimethyl-1-guanylpyrazole hydrochloride
1-Guanyl-3,5-dimethylpyrazole hydrochloride
3,5-dimethyl-1H-pyrazole-1-carboxamidine hydrochloride
Chemical & Physical Properties
[ Molecular Formula ]:
C6H11ClN4
[ Molecular Weight ]:
174.63100
[ Exact Mass ]:
174.06700
[ PSA ]:
67.69000
[ LogP ]:
1.84350
MSDS
Toxicological Information
CHEMICAL IDENTIFICATION
- RTECS NUMBER :
- UQ6379500
- CHEMICAL NAME :
- Pyrazole-1-carboxamidine, 3,5-dimethyl-, monohydrochloride
- CAS REGISTRY NUMBER :
- 40027-64-3
- LAST UPDATED :
- 198702
- DATA ITEMS CITED :
- 1
- MOLECULAR FORMULA :
- C6-H10-N4.Cl-H
- MOLECULAR WEIGHT :
- 174.66
- WISWESSER LINE NOTATION :
- T5NNJ AYZUM C1 E1 &GH
HEALTH HAZARD DATA
ACUTE TOXICITY DATA
- TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Intraperitoneal
- SPECIES OBSERVED :
- Rodent - mouse
- DOSE/DURATION :
- 160 mg/kg
- TOXIC EFFECTS :
- Behavioral - excitement
- REFERENCE :
- AITEAT Archivum Immunologiae et Therapiae Experimentalis. (Ars Polona, POB 1001, 00-068 Warsaw 1, Poland) V.10- 1962- Volume(issue)/page/year: 22,813,1974
Safety Information
[ Hazard Codes ]:
Xi
[ Risk Phrases ]:
43
[ Safety Phrases ]:
36/37-24/25-22
[ RIDADR ]:
NONH for all modes of transport
[ HS Code ]:
2933199090
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2933199090
[ Summary ]:
2933199090. other compounds containing an unfused pyrazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
Articles
J. Pept. Res. 50(2) , 143-52, (1997)
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,...
Assessment of protein function following cross-linking by alpha-dicarbonyls.Ann. N. Y. Acad. Sci. 1043 , 195-200, (2005)
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 o...
FT-IR and theoretical study of 3,5-dimethyl-1H-pyrazole-1-carboxamidine (L) and the complexes CoL2(H2O)2(NO3)2, NiL2(H2O)2(NO3)2.Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 71(4) , 1466-73, (2008)
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-I...