Basic information Safety Supplier Related

1,3,5-Trimethylpyrazole

Basic information Safety Supplier Related

1,3,5-Trimethylpyrazole Basic information

Product Name:
1,3,5-Trimethylpyrazole
Synonyms:
  • 1,3,5-Trimethylpyrazole ,98%
  • 1,3,5,-Trimethylpyrazole,99%
  • 1,3,5-TriMethylpyrazole, 97+%
  • 1,3,5-Trimethyl-1H-pyrazole98%
  • VITAS-BB TBB000655
  • 1H-Pyrazole, 1,3,5-trimethyl-
  • Pyrazole, 1,3,5-trimethyl-
  • 1,3,5-TRIMETHYL-1H-PYRAZOLE
CAS:
1072-91-9
MF:
C6H10N2
MW:
110.16
EINECS:
626-960-6
Product Categories:
  • Pyrazoles
  • Nucleotides and Nucleosides
  • Bases & Related Reagents
  • Nucleotides
  • Pyrazoles & Triazoles
  • Building Blocks
  • Heterocyclic Building Blocks
  • Pyrazoles & Triazoles
Mol File:
1072-91-9.mol
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1,3,5-Trimethylpyrazole Chemical Properties

Melting point:
38-41 °C (lit.)
Boiling point:
168-170 °C
Density 
0.93
refractive index 
1.4589
Flash point:
93 °F
storage temp. 
Sealed in dry,Room Temperature
solubility 
soluble in Methanol
form 
powder to lump to clear liquid
pka
3.30±0.10(Predicted)
color 
White or Colorless to Light yellow
λmax
220nm(MeOH)(lit.)
BRN 
110515
InChI
InChI=1S/C6H10N2/c1-5-4-6(2)8(3)7-5/h4H,1-3H3
InChIKey
HNOQAFMOBRWDKQ-UHFFFAOYSA-N
SMILES
N1(C)C(C)=CC(C)=N1
CAS DataBase Reference
1072-91-9(CAS DataBase Reference)
NIST Chemistry Reference
1,3,5-Trimethylpyrazole(1072-91-9)
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Safety Information

Hazard Codes 
Xi,F
Risk Statements 
10-36/37/38
Safety Statements 
16-26-36
RIDADR 
UN 1325 4.1/PG 3
WGK Germany 
3
Hazard Note 
Flammable
HazardClass 
3
PackingGroup 
III
HS Code 
29331990

MSDS

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1,3,5-Trimethylpyrazole Usage And Synthesis

Chemical Properties

White Low-Mekting Solid

Uses

1,3,5-Trimethylpyrazole is a compound used for chemical synthesis[1].

Definition

ChEBI: 1,3,5-Trimethyl-1H-pyrazole is a member of pyrazoles.

Synthesis Reference(s)

Canadian Journal of Chemistry, 71, p. 410, 1993 DOI: 10.1139/v93-060

References

[1] Li QB, et al. Design, Synthesis, and Biological Activities of Novel 1,3,5-Trimethylpyrazole-Containing Malonamide Derivatives. Molecules. 2019 Feb 3;24(3). DOI:10.3390/molecules24030562

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