375144
2-Isopropyl-6-methyl-4-pyrimidinol
99%
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About This Item
Empirical Formula (Hill Notation):
C8H12N2O
CAS Number:
Molecular Weight:
152.19
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
220-561-7
MDL number:
Product Name
2-Isopropyl-6-methyl-4-pyrimidinol, 99%
InChI key
AJPIUNPJBFBUKK-UHFFFAOYSA-N
InChI
1S/C8H12N2O/c1-5(2)8-9-6(3)4-7(11)10-8/h4-5H,1-3H3,(H,9,10,11)
SMILES string
CC(C)c1nc(C)cc(O)n1
assay
99%
mp
172-175 °C (lit.)
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General description
2-Isopropyl-6-methyl-4-pyrimidinol is a pyrimidine compound. It is reported as an major metabolite of pesticide diazinon., It has been identified as urinary metabolite in the general population exposed to organophosphorus compounds (insecticides, flame retardants and plasticizers) and moth repellents used in Japanese households. Photocatalytic oxidation of 2-isopropyl-6-methyl-4-pyrimidinol has been reported.
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 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Bandgap modulation of TiO2 and its effect on the activity in photocatalytic oxidation of 2-isopropyl-6-methyl-4-pyrimidinol.
Lee H-S, et al.
Topics in Catalysis, 35(3-4), 255-260 (2005)
Toshiaki Yoshida et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 880(1), 66-73 (2011-12-02)
An analytical method was developed for simultaneous measurement of urinary metabolites in the general population exposed to organophosphorus compounds (insecticides, flame retardants and plasticizers) and moth repellents used in Japanese households. Fifteen metabolites, dimethylphosphate, dimethylthiophosphate, diethylphosphate, diethylthiophosphate, di-n-butylphosphate, diphenylphosphate, bis(2-ethylhexyl)phosphate
Peter P Egeghy et al.
International journal of environmental research and public health, 8(5), 1727-1754 (2011-06-10)
Children are exposed to a wide variety of pesticides originating from both outdoor and indoor sources. Several studies were conducted or funded by the EPA over the past decade to investigate children's exposure to organophosphate and pyrethroid pesticides and the
Jesús M Marín-Benito et al.
The Science of the total environment, 476-477, 611-621 (2014-02-06)
Dissipation kinetics of pesticides belonging to three chemical groups (linuron, diazinon and myclobutanil) was studied in an unamended agricultural soil and in this soil amended with three organic residues: sewage sludge (SS), grape marc (GM) and spent mushroom substrate (SMS).
Andreas Kretschmann et al.
Environmental toxicology and chemistry, 31(9), 2014-2022 (2012-06-02)
A mechanistic toxicokinetic and toxicodynamic model for acute toxic effects (immobilization, mortality) of the organothiophosphate insecticide diazinon in Daphnia magna is presented. The model was parameterized using measured external and internal (whole-body) concentrations of diazinon, its toxic metabolite diazoxon, and
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