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375144

Sigma-Aldrich

2-Isopropyl-6-methyl-4-pyrimidinol

99%

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About This Item

Empirical Formula (Hill Notation):
C8H12N2O
CAS Number:
2814-20-2
Molecular Weight:
152.19
EC Number:
220-561-7
MDL number:
MFCD00044811
UNSPSC Code:
12352100
PubChem Substance ID:
24863367
NACRES:
NA.22

assay

99%

mp

172-175 °C (lit.)

SMILES string

CC(C)c1nc(C)cc(O)n1

InChI

1S/C8H12N2O/c1-5(2)8-9-6(3)4-7(11)10-8/h4-5H,1-3H3,(H,9,10,11)

InChI key

AJPIUNPJBFBUKK-UHFFFAOYSA-N

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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.[1],[2] 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.[3] Photocatalytic oxidation of 2-isopropyl-6-methyl-4-pyrimidinol has been reported.[4]

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_germany

WGK 2

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
05310HY

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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
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).
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
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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