Tricyclazole
- CAS NO.:41814-78-2
- Empirical Formula: C9H7N3S
- Molecular Weight: 189.24
- MDL number: MFCD00072466
- EINECS: 255-559-5
- SAFETY DATA SHEET (SDS)
- Update Date: 2024-11-19 23:02:33
What is Tricyclazole?
Description
log Kow: 1.4. Solubility: In water at 25 ?C, 1.6 g/L. In acetone 10.4, methanol 25, xylene 2.1 (all in g/l, 25 ?C). Stability: Stable at 52 ?C. Relatively stable to ultraviolet light.
The Uses of Tricyclazole
Tricyclazole is an common active ingredient in several commercial fungicide products used to control rice blast fungus, in transplanted and direct-seeded rice.
What are the applications of Application
Tricyclazol is a common active ingredient in fungicides
Definition
ChEBI: A triazolobenzothiazole that is [1,2,4]triazolo[3,4-b][1,3]benzothiazole which is substituted at position 5 by a methyl group. A fungicide used for the control of rice blast, it is not approved for use within the European Union.
Metabolism
Animals: Rapid and extensive metabolism.
Plants: The principal metabolite is the hydroxymethyl
analog.
Soil/Environment: Kd 4 (loamy sand, pH 6.5, 1.5%
o.m.), 45 (loam, pH 5.7, 3.1% o.m.), 21 (clay loam, pH 7.4,
1.9% o.m.), 22 (silty clay loam, pH 5.7, 4.1% o.m.).
Toxicity evaluation
Mammalian toxicology. Oral: Acute oral LD50
for rats 314, mice 245, dogs >50 mg/kg. Skin and eye:
Acute percutaneous LD50 for rabbits >2000 mg/kg. Slight
eye irritant; nonirritating to skin (rabbits). Inhalation:
LC50 (1 h) for rats 0.146 mg/L air. NOEL: (2 yr) for
rats 9.6 mg/kg b.w.; for mice 6.7 mg/kg b.w.; (1 yr) for
dogs 5 mg/kg b.w.; 3-generation reproduction for rat
3 mg/kg b.w. ADI: 0.03 mg/kg.
Toxicity class: World
Health Organization (WHO) (a.i.) II; U.S. Environmental
Protection Agency (EPA) (formulation) II RC risk Xn
(R22). Ecotoxicology. Birds: Acute oral LD50 for mallard
ducks and bobwhite quail >100 mg/kg. Fish: LC50 for
bluegill sunfish 16.0, rainbow trout 7.3, goldfish fingerlings
13.5 mg/l. Daphnia: LC50 (48 h) > 20 mg/l; NOEC (21 d)
0.96 mg/L.
Properties of Tricyclazole
Melting point: | 187-188°C |
Boiling point: | 275 °C |
Density | 1.2292 (rough estimate) |
refractive index | 1.5500 (estimate) |
storage temp. | Keep in dark place,Inert atmosphere,Room temperature |
solubility | Chloroform (Slightly), DMSO (Slightly), Ethyl Acetate (Very Slightly), Methanol |
pka | 2.40±0.40(Predicted) |
form | neat |
form | Solid |
color | Light yellow to yellow |
Water Solubility | 1.6g/L(25 ºC) |
BRN | 980261 |
InChI | InChI=1S/C9H7N3S/c1-6-3-2-4-7-8(6)12-5-10-11-9(12)13-7/h2-5H,1H3 |
CAS DataBase Reference | 41814-78-2(CAS DataBase Reference) |
NIST Chemistry Reference | Tricyclazole(41814-78-2) |
EPA Substance Registry System | Tricyclazole (41814-78-2) |
Safety information for Tricyclazole
Signal word | Danger |
Pictogram(s) |
Skull and Crossbones Acute Toxicity GHS06 |
GHS Hazard Statements |
H301:Acute toxicity,oral H412:Hazardous to the aquatic environment, long-term hazard |
Precautionary Statement Codes |
P264:Wash hands thoroughly after handling. P264:Wash skin thouroughly after handling. P270:Do not eat, drink or smoke when using this product. P273:Avoid release to the environment. P301+P310:IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician. P405:Store locked up. P501:Dispose of contents/container to..… |
Computed Descriptors for Tricyclazole
InChIKey | DQJCHOQLCLEDLL-UHFFFAOYSA-N |
SMILES | S1C2=CC=CC(C)=C2N2C=NN=C12 |
Abamectin manufacturer
ENTOMIC CHEMICALS
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