Myclobutanil

Myclobutanil
Names
IUPAC name
2-(4-Chlorophenyl)-2-(1,2,4-triazol-1-ylmethyl)hexanenitrile
Identifiers
88671-89-0 YesY
3D model (Jmol) Interactive image
7138849
ChEBI CHEBI:75281 N
ChemSpider 6096 N
9252226 (2R) YesY
ECHA InfoCard 100.115.883
EC Number 410-400-0
KEGG C18477 YesY
MeSH Systhane
PubChem 6336
11077077 (2R)
38989055 (2S)
RTECS number XZ5257000
UN number 3077
Properties
C15H17ClN4
Molar mass 288.78 g·mol−1
Appearance Pale, yellow, translucent crystals
Melting point 63 to 68 °C (145 to 154 °F; 336 to 341 K)
Boiling point 202 to 208 °C (396 to 406 °F; 475 to 481 K) at 130 Pa
142 mg dm−3
Hazards
GHS pictograms
GHS signal word Warning
H302, H319, H361, H411
P273, P281, P305+351+338
Xn N
R-phrases R22, R36, R51/53, R63
S-phrases S36/37, S46, S61
NFPA 704
Flammability code 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g., canola oil Health code 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g., chloroform Reactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogen Special hazards (white): no codeNFPA 704 four-colored diamond
1
2
0
Flash point > 100 °C (212 °F; 373 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Myclobutanil is a triazole chemical used as a fungicide.[1] It is a steroid demethylation inhibitor, specifically inhibiting ergosterol biosynthesis. Ergosterol is a critical component of fungal cell membranes.

References

  1. ↑ Myclobutanil, PAN Pesticides Database


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