| 词条 | Myclobutanil | ||||
| 释义 |
| Verifiedfields = changed | Watchedfields = changed | ImageFile = Myclobutanil Grundstruktur V1.svg | ImageSize = 150px | ImageFile_Ref = {{chemboximage|correct|??}} | ImageName = Kekulé, skeletal formula of myclobutanil | IUPACName = 2-(4-Chlorophenyl)-2-(1,2,4-triazol-1-ylmethyl)hexanenitrile | OtherNames = |Section1={{Chembox Identifiers | CASNo = 88671-89-0 | CASNo_Ref = {{cascite|correct|CAS}} | PubChem = 6336 | PubChem1 = 11077077 | PubChem1_Comment = (2R) | PubChem2 = 38989055 | PubChem2_Comment = (2S) | ChemSpiderID = 6096 | ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} | ChemSpiderID1 = 9252226 | ChemSpiderID1_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID1_Comment = (2R) | EINECS = 410-400-0 | UNNumber = 3077 | KEGG = C18477 | KEGG_Ref = {{keggcite|correct|kegg}} | ChEBI_Ref = {{ebicite|changed|EBI}} | ChEBI = 75281 | MeSHName = Systhane | RTECS = XZ5257000 | Beilstein = 7138849 | SMILES = CCCCC(Cn1cncn1)(C#N)c1ccc(Cl)cc1 | StdInChI = 1S/C15H17ClN4/c1-2-3-8-15(9-17,10-20-12-18-11-19-20)13-4-6-14(16)7-5-13/h4-7,11-12H,2-3,8,10H2,1H3 | StdInChI_Ref = {{stdinchicite|changed|chemspider}} | StdInChIKey = HZJKXKUJVSEEFU-UHFFFAOYSA-N | StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} }} |Section2={{Chembox Properties | C=15 | H=17 | N=4 | Cl=1 | Appearance = Pale, yellow, translucent crystals | MeltingPtC = 63 to 68 | BoilingPtC = 202 to 208 | BoilingPt_notes = at 130 Pa | Solubility = 142{{nbsp}}mg⋅dm−3 }} |Section3={{Chembox Hazards | GHSPictograms = {{GHS exclamation mark}} {{GHS health hazard}} {{GHS environment}} | GHSSignalWord = Warning | HPhrases = {{H-phrases|302|319|361|411}} | PPhrases = {{P-phrases|273|281|305+351+338}} | NFPA-H = 2 | NFPA-F = 1 | NFPA-R = 0 | FlashPt = > | FlashPtC = 100 }} | verifiedrevid = 462256248 }}Myclobutanil is a triazole chemical used as a fungicide. It is a steroid demethylation inhibitor, specifically inhibiting ergosterol biosynthesis.[1] Ergosterol is a critical component of fungal cell membranes. When heated, myclobutanil decomposes to produce corrosive and/or toxic fumes, including carbon monoxide, carbon dioxide, hydrogen chloride, hydrogen cyanide, and nitrogen oxides.[2][3] Myclobutanil is banned in Canada, Colorado, Washington, and Oregon for the production of medical and recreational marijuana; however, despite the Canadian ban, myclobutanil has been discovered in medical marijuana produced by at least one government licensed grower.[4] In Michigan, the current state action limit for myclobutanil is 200 ppb in cannabis products. [5] Stereoisomerism
References1. ^{{cite web | url = http://www.kingtaichem.com/pro_f_MYCLOBUTANIL.htm | publisher = Kingtai Chemicals Co. | title = Myclobutanil Product Sheet}} 2. ^{{cite web|url=https://cameochemicals.noaa.gov/chemical/30020|title=MYCLOBUTANIL - CAMEO Chemicals - NOAA|first=NOAA Office of Response and Restoration, US|last=GOV|website=cameochemicals.noaa.gov}} 3. ^{{cite web | url = http://www.dow.com/webapps/include/GetDoc.aspx?filepath=productsafety/pdfs/noreg/233-01023.pdf&pdf=true | title = Product Safety Assessment: Myclobutanil}} 4. ^{{cite web|url=https://www.theglobeandmail.com/news/national/canadians-not-told-about-banned-pesticide-found-in-medical-marijuana-supply/article33443887/|title=Canadians not told about banned pesticide found in medical pot supply|publisher=|via=The Globe and Mail}} 5. ^{{cite web|url=https://www.michigan.gov/documents/lara/Department_Banned_Pesticide_Active_Ingredient_List_620039_7.pdf&pdf=true | title = Technical Bulletin}} External links
2 : Fungicides|Triazoles |
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