N,N-ジメチルチオカルバミン酸S-(4-フェノキシブチル)

N,N-ジメチルチオカルバミン酸S-(4-フェノキシブチル) 価格 もっと(4)

メーカー	製品番号	製品説明	CAS番号	包装	価格	更新時間	購入
富士フイルム和光純薬株式会社(wako)	W01W0106-0596	フェノチオカルブ標準品 98.0+% (capillary GC) 98.0+% (qNMR) Fenothiocarb Standard 98.0+% (capillary GC) 98.0+% (qNMR)	62850-32-2	100mg	￥10000	2024-03-01	購入
関東化学株式会社(KANTO)	16204-97	フェノチオカルブ標準品 >98.0%(GC) Fenothiocarb standard >98.0%(GC)	62850-32-2	100mg	￥10000	2024-03-01	購入
Sigma-Aldrich Japan	32475	PESTANAL?, analytical standard Fenothiocarb PESTANAL?, analytical standard	62850-32-2	25mg	￥40700	2021-03-23	購入
林純薬工業株式会社	99052751	フェノチオカルブ Fenothiocarb	62850-32-2	100mg	￥20000	2024-03-01	購入

N,N-ジメチルチオカルバミン酸S-(4-フェノキシブチル) 化学特性,用途語,生産方法

外観

白色, 結晶～結晶性粉末

溶解性

エタノール及びアセトンに溶け、水にほとんど溶けない。

農薬用途

ダニ駆除剤

使用

Fenothiocarb is an acaricide used to control the eggs and young stages of Panonychus citri, Panonychus ulmi and other Panonychus spp.

代謝経路

When the red mite, applied with 14C-fenothiocarb by the contact method, metabolizes fenothiocarb, resulting in several metabolites via the primary oxidation of the N-methyl moiety. The photodegradation of fenothiocarb on silica gel plate exposed to sunlight gives rise to several degradation products. A primary photochemical reaction seems to be the oxidation of the sulfur atom to form its sulfoxide. Under greenhouse conditions, when fenothiocarb is applied to the citrus trees, the major metabolites identified in the leaves, rinds, and edible fruit are 6-O-malonyl-b-D-glucosode of N- hydroxymethyl fenothiocarb, N-formylfenothiocarb, and glucoside conjugate of phenol (not shown in the map), respectively. In soils, fenothiocarb is more rapidly degraded under upland conditions than under flooded conditions. Main degradation pathways include oxidation of the sulfur atom which results in the formation of methyl-4-phenoxybutylsulfoxide, its sulfone, and 4-phenoxybutylsulfonic acid.

Degradation

Fenothiocarb has long residual activity. It is stable to hydrolysis for 5 days (pH 5-9, 40 °C) but it is decomposed slowly by sunlight (PM). [U-¹⁴C-phenyl]Fenothiocarb was applied to the origin of silica gel TLC plates and exposed to sunlight in September or October. The plates were developed, with authentic standard compounds also applied, in two dimensions using different solvent systems. After 72 hours exposure to sunlight, 34% of parent fenothiocarb remained (DT₅₀ 45 hours). Twelve photoproducts were detected. Products that were identified are illustrated in Scheme 1 and were N-formyl-fenothiocarb (2), desmethyl-fenothiocarb (3) the bis(4-phenoxybutyl) thiolsulfinate (4), the bis(4-phenoxybutyl) thiolsulfonate (5), the sulfoxide derivative (6) and 4-phenoxybutanesulfonic acid (7). The latter two compounds were major products. The primary photochemical reaction was oxidation of sulfur to form fenothiocarb sulfoxide (6) followed by cleavage of the ester linkage and the oxidation or dimerisation of the 4-phenoxybutanesulfenic acid intermediate. The second main route of photodegradation was oxidation of the N-methyl moiety of fenothiocarb (Unai and Tomiwaza, 1986b).

N,N-ジメチルチオカルバミン酸S-(4-フェノキシブチル) 上流と下流の製品情報

原材料

準備製品

N,N-ジメチルチオカルバミン酸S-(4-フェノキシブチル) 生産企業

名前	電話番号	電子メール	国籍	製品カタログ	優位度
Hubei Jusheng Technology Co.,Ltd.	18871490254	linda@hubeijusheng.com	CHINA	28180	58
Chongqing Chemdad Co., Ltd	+86-023-61398051 +8613650506873	sales@chemdad.com	China	39916	58
career henan chemical co	+86-0371-86658258 15093356674;	factory@coreychem.com	China	29826	58
Shaanxi Dideu Medichem Co. Ltd	+86-29-87569266 15319487004	1015@dideu.com	China	2263	58
TargetMol Chemicals Inc.	+1-781-999-5354 +1-00000000000	marketing@targetmol.com	United States	19892	58
Hebei Duling International Trade Co. LTD	+8618032673083	sales05@hbduling.cn	China	15745	58
LEAPCHEM CO., LTD.	+86-852-30606658	market18@leapchem.com	China	43348	58
J & K SCIENTIFIC LTD.	010-82848833 400-666-7788	jkinfo@jkchemical.com	China	96815	76
BEST-REAGENT	400-1166-196 18981987031	cdhxsj@163.com	China	11726	57
Hangzhou Sage Chemical Co., Ltd.	+86057186818502 13588463833	info@sagechem.com	China	10269	58

62850-32-2(N,N-ジメチルチオカルバミン酸S-(4-フェノキシブチル))キーワード:

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• 62850-32-2
• bi-5452
• dimethylcarbamothioicacids-(4-phenoxybutyl)ester
• dimethyl-carbamothioicacis-(4-phenoxybutyl)ester
• kco-3001
• phenothiocarb
• FENOTHIOCARB
• PANOCON
• PANOCON(R)
• FENOTHIOCARB STANDARD
• s-4-phenoxybutyldimethylthiocarbamate
• S-（4-phenoxybutyl) dimethylthlocarbamate
• N,N-Dimethylthiocarbamic acid S-(4-phenoxybutyl) ester
• N,N-Dimethylthiocarbamic acid S-4-phenoxybutyl
• Fenothiocard
• CarbaMothioic acid, diMethyl-, S-(4-phenoxybutyl) ester
• N,N-Dimethylcarbamothioic acid S-(4-phenoxybutyl) ester
• S-(4-Phenoxybutyl)-N,N-dimethylthiocarbamate
• Fenothiocarb solution
• FENOTHIOCARB-D6
• Fenothiocarb Solution, 1000ppm
• Fenothiocarb@1000 μg/mL in Acetone
• Fenothiocarb@50 μg/mL in Methanol
• Fenothiocarb@100 μg/mL in Methanol
• Carbamothioic acid, N,N-dimethyl-, S-(4-phenoxybutyl) ester
• Fenothiocarb Solution in Methanol, 100μg/mL
• Avobenzone Impurity 5
• パノコン
• N,N-ジメチルチオカルバミン酸S-4-フェノキシブチル
• N,N-ジメチルチオカルバミン酸S-(4-フェノキシブチル)
• フェノチオカルブ
• Ｓ－４－フェノキシブチルジメチルジチオカルバマート
• フェノチオカルブ標準品
• Ｓ４フェノキシブチルジメチルジチオカルバマト
• N,N-ジメチルチオカルバミン酸S-4-フェノキシブチル　（フェノチオカルブ）
• N,N-ジメチルチオカルバミン酸S-4-フェノキシブチル (別名 フェノチオカルブ)
• N,N-ジメチル[(4-フェノキシブチル)スルファニル]ホルムアミド
• カーバメート系殺虫剤
• 殺ダニ剤
• 農薬類，殺虫剤および除草剤など
• 生活関係標準物質
• 食料品
• 有機標準物質