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氯亚胺硫磷 | 10311-84-9

中文名称
氯亚胺硫磷
中文别名
S-(2-氯-1-酞酰亚胺基乙基)O,O-二乙基二硫代磷酸酯;氯亚磷;酰亚胺;氯甲亚胺硫磷;氯乙亚胺磷
英文名称
dialifos
英文别名
O,O-diethyl S-(2-chloro-1-phthalimidoethyl)phosphorodithioate;Dialifor;2-(2-chloro-1-diethoxyphosphinothioylsulfanylethyl)isoindole-1,3-dione
氯亚胺硫磷化学式
CAS
10311-84-9
化学式
C14H17ClNO4PS2
mdl
MFCD00055503
分子量
393.852
InChiKey
MUMQYXACQUZOFP-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 稳定性/保质期:

    遵照规格使用和储存,则不会分解。

计算性质

  • 辛醇/水分配系数(LogP):
    3.8
  • 重原子数:
    23
  • 可旋转键数:
    8
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.428
  • 拓扑面积:
    113
  • 氢给体数:
    0
  • 氢受体数:
    6

ADMET

代谢
Torak ... 在给奶牛饲料中添加(5 ppm)连续4天之后,几乎完全被代谢。3%的未改变 ... 从粪便中回收。... 尿液中二乙基硫代磷酰氧酯占剂量的33%;仅检测到微量的二乙基磷酸盐。与牛肉肝脏制剂一起孵化 ... 产生二乙基硫代磷酰氧酯 ... .
Torak ... was almost completely metabolized when admin to dairy cow in feed (5 ppm) for 4 days. 3% of unchanged ... recovered from feces. ... urinary diethyl phosphorothionate accounted for 33% of the dose; only traces of diethyl phosphate were detected. Incubation ... with beef-liver prepn ... yielded diethyl phosphorothionate ... .
来源:Hazardous Substances Data Bank (HSDB)
代谢
... /Torak/ 在新鲜瘤胃液存在的情况下8小时后未发生变化 ... .
... /Torak/ was unchanged after 8 hr in presence of fresh rumen fluid ... .
来源:Hazardous Substances Data Bank (HSDB)
代谢
第一步代谢反应是将...氧化成硫代磷酸盐。
First metabolic step is ... oxidation to the thiophosphate.
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 副作用
其他毒物 - 有机磷酸酯
Other Poison - Organophosphate
来源:Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
毒理性
  • 解毒与急救
气道保护。确保呼吸道通畅。必要时对病人进行气管插管,并使用大口径吸痰设备吸出分泌物。如果呼吸抑制,通过机械辅助肺通气给予氧气。在给予阿托品之前尽可能提高组织氧合,以最小化心室颤动的风险。在严重中毒的情况下,可能需要机械支持肺通气数天。/有机磷农药/
Airway protection. Insure that a clear airway exists. Intubate the patients and aspirate the secretions with a large-bore suction device if necessary. Administer oxygen by mechanically assisted pulmonary ventilation if respiration is depressed. Improve tissue oxygenation as much as possible before administering atropine, so as to minimize the risk of ventricular fibrillation. In severe poisonings, it may be necessary to support pulmonary ventilation mechanically for several days. /Organophosphate pesticides/
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 解毒与急救
硫酸阿托品。如果不能静脉注射,可以通过静脉或肌肉注射硫酸阿托品。请记住,如果初次静脉通路难以获得,阿托品可以通过气管内导管给药。... 阿托品不能重新激活胆碱酯酶酶或加速有机磷的消除。如果有机磷的组织浓度在阿托品效果消失时仍然很高,可能会再次出现中毒症状。阿托品对毒蕈碱样症状有效,但对烟碱样作用无效,特别是肌肉无力和抽搐以及呼吸抑制。尽管有这些局限性,阿托品在有机磷中毒中常常是救命药物。... 据报道,雾化阿托品的辅助使用可以改善呼吸窘迫,减少支气管分泌物,并增加氧合。/有机磷农药/
Atropine sulfate. Administer atropine sulfate intravenously, or intramuscularly if intravenous injection is not possible. Remember that atropine can be administered through an endotracheal tube if initial IV access if difficult to obtain. ... Atropine does not reactivate the cholinesterase enzyme or accelerate disposition of organophosphate. Recrudescence of poisoning may occur if tissue concentrations of organophosphate remain high when the effect of atropine wears off. Atropine is effective against muscarinic manifestations, but it is ineffective against nicotinic actions, specifically muscle weakness and twitching, and respiratory depression. Despite the limitations, atropine is often a life-saving agent in organophosphate poisonings. ... The adjunctive use of nebulized atropine has been reported to improve respiratory distress, decrease bronchial secretions, and increase oxygenation. /Organophosphate pesticides/
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 解毒与急救
格隆吡咯酸被研究作为阿托品的替代品,并发现使用持续输注时具有相似的结果。将格隆吡咯酸的安瓿加入生理盐水中,并根据干燥的粘膜和每分钟心率超过60次的效果来调整输注量。在此研究中,当心率低于60次/分钟时,使用阿托品作为一次性注射。这种方案另一个明显的优势是减少了呼吸系统感染的数量。/有机磷农药/
Glycopyrolate has been studied as an alternative to atropine and found to have similar outcomes using continuous infusion. Ampules of ... glycopyrolate were added to ... saline and this infusion was titrated to the desired effects of dry mucous membranes and heart rate above 60 beats/min. During this study, atropine was used as a bolus for a heart rate less than 60 beats/min. The other apparent advantage to this regimen was a decreased number of respiratory infections. ... /Organophosphate pesticides/
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 解毒与急救
普瑞洛辛。在给予普瑞洛辛之前,抽取一个血液样本(用肝素化)进行胆碱酯酶分析(因为普瑞洛辛倾向于逆转胆碱酯酶的抑制)。在严重有机磷农药中毒的情况下,如果出现呼吸抑制、肌肉无力 和/或 抽搐严重,给予普瑞洛辛(普罗帕姆,2-PAM),这是一种胆碱酯酶复活剂。如果早期给药(通常在中毒后48小时内),普瑞洛辛可以缓解中毒的尼古丁和毒蕈碱效应。普瑞洛辛通过重新激活胆碱酯酶,并且通过减慢磷酸化胆碱酯酶到不可复活形式的“老化”过程来起作用。... 普瑞洛辛的剂量可能在1-2小时后重复给药,然后在需要时每10-12小时给药一次。在非常严重的中毒情况下,剂量可能加倍。通常需要重复给予普瑞洛辛。在涉及继续吸收有机磷(如摄入大量后)或高度亲脂性有机磷从脂肪转移到血液的情况下,可能需要在通常认为其有效性的限制,即暴露后48小时的时间之外,继续给予普瑞洛辛几天。... 在给药期间应监测血压,因为偶尔会发生高血压危机。如果血压升至危险水平,应减慢或停止给药。如果普瑞洛辛给药期间或给药后出现呼吸抑制,应准备机械辅助呼吸。如果静脉注射不可能,普瑞洛辛可以通过深层肌肉注射给药。/有机磷农药/
Pralidoxime. Before administration of pralidoxime, draw a blood sample (heparinized) for cholinesterase analysis (since pralidoxime tends to reverse the cholinesterase depression). Administer pralidoxime (Protopam, 2-PAM), a cholinesterase reactivator, in cases of severe poisoning by organophosphate pesticides in which respiratory depression, muscle weakness, and/or twitching are severe. When administered early (usually less than 48 hours after poisoning) pralidoxime relieves the nicotinic as well as the muscarinic effects of poisoning. Pralidoxime works by reactivating the cholinesterase and also by slowing the "aging" process of phosphorylated cholinesterase to a non-reactivatable form. ... Dosage of pralidoxime may be repeated in 1-2 hours, then at 10-12 hour intervals if needed. In very severe poisonings, dosage rates may be doubled. Repeated doses of pralidoxime are usually required. In cases that involve continuing absorption of organophosphate (as after ingestion of large amounts), or continuing transfer of highly lipophilic organophosphate from fat into blood, it may be necessary to continue administration of pralidoxime for several days beyond the 48 hour post-exposure interval usually cited as the limit of its effectiveness. ... Blood pressure should be monitored during administration because of the occasional occurrence of hypertensive crisis. Administration should be slowed or stopped if blood pressure rises to hazardous levels. Be prepared to assist pulmonary ventilation mechanically if respiration is depressed during or after pralidoxime administration. If intravenous injection is not possible, pralidoxime may be given by deep intramuscular injection. /Organophosphate pesticides/
来源:Hazardous Substances Data Bank (HSDB)
吸收、分配和排泄
Torak ... 在给奶牛饲料中添加(5 ppm)连续4天之后,几乎完全被代谢。3%的未改变的/Torak/从粪便中回收,但在尿液或牛奶中没有发现。/Torak/
Torak ... was almost completely metabolized when admin to dairy cow in feed (5 ppm) for 4 days. 3% of unchanged /Torak/ recovered from feces, but none was found in urine or milk. /Torak/
来源:Hazardous Substances Data Bank (HSDB)
吸收、分配和排泄
在哺乳动物中,口服给药后,敌百虫会迅速被消除,主要是以邻苯二甲酸盐的形式通过尿液排出。
In mammals, following oral administration, dialifos is rapidly eliminated, principally in the urine, as the o-phthalic acid salt.
来源:Hazardous Substances Data Bank (HSDB)

安全信息

  • 储存条件:
    密封于阴凉干燥处。

制备方法与用途

制备方法

用于苹果、柑橘、葡萄和蔬菜上的螨类害虫防治。

用途简介

暂无详细信息。

用途

适用于苹果、柑橘、葡萄和蔬菜上防治螨类害虫。

文献信息

  • [EN] MICROBIOCIDAL OXADIAZOLE DERIVATIVES<br/>[FR] DÉRIVÉS D'OXADIAZOLE MICROBIOCIDES
    申请人:SYNGENTA PARTICIPATIONS AG
    公开号:WO2017157962A1
    公开(公告)日:2017-09-21
    Compounds of the formula (I) wherein the substituents are as defined in claim 1, useful as a pesticides, especially fungicides.
    式(I)的化合物,其中取代基如权利要求1所定义,作为杀虫剂特别是杀菌剂有用。
  • Thieno-pyrimidine compounds having fungicidal activity
    申请人:Brewster Kirkland William
    公开号:US20070093498A1
    公开(公告)日:2007-04-26
    The present invention relates to thieno[2,3-d]-pyrimidine compounds having fungicidal activity.
    本发明涉及具有杀真菌活性的噻吩[2,3-d]-嘧啶化合物。
  • [EN] INSECTICIDAL TRIAZINONE DERIVATIVES<br/>[FR] DÉRIVÉS DE TRIAZINONE INSECTICIDES
    申请人:SYNGENTA PARTICIPATIONS AG
    公开号:WO2013079350A1
    公开(公告)日:2013-06-06
    Compounds of the formula (I) or (I'), wherein the substituents are as defined in claim 1, are useful as pesticides.
    式(I)或(I')的化合物,其中取代基如权利要求1所定义的那样,可用作杀虫剂。
  • THIENYLPYRIDYLCARBOXAMIDES
    申请人:Dunkel Ralf
    公开号:US20110105564A1
    公开(公告)日:2011-05-05
    Novel thienylpyridylcarboxamides of the formula (I) The present application is also directed to a plurality of processes for preparing these compounds and their use for controlling unwanted microorganisms, and also novel intermediates and their preparation.
    新型噻吩基吡啶基羧酰胺的化学式(I) 本申请还涉及多种制备这些化合物的方法,以及它们用于控制不受欢迎的微生物的用途,还有新颖的中间体及其制备。
  • [EN] ISOXAZOLINE DERIVATIVES AS INSECTICIDES<br/>[FR] DÉRIVÉS D'ISOXAZOLINE EN TANT QU'INSECTICIDES
    申请人:SYNGENTA PARTICIPATIONS AG
    公开号:WO2011101402A1
    公开(公告)日:2011-08-25
    The present invention relates to compounds formula (I), wherein P is P1, P2, heterocyclyl or heterocyclyl substituted by one to five Z; and wherein A1, A2, A3, A4, G1, R1, R2, R3, R4, R5, R6, R17, R18, R19 and R20 are as defined in claim 1; or a salt or N-oxide thereof. Furthermore, the present invention relates to processes and intermediates for preparing compounds of formula (I), to insecticidal, acaricidal, nematicidal and molluscicidal compositions comprising the compounds of formula (I) and to methods of using the compounds of formula (I) to control insect, acarine, nematode and mollusc pests.
    本发明涉及化合物式(I),其中P为P1、P2、杂环烷基或被一到五个Z取代的杂环烷基;以及其中A1、A2、A3、A4、G1、R1、R2、R3、R4、R5、R6、R17、R18、R19和R20如权利要求1中所定义;或其盐或N-氧化物。此外,本发明涉及制备化合物式(I)的过程和中间体,包括化合物式(I)的杀虫剂、杀螨剂、杀线虫剂和杀软体动物剂组合物,以及使用化合物式(I)控制昆虫、螨虫、线虫和软体动物害虫的方法。
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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mass
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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