摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

butocarboxime | 34681-10-2

中文名称
——
中文别名
——
英文名称
butocarboxime
英文别名
3-(methylthio)butanone O-methylcarbamoyloxime;butocarboxim;3-(Methylthio)-2-butanone O-(methylcarbamoyl)oxime;[(E)-3-methylsulfanylbutan-2-ylideneamino] N-methylcarbamate
butocarboxime化学式
CAS
34681-10-2
化学式
C7H14N2O2S
mdl
——
分子量
190.266
InChiKey
SFNPDDSJBGRXLW-WEVVVXLNSA-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

  • 熔点:
    25 °C
  • 密度:
    1.2118 (rough estimate)
  • 颜色/状态:
    Pale brown, viscous liquid (tech.). Crystalline at lower temperatures. /Technical butocarboxim/
  • 溶解度:
    In water, 35 g/l @ 20 °C
  • 蒸汽压力:
    7.95X10-5 mm Hg @ 20 °C
  • 稳定性/保质期:

    Stable at pH 5-7 (up to 50 °C), but hydrolysed by strong acids and alkalis. Stable to sunlight and oxygen. Thermally stable up to 100 °C.

  • 分解:
    When heated to decomposition it emits toxic fumes of /nitrogen and sulfur oxides/.

计算性质

  • 辛醇/水分配系数(LogP):
    1.2
  • 重原子数:
    12
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    76
  • 氢给体数:
    1
  • 氢受体数:
    4

ADMET

代谢
在哺乳动物中,口服给药后,代谢为丁氧羧基咪唑,并以丁氧羧基咪唑及其...产物形式通过尿液排出。
In mammals, following oral administration, metabolised to butoxycarboxim, and excreted in the urine as butoxycarboxim and its...products.
来源:Hazardous Substances Data Bank (HSDB)
代谢
碳酰胺的代谢第一步是解成碳酸酰胺酸,该酸会分解成二氧化碳CO2)和相应的胺。N-甲基和N, N-二甲基衍生物解机制不同。N-甲基碳酰胺会通过异氰酸中间体,而在N, N-二甲基碳酰胺的解中,会形成与羟基离子加成的产物,产生醇和N-二甲基取代酸。酯酶催化的解速率在哺乳动物中比植物和昆虫快。除了解,还会发生氧化,包括:芳香环的羟基化,O-脱烷基化,N-甲基羟基化,N-脱烷基化,脂肪族侧链的氧化,以及磺化成相应的磺酮。氧化与混合功能氧化酶(MFO)酶相关。共轭作用在哺乳动物中导致O-和N-葡萄糖苷酸、硫酸盐和巯基尿酸生物的形成。糖苷和磷酸盐是植物中更常见的共轭产物。/碳酰胺杀虫剂/
The first step in the metabolism of carbamates is hydrolysis to carbamic acid, which decomposes to carbon dioxide (CO2) and the corresponding amine. The mechanism of hydrolysis is different for N -methyl and N -dimethyl derivatives. The N -methyl carbamates pass through an isocyanate intermediate, whereas in the hydrolysis of N - dimethylcarbamates, an addition product with a hydroxyl ion is formed yielding the alcohol and N -dimethyl substituted acid. The rate of hydrolysis by esterases is faster in mammals than in plants and insects. Apart from hydrolysis, oxidation also takes place including: hydroxylation of the aromatic ring, O -dealkylation, N -methyl hydroxylation, N -dealkylation, oxidation of aliphatic side chains, and sulfoxidation to the corresponding sulfone. Oxidation is associated with the mixed-function oxidase (MFO) enzymes. Conjugation leads to the formation of O - and N -glucuronides, sulfates, and mercapturic acid derivatives in mammals. Glycosides and phosphates are conjugation products more common in plants. /Carbamate Pesticides/
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 副作用
其他毒药 - 氨基甲酸
Other Poison - Carbamate
来源:Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
毒理性
  • 毒性数据
LC50 (大鼠) = 1000毫克/立方米/4小时
LC50 (rat) = 1,000 mg/m3/4h
来源:Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
毒理性
  • 解毒与急救
基本治疗:建立专利气道。如有必要,进行吸痰。可能需要积极控制气道。观察呼吸不足的迹象,如有必要,协助通气。通过非循环呼吸面罩以10至15升/分钟的速度给予氧气。监测肺肿,并在必要时进行治疗……。监测休克并在必要时治疗……。预期癫痫发作并在必要时治疗……。对于眼睛污染,立即用冲洗眼睛。在转运过程中,用生理盐连续冲洗每只眼睛……。不要使用催吐剂。对于误食,如果患者能吞咽、有强烈的干呕反射且不流口,则用冲洗口腔,并给予5毫升/千克,最多200毫升的进行稀释。给予活性炭……。/氨基甲酸酯和相关化合物/
Basic treatment: Establish a patent airway. Suction if necessary. Aggressive airway control may be needed. Watch for signs of respiratory insufficiency and assist ventilations if necessary. Administer oxygen by nonrebreather mask at 10 to 15 L/min. Monitor for pulmonary edema and treat if necessary ... . Monitor for shock and treat if necessary ... . Anticipate seizures and treat if necessary ... . For eye contamination, flush eyes immediately with water. Irrigate each eye continuously with normal saline during transport ... . Do not use emetics. For ingestion, rinse mouth and administer 5 ml/kg up to 200 ml of water for dilution if the patient can swallow, has a strong gag reflex, and does not drool. Administer activated charcoal ... . /Carbamates and related compounds/
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 解毒与急救
高级治疗:对于无意识的病人,考虑进行口咽或鼻咽气管插管以控制气道。使用气囊面罩装置的正压通气技术可能有益。监测心率和必要时治疗心律失常。开始静脉输液,使用5%葡萄糖/生理盐维持通道,最小流量。如果出现低血容量的迹象,使用乳酸钠林格氏液。对于低血压,如果出现低血容量的迹象,谨慎给予液体。注意肺肿的迹象。给予阿托品。在给药前纠正低氧血症。在严重中毒的患者中,给予定(2 PAM)。仅限医生直接指令。用足够的阿托品化和纠正低氧血症来治疗癫痫。很少需要使用地西泮。使用丙美卡因化物协助眼睛冲洗。/氨基甲酸酯和相关化合物/
Advanced treatment: Consider orotracheal or nasotracheal intubation for airway control in the patient who is unconscious. Positive pressure ventilation techniques with a bag valve mask device may be beneficial. Monitor cardiac rhythm and treat arrhythmias if necessary ... . Start an IV with D5W /SRP: "To keep open", minimal flow rate/. Use lactated Ringer's if signs of hypovolemia are present. For hypotension if signs of hypovolemia are present, administer fluid cautiously. Watch for signs of pulmonary edema ... . Administer atropine. Correct hypoxia before administration ... . In severely poisoned patients, administer pralidoxime chloride (2 PAM). DIRECT PHYSICIAN ORDERS ONLY ... . Treat seizures with adequate atropinization and correction of hypoxia. Rarely is diazepam necessary ... . Use proparacaine hydrochloride to assist eye irrigation ... . /Carbamates and related compounds/
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 解毒与急救
人工呼吸(通过气管插管)应在呼吸衰竭的第一个迹象出现时开始,并持续尽可能长的时间。建议谨慎给予液体,以及一般的支持性和对症药物治疗,并绝对休息。/氨基甲酸酯类杀虫剂/
Artificial respiration (via a tracheal tube) should be started at the first sign of respiratory failure and maintained for as long as necessary. Cautious administration of fluids is advised as well as general supportive and symptomatic pharmacological treatment and absolute rest. /Carbamate pesticides/
来源:Hazardous Substances Data Bank (HSDB)
吸收、分配和排泄
目前关于哺乳动物通过吸入或口服途径接触后,氨基甲酸盐在各器官和组织的分布情况的信息很少。报告有残留物的器官包括肝脏、肾脏、大脑、脂肪和肌肉。在大鼠体内的半衰期约为3-8小时。看来人类通过尿液排出氨基甲酸盐的速度也很快,而且人类的代谢途径与大鼠相同。/氨基甲酸酯类杀虫剂/
Little information is available on the distribution of carbamates in the various organs and tissues in mammals following exposure by inhalation or the oral route. The organs in which residues have been reported are the liver, kidneys, brain, fat, and muscle. The half-life in the rat is of the order of 3-8 hr. ...It seems that the excretion of carbamates via urine is also rapid in man, and that the metabolic pathways in man are the same as those in the rat. /Carbamate Pesticides/
来源:Hazardous Substances Data Bank (HSDB)

安全信息

  • 危险等级:
    6.1(b)
  • 危险品标志:
    N,T
  • 安全说明:
    S36/37,S45,S60,S61
  • 危险类别码:
    R10,R36,R50/53,R23/24/25
  • WGK Germany:
    3
  • 危险品运输编号:
    2757
  • RTECS号:
    EL9215000
  • 海关编码:
    2930909051
  • 包装等级:
    III
  • 危险类别:
    6.1(b)

制备方法与用途

理化性质

淡棕色黏稠性液体,在低温下结晶。(E)-异构体熔点为37℃,(Z)-异构体在室温下呈油状。异构体混合物的蒸汽压为10.6mPa(20℃),相对密度为1.12(20℃)。Kow lgP值为1.1。亨利常数为5.76×10^(-4) Pa·m³/mol。在中溶解度为35g/L(20℃)。其他溶剂中的溶解度较低,脂肪族化合物中溶解度约为11g/L,可与芳烃酯类酮类混合。该物质在日光下于pH 5~7的环境下直到50℃时稳定,在强酸碱性条件下易解,在光照和氧气存在下稳定,并且在100℃以下对热稳定。

应用 适用作物

丁酮威适用于果树、蔬菜、谷物、棉花、烟草及观赏植物等作物的防治。

防治对象

主要防治蚜虫、牧草虫、粉虱、蚧壳虫以及一些吸吮昆虫等害虫。

推荐使用情况
  • 在我国,以125kg/hm²剂量用于防治棉花上的棉粉虱效果优良。
  • 对于果树、观赏植物和蔬菜上的蚜虫,推荐用量为50~75g/L,具有良好的活性。对螨类的活性则中等。
毒性 急性毒性
  • 大鼠经口LD₅₀值为153~215mg/kg。
  • 兔子经皮LD₅₀值为360mg/kg,对眼睛有刺激作用。
  • 大鼠吸入LC₅₀(4h)为1mg/L空气。
慢性毒性
  • 在大鼠和狗的90天喂养试验中,无作用剂量均为饲喂100mg/kg饲料。
  • 高剂量(300mg/kg饲料)在2年的饲喂实验中未表现出致癌作用,并对生育力、生长速度或死亡率无任何影响。
ADI值
  • 按BfR规定,ADI为0.02mg/kg[1990]。
  • Ames试验结果表明该物质无诱变性。
环境代谢 动物代谢

动物经口摄入后会代谢成丁酮飙威,通过尿液排出体外。其降解产物同样随着尿液排出。

植物与土壤中的降解情况

植物和土壤中的降解过程相同。

土壤中降解时间

在土壤中,DT₅₀(半衰期)为1~8天。代谢物的DT₅₀约为16~44天。在土壤中甲基部分断裂开,原子被氧化成亚磺酸磺酸根。

通过上述分解过程,该化合物可以在环境中较快地降解,减少对环境的影响。

文献信息

  • [EN] BICYCLYL-SUBSTITUTED ISOTHIAZOLINE COMPOUNDS<br/>[FR] COMPOSÉS ISOTHIAZOLINE SUBSTITUÉS PAR UN BICYCLYLE
    申请人:BASF SE
    公开号:WO2014206910A1
    公开(公告)日:2014-12-31
    The present invention relates to bicyclyl-substituted isothiazoline compounds of formula (I) wherein the variables are as defined in the claims and description. The compounds are useful for combating or controlling invertebrate pests, in particular arthropod pests and nematodes. The invention also relates to a method for controlling invertebrate pests by using these compounds and to plant propagation material and to an agricultural and a veterinary composition comprising said compounds.
    本发明涉及公式(I)中变量如索权和说明中所定义的自行车基取代异噻唑啉化合物。这些化合物对抗或控制无脊椎动物害虫,特别是节肢动物害虫和线虫方面具有用途。该发明还涉及一种通过使用这些化合物来控制无脊椎动物害虫的方法,以及包含所述化合物的植物繁殖材料、农业和兽医组合物。
  • [EN] AZOLINE COMPOUNDS<br/>[FR] COMPOSÉS AZOLINE
    申请人:BASF SE
    公开号:WO2015128358A1
    公开(公告)日:2015-09-03
    The present invention relates to azoline compounds of formula (I) wherein A, B1, B2, B3, G1, G2, X1, R1, R3a, R3b, Rg1 and Rg2 are as defined in the claims and the description. The compounds are useful for combating or controlling invertebrate pests, in particular arthropod pests and nematodes. The invention also relates to a method for controlling invertebrate pests by using these compounds and to plant propagation material and to an agricultural and a veterinary composition comprising said compounds.
    本发明涉及式(I)的噁唑啉化合物,其中A、B1、B2、B3、G1、G2、X1、R1、R3a、R3b、Rg1和Rg2如权利要求和描述中所定义。这些化合物对抗或控制无脊椎动物害虫,特别是节肢动物害虫和线虫方面具有用途。该发明还涉及一种利用这些化合物控制无脊椎动物害虫的方法,以及包括所述化合物的植物繁殖材料、农业和兽医组合物。
  • [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
查看更多