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氯菊酯

氯菊酯用途

【用途一】
为高效、低毒杀虫剂,用于防治棉花、水稻、蔬菜、果树、茶树等多种作物害虫,也能防治卫生及牲畜害虫
【用途二】
有较强的触杀和胃毒作用,具有击倒力强、杀虫速度快的特点。对光较稳定,在同等使用条件下,对害虫抗性发展也较缓慢,对鳞翅目幼虫高效。可用于蔬菜、茶叶、果树、棉花等作物防治菜青虫、蚜虫、棉铃虫、棉红铃虫、棉蚜、绿盲蝽、黄条跳甲、桃小食心虫、柑橘潜叶蛾、二十八星瓢虫、茶尺蠖、茶毛虫、茶细蛾等多种害虫,对蚊、蝇、跳蚤、蟑螂、虱子等卫生害虫也有良好的效果。如防治棉铃虫、棉红铃虫,在卵孵盛期,用10%乳油1000~1250倍液喷雾,兼治造桥虫、卷叶虫。防治棉蚜于成虫、若虫盛发期,用10%乳油2000~3000倍液喷雾,对抗性棉蚜和棉铃虫效果较差。防治果树害虫,用10%乳油3.75mL/100m2,对水5.52kg喷雾。防治卫生害虫,用10%乳油800~1000倍液喷雾。防治菜青虫、桃蚜、小菜蛾、斜纹夜蛾等用10%乳油1000~2000倍液喷雾。
【用途三】
该品为高效低毒杀虫剂,用于防治棉花、水稻、蔬菜、果树茶树等多种作物害虫,也用于防治卫生害虫及牲畜害虫。杀虫作用强烈,很低的浓度即可使害虫中毒死亡,农业上治虫有效的浓度大多数都在100ppm以下,一般为20-50ppm,每亩有效成份的用量一般只有5-10ml。
【用途四】
该品味高效低毒杀虫剂,用于防治棉花,水稻,蔬菜果树茶树等多种作物害虫,也用于防治卫生害虫及牲畜害虫。杀虫作用强烈,很低的浓度即可使害虫及中间体较易得到,农业上治虫有效的浓度大多数都在100ppm以下,一般为20-50ppm,每亩有效成分的用量一般在5-10ml。
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氯菊酯名称

[ CAS 号 ]:
52645-53-1

[ 中文名 ]:
氯菊酯

[ 英文名 ]:
Permethrin

[中文别名 ]:

[英文别名 ]:

氯菊酯生物活性

氯菊酯物理化学性质

[ 密度 ]:
1.3±0.1 g/cm3

[ 沸点 ]:
465.9±45.0 °C at 760 mmHg

[ 熔点 ]:
34-35°C

[ 分子式 ]:
C21H20Cl2O3

[ 分子量 ]:
391.288

[ 闪点 ]:
159.4±27.7 °C

[ 精确质量 ]:
390.078949

[ PSA ]:
35.53000

[ LogP ]:
7.15

[ 外观性状 ]:
无色晶体(但技术产品通常作为一种淡棕色液体供应)

[ 蒸汽压 ]:
0.0±1.2 mmHg at 25°C

[ 折射率 ]:
1.616

[ 储存条件 ]:
库房通风低温干燥,与氧化剂分开储运

[ 稳定性 ]:
Stable. Incompatible with strong oxidising agents.

[ 水溶解性 ]:
insoluble

氯菊酯MSDS

氯菊酯毒性和生态

CHEMICAL IDENTIFICATION

RTECS NUMBER :
GZ1255000
CHEMICAL NAME :
Cyclopropanecarboxylic acid, 3-(2,2-dichlorovinyl)-2,2-dimethyl-, 3-phenoxybenzyl ester, (+-)-, (cis,trans)-
CAS REGISTRY NUMBER :
52645-53-1
LAST UPDATED :
199710
DATA ITEMS CITED :
44
MOLECULAR FORMULA :
C21-H20-Cl2-O3
MOLECULAR WEIGHT :
391.31
WISWESSER LINE NOTATION :
L3TJ A1 A1 B1UYGG CVO1R COR

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
Standard Draize test
ROUTE OF EXPOSURE :
Administration onto the skin
SPECIES OBSERVED :
Rodent - rabbit
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Unreported
SPECIES OBSERVED :
Human - man
DOSE/DURATION :
>4 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
383 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LC50 - Lethal concentration, 50 percent kill
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
485 mg/m3
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Administration onto the skin
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
1750 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
6600 mg/kg
TOXIC EFFECTS :
Behavioral - tremor Behavioral - ataxia
TYPE OF TEST :
LD - Lethal dose
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
>270 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Unreported
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
537 mg/kg
TOXIC EFFECTS :
Behavioral - convulsions or effect on seizure threshold Behavioral - ataxia Behavioral - coma
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
424 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LC50 - Lethal concentration, 50 percent kill
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
685 mg/m3
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Administration onto the skin
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
>10 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
429 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
10 gm/kg
TOXIC EFFECTS :
Behavioral - tremor Behavioral - ataxia
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
31 mg/kg
TOXIC EFFECTS :
Biochemical - Enzyme inhibition, induction, or change in blood or tissue levels - other Enzymes
TYPE OF TEST :
LDLo - Lowest published lethal dose
ROUTE OF EXPOSURE :
Intracerebral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
600 ug/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Unreported
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
680 mg/kg
TOXIC EFFECTS :
Behavioral - convulsions or effect on seizure threshold Behavioral - ataxia Behavioral - coma
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rabbit
DOSE/DURATION :
4 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Administration onto the skin
SPECIES OBSERVED :
Rodent - rabbit
DOSE/DURATION :
>2 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - guinea pig
DOSE/DURATION :
4 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Bird - chicken
DOSE/DURATION :
7 gm/kg
TOXIC EFFECTS :
Behavioral - tremor Behavioral - irritability Gastrointestinal - changes in structure or function of salivary glands
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Bird - quail
DOSE/DURATION :
13500 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Bird - duck
DOSE/DURATION :
11300 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Bird - domestic
DOSE/DURATION :
32 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
33855 mg/kg/26W-C
TOXIC EFFECTS :
Liver - changes in liver weight
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
72 gm/kg/2Y-C
TOXIC EFFECTS :
Liver - other changes Liver - changes in liver weight Biochemical - Enzyme inhibition, induction, or change in blood or tissue levels - other Enzymes
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
2800 mg/kg/7D-I
TOXIC EFFECTS :
Peripheral Nerve and Sensation - recording from peripheral motor nerve Behavioral - muscle weakness Biochemical - Enzyme inhibition, induction, or change in blood or tissue levels - other Enzymes
TYPE OF TEST :
TCLo - Lowest published toxic concentration
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
1500 ug/m3/24H/13W-C
TOXIC EFFECTS :
Brain and Coverings - recordings from specific areas of CNS Blood - changes in leukocyte (WBC) count Biochemical - Enzyme inhibition, induction, or change in blood or tissue levels - phosphatases
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
4 mg/kg/10D-I
TOXIC EFFECTS :
Immunological Including Allergic - decrease in cellular immune response
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Bird - quail
DOSE/DURATION :
1098 mg/kg/7D-C
TOXIC EFFECTS :
Liver - changes in liver weight Nutritional and Gross Metabolic - weight loss or decreased weight gain Biochemical - Enzyme inhibition, induction, or change in blood or tissue levels - hepatic microsomal mixed oxidase (dealkylation, hydroxylation, etc.)
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
DOSE :
250 mg/kg
SEX/DURATION :
female 6-15 day(s) after conception
TOXIC EFFECTS :
Reproductive - Fertility - post-implantation mortality (e.g. dead and/or resorbed implants per total number of implants)
TYPE OF TEST :
Specific locus test
TYPE OF TEST :
Micronucleus test

MUTATION DATA

TEST SYSTEM :
Rodent - mouse
DOSE/DURATION :
150 mg/kg
REFERENCE :
PHABDI Proceedings of the Hungarian Annual Meeting for Biochemistry. (Magyar Kemikusok Egyesulete, Anker Koz 1, 1061 Budapest, Hungary) V.1- 1961- Volume(issue)/page/year: 21,227,1981 *** REVIEWS *** IARC Cancer Review:Animal Inadequate Evidence IMEMDT IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man. (WHO Publications Centre USA, 49 Sheridan Ave., Albany, NY 12210) V.1- 1972- Volume(issue)/page/year: 53,329,1991 IARC Cancer Review:Human No Available Data IMEMDT IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man. (WHO Publications Centre USA, 49 Sheridan Ave., Albany, NY 12210) V.1- 1972- Volume(issue)/page/year: 53,329,1991 IARC Cancer Review:Group 3 IMEMDT IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man. (WHO Publications Centre USA, 49 Sheridan Ave., Albany, NY 12210) V.1- 1972- Volume(issue)/page/year: 53,329,1991 *** U.S. STANDARDS AND REGULATIONS *** EPA FIFRA 1988 PESTICIDE SUBJECT TO REGISTRATION OR RE-REGISTRATION FEREAC Federal Register. (U.S. Government Printing Office, Supt. of Documents, Washington, DC 20402) V.1- 1936- Volume(issue)/page/year: 54,7740,1989
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氯菊酯安全信息

[ 符号 ]:

GHS02, GHS07, GHS09

[ 信号词 ]:
Danger

[ 危害声明 ]:
H225-H302-H312-H319-H332-H411

[ 警示性声明 ]:
P210-P273-P280-P305 + P351 + P338

[ 个人防护装备 ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ 危害码 (欧洲) ]:
Xn: Harmful;N: Dangerous for the environment;T: Toxic;F: Flammable;

[ 风险声明 (欧洲) ]:
R20/22

[ 安全声明 (欧洲) ]:
S13-S24-S36/37/39-S60-S61-S45-S36/37-S16-S7-S26

[ 危险品运输编码 ]:
UN1230 3/PG 2

[ RTECS号 ]:
GZ1255000

[ 海关编码 ]:
2916209022

氯菊酯合成路线

氯菊酯上下游产品

氯菊酯制备

【方法一】
三氯乙醛与异丁烯作用得(I)(II)两个三氯烯醇同分异构体。反应以三氯化铝为催化剂,在低温下进行。在氯化氢存在下,乙腈与无水乙醇作用生成亚氨基乙醚盐酸盐,进一步与无水乙醇反应生成原乙酸三乙酯(III)。在催化剂对甲苯磺酸存在下,加热至114~118℃,反应3h,使(I)转化为(II)。将转位产物与原乙酸三乙酯作用,催化剂为异丁酸,反应温度从110℃上升至150℃,大约12h,在150~155℃反应7~8h,于0.08MPa压力下蒸出前馏分,得3,3-二甲基-4,6,6-三氯己烯-[5]-酸乙酯(V),并伴随(VI)。将(VI)在氯化氢-乙醇溶液中进行开环反应又得(V)。(V)在乙醇钠存在下,于40~45℃反应5h,环合生成2,2-二甲基-3-(2,2-二氯乙烯基)-环丙烷羧酸乙酯(VII),经精馏得纯度较高的二氯菊酸乙酯。在碱液存在下,将(VII)回流反应3h,皂化得相应钠盐(VIII)。(VIII)与氯化间苯氧基苄基三乙胺反应,制得氯菊酯(IX)。反应过程如下:



二氯菊酸的合成可参阅文献[5]。
【方法二】
以三氯乙醛与异丁烯合成1,1,1-三氯-4-甲基-4-戊烯-2-醇,经转位后即得1,1,1-三氯-4-甲基-3-戊烯-2-醇,再与原乙酸三乙酯缩合重排而得3,3-二甲基-4,6,6-三氯-5-已烯酸乙酯,进一步在乙醇钠作用下环合为2,2-二甲基-3-(2,2-二氯乙烯基)环丙烷羧酯乙酯,经皂化成钠盐,再与氯化-3-苯氧基苄基三乙胺反应而制得二氯苯醚菊酯。该法原料及中间体较易得到,工艺过程中操作条件要求较严,产品含量一般在60-80%,加工成3.2%或10%乳油、0.25%粉剂使用。
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氯菊酯海关

[ 海关编码 ]: 2916209022

氯菊酯文献

Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species.

Chem. Res. Toxicol. 23 , 171-83, (2010)

Drug-induced liver injury is one of the main causes of drug attrition. The ability to predict the liver effects of drug candidates from their chemical structures is critical to help guide experimental...

Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).

J. Sci. Ind. Res. 65(10) , 808, (2006)

Drug-induced liver injury (DILI) is a significant concern in drug development due to the poor concordance between preclinical and clinical findings of liver toxicity. We hypothesized that the DILI typ...

Developing structure-activity relationships for the prediction of hepatotoxicity.

Chem. Res. Toxicol. 23 , 1215-22, (2010)

Drug-induced liver injury is a major issue of concern and has led to the withdrawal of a significant number of marketed drugs. An understanding of structure-activity relationships (SARs) of chemicals ...


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公司名:上海吉至生化科技有限公司

区域:上海市奉贤区

价格:
¥428.0/500g ¥128.0/100g

联系人:刘佳

产品详情:氯菊酯(顺反异构体混合物)


公司名:上海源溪生物科技有限公司

区域:上海市浦东新区

价格:
¥需询单/1g

联系人:赖经理

产品详情:Permethrin


公司名:上海脉铂医药科技有限公司

区域:上海市嘉定区

价格:
¥475.0/100mg ¥需询单/1g ¥需询单/1g ¥需询单/1g

联系人:李先生

产品详情:Permethrin


公司名:上海阿拉丁生化科技股份有限公司

区域:上海市浦东新区

价格:
¥205.9/1ml ¥127.9/100g ¥48.9/25g ¥503.9/500g

联系人:阿拉丁李高志

产品详情:氯菊酯标准溶液


公司名:上海创赛科技有限公司

区域:上海市嘉定区

价格:
¥51.0/25g ¥123.0/100g ¥483.0/500g ¥1847.0/2500g

联系人:夏言

产品详情:[Perfemiker]氯菊酯(顺反异构体混合物),95%


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相关化合物

【氯菊酯】化源网提供氯菊酯CAS号52645-53-1,氯菊酯MSDS及其说明、性质、英文名、生产厂家、作用/用途、分子量、密度、沸点、熔点、结构式等。CAS号查询氯菊酯上化源网,专业又轻松。>>电脑版:氯菊酯

标题:氯菊酯_MSDS_用途_密度_氯菊酯CAS号【52645-53-1】_化源网 地址:https://m.chemsrc.com/mip/cas/52645-53-1_237421.html