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80844-07-1生产厂家

80844-07-1价格

80844-07-1

80844-07-1结构式
80844-07-1结构式
  • 常用中文名:依芬普司
  • 常用英文名:Etofenprox
  • CAS号:80844-07-1
  • 分子式:C25H28O3
  • 分子量:376.488
  • 相关类别: 化学农药原药 杀虫剂 拟除虫菊脂杀虫剂
  • 发布时间:2018-09-06 11:09:21
  • 更新时间:2024-01-02 18:16:13
  • 依托芬普利是一种非酯类拟除虫菊酯杀虫剂。依托芬普利对家蝇有毒性(半数致死量=23ng/只)。含有依托芬普利的制剂已用于防治农业害虫。

化源商城直购

中文名 醚菊酯
英文名 etofenprox
中文别名 多来宝
依芬普司
英文别名 TREBON
mti500
ETOPHENPROX
Lenatop
MFCD00210287
1-{[2-(4-Ethoxyphenyl)-2-methylpropoxy]methyl}-3-phenoxybenzene
1-[[2-(4-ethoxyphenyl)-2-methylpropoxy]methyl]-3-phenoxybenzene
a-((p-ethoxy-b,b-dimethylphenethyl)oxy)-m-phenoxytoluene
Ethophenprox
PEPE
Etofenprox
NUKIL
Ethofenprox
PUNKASO
1-((2-(4-Ethoxyphenyl)-2-methylpropoxy)methyl)-3-phenoxybenzene
EINECS 407-980-2
VECTRON
Benzene, 1-[[2-(4-ethoxyphenyl)-2-methylpropoxy]methyl]-3-phenoxy-
2-(4-ethoxyphenyl)-2-methylpropyl 3-phenoxybenzyl ether
描述 依托芬普利是一种非酯类拟除虫菊酯杀虫剂。依托芬普利对家蝇有毒性(半数致死量=23ng/只)。含有依托芬普利的制剂已用于防治农业害虫。
相关类别
密度 1.1±0.1 g/cm3
沸点 481.6±40.0 °C at 760 mmHg
熔点 36ºC
分子式 C25H28O3
分子量 376.488
闪点 165.1±24.6 °C
精确质量 376.203857
PSA 27.69000
LogP 7.34
外观性状 固体
蒸汽压 0.0±1.2 mmHg at 25°C
折射率 1.559
储存条件

库房通风低温干燥0-6°C

稳定性

化学性质稳定,于80℃贮存90d未见明显分解,在pH值2.8~11.9土壤中半衰期约6d。工业品溶点34~35℃。

计算化学

1.疏水参数计算参考值(XlogP):无

2.氢键供体数量:0

3.氢键受体数量:3

4.可旋转化学键数量:9

5.互变异构体数量:无

6.拓扑分子极性表面积27.7

7.重原子数量:28

8.表面电荷:0

9.复杂度:422

10.同位素原子数量:0

11.确定原子立构中心数量:0

12.不确定原子立构中心数量:0

13.确定化学键立构中心数量:0

14.不确定化学键立构中心数量:0

15.共价键单元数量:1

更多

1. 性状:白色晶体

2. 密度(g/mL25 ºC):未确定

3. 相对蒸汽密度(g/mL,空气=1):.157(23℃)。

4. 熔点(ºC):36.4~38

5. 沸点(ºC):208(719.8Pa)、100(3.2×10-2Pa)

6. 沸点(ºC1mmHg):未确定

7. 折射率:未确定

8. 闪点(ºC):未确定

9. 比旋光度(º):未确定

10. 自燃点或引燃温度(ºC):未确定

11. 蒸气压(Pa):32×10-3 (100℃)、8.0×10-3 (25℃),

12. 饱和蒸气压(kPa,60ºC):未确定

13. 燃烧热(KJ/mol):未确定

14. 临界温度(ºC):未确定

15. 临界压力(KPa):未确定

16. 油水(正辛醇/水)分配系数的对数值:11200000

17. 爆炸上限(%,V/V):未确定

18. 爆炸下(%,V/V):未确定

19. 溶解性:氯仿858g/L、丙酮908g/L、醋酸乙酯875g/L、乙醇150g/L、甲醇76.6g/L、二甲苯84.8g/L、水1mg/L

毒理学数据:

口服- 大鼠 LD50: 42800 毫克 / 公斤; 口服- 小鼠 LD50: 107000 毫克/ 公斤

狗>5000mg/kg,LD50 > 1072mg /kg ,雌性>2140mg/kg;雄性小鼠急性经皮LD50 > 1072mg/kg,

CHEMICAL IDENTIFICATION

RTECS NUMBER :
DA0670000
CHEMICAL NAME :
Benzene, 1-((2-(4-ethoxyphenyl)-2-methylpropoxy)methyl)-3-phen oxy-
CAS REGISTRY NUMBER :
80844-07-1
LAST UPDATED :
199701
DATA ITEMS CITED :
18
MOLECULAR FORMULA :
C25-H28-O3
MOLECULAR WEIGHT :
376.53

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
>42800 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JPIFAN Japan Pesticide Information. (Japan Plant Protection Assoc., 1-43-11, Komagome, Toshima-ku, Tokyo 170, Japan) No.1-61, 1969-92. For publisher information, see AGJAEP. Volume(issue)/page/year: (48),23,1986
TYPE OF TEST :
LC50 - Lethal concentration, 50 percent kill
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
>5900 mg/m3/4H
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
NNGADV Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. (Nippon Noyaku Gakkai, 1-43-11, Komagome, Toshima-ku, Tokyo 170, Japan) V.1- 1976- Volume(issue)/page/year: 15,505,1989
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Administration onto the skin
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
>2140 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JPIFAN Japan Pesticide Information. (Japan Plant Protection Assoc., 1-43-11, Komagome, Toshima-ku, Tokyo 170, Japan) No.1-61, 1969-92. For publisher information, see AGJAEP. Volume(issue)/page/year: (48),23,1986
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
>42880 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JPIFAN Japan Pesticide Information. (Japan Plant Protection Assoc., 1-43-11, Komagome, Toshima-ku, Tokyo 170, Japan) No.1-61, 1969-92. For publisher information, see AGJAEP. Volume(issue)/page/year: (48),23,1986
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
>32160 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JPIFAN Japan Pesticide Information. (Japan Plant Protection Assoc., 1-43-11, Komagome, Toshima-ku, Tokyo 170, Japan) No.1-61, 1969-92. For publisher information, see AGJAEP. Volume(issue)/page/year: (48),23,1986
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
>107 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JPIFAN Japan Pesticide Information. (Japan Plant Protection Assoc., 1-43-11, Komagome, Toshima-ku, Tokyo 170, Japan) No.1-61, 1969-92. For publisher information, see AGJAEP. Volume(issue)/page/year: (48),23,1986
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Administration onto the skin
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
>2140 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JPIFAN Japan Pesticide Information. (Japan Plant Protection Assoc., 1-43-11, Komagome, Toshima-ku, Tokyo 170, Japan) No.1-61, 1969-92. For publisher information, see AGJAEP. Volume(issue)/page/year: (48),23,1986
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
>13400 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JPIFAN Japan Pesticide Information. (Japan Plant Protection Assoc., 1-43-11, Komagome, Toshima-ku, Tokyo 170, Japan) No.1-61, 1969-92. For publisher information, see AGJAEP. Volume(issue)/page/year: (48),23,1986
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
>53600 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JPIFAN Japan Pesticide Information. (Japan Plant Protection Assoc., 1-43-11, Komagome, Toshima-ku, Tokyo 170, Japan) No.1-61, 1969-92. For publisher information, see AGJAEP. Volume(issue)/page/year: (48),23,1986
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Mammal - dog
DOSE/DURATION :
>5 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JPIFAN Japan Pesticide Information. (Japan Plant Protection Assoc., 1-43-11, Komagome, Toshima-ku, Tokyo 170, Japan) No.1-61, 1969-92. For publisher information, see AGJAEP. Volume(issue)/page/year: (48),23,1986
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Unreported
SPECIES OBSERVED :
Bird - duck
DOSE/DURATION :
>2 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JPIFAN Japan Pesticide Information. (Japan Plant Protection Assoc., 1-43-11, Komagome, Toshima-ku, Tokyo 170, Japan) No.1-61, 1969-92. For publisher information, see AGJAEP. Volume(issue)/page/year: (48),23,1986 ** OTHER MULTIPLE DOSE TOXICITY DATA **
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
10920 mg/kg/13W-C
TOXIC EFFECTS :
Liver - fatty liver degeneration Liver - changes in liver weight Endocrine - changes in adrenal weight
REFERENCE :
NNGADV Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. (Nippon Noyaku Gakkai, 1-43-11, Komagome, Toshima-ku, Tokyo 170, Japan) V.1- 1976- Volume(issue)/page/year: 14,505,1989
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
226 gm/kg/2Y-C
TOXIC EFFECTS :
Liver - fatty liver degeneration Nutritional and Gross Metabolic - weight loss or decreased weight gain Related to Chronic Data - changes in testicular weight
REFERENCE :
NNGADV Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. (Nippon Noyaku Gakkai, 1-43-11, Komagome, Toshima-ku, Tokyo 170, Japan) V.1- 1976- Volume(issue)/page/year: 14,505,1989
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
180 gm/kg/13W-I
TOXIC EFFECTS :
Liver - changes in liver weight Kidney, Ureter, Bladder - other changes Related to Chronic Data - death
REFERENCE :
NNGADV Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. (Nippon Noyaku Gakkai, 1-43-11, Komagome, Toshima-ku, Tokyo 170, Japan) V.1- 1976- Volume(issue)/page/year: 14,505,1989
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
445 gm/kg/2Y-C
TOXIC EFFECTS :
Liver - changes in liver weight Kidney, Ureter, Bladder - changes in tubules (including acute renal failure, acute tubular necrosis) Related to Chronic Data - death
REFERENCE :
NNGADV Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. (Nippon Noyaku Gakkai, 1-43-11, Komagome, Toshima-ku, Tokyo 170, Japan) V.1- 1976- Volume(issue)/page/year: 14,505,1989
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Mammal - dog
DOSE/DURATION :
124 gm/kg/1Y-C
TOXIC EFFECTS :
Liver - fatty liver degeneration Liver - changes in liver weight Blood - normocytic anemia
REFERENCE :
NNGADV Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. (Nippon Noyaku Gakkai, 1-43-11, Komagome, Toshima-ku, Tokyo 170, Japan) V.1- 1976- Volume(issue)/page/year: 14,505,1989 ** REPRODUCTIVE DATA **
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
DOSE :
3250 mg/kg
SEX/DURATION :
female 6-18 day(s) after conception
TOXIC EFFECTS :
Reproductive - Maternal Effects - other effects Reproductive - Fertility - post-implantation mortality (e.g. dead and/or resorbed implants per total number of implants)
REFERENCE :
NNGADV Nippon Noyaku Gakkaishi. Journal of the Pesticide Science Society of Japan. (Nippon Noyaku Gakkai, 1-43-11, Komagome, Toshima-ku, Tokyo 170, Japan) V.1- 1976- Volume(issue)/page/year: 14,505,1989

符号 GHS09
GHS09
信号词 Warning
危害声明 H362-H410
警示性声明 P201-P260-P263-P273-P308 + P313-P391
个人防护装备 Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
危害码 (欧洲) Xn
危险品运输编码 UN 3077 9 / PGIII
RTECS号 DA0670000

~93%

80844-07-1结构式

80844-07-1

文献:Galin, F. Z.; Rakhimov, R. G.; Tolstikov, G. A. Russian Journal of Organic Chemistry, 1993 , vol. 29, # 1.2 p. 170 Zhurnal Organicheskoi Khimii, 1993 , vol. 29, # 168 p. 202 - 203

~43%

80844-07-1结构式

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文献:Russian Journal of Organic Chemistry, , vol. 38, # 11 p. 1629 - 1634

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80844-07-1结构式

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文献:Russian Journal of Organic Chemistry, , vol. 38, # 11 p. 1629 - 1634

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80844-07-1结构式

80844-07-1

文献:Russian Journal of Organic Chemistry, , vol. 38, # 11 p. 1629 - 1634

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80844-07-1结构式

80844-07-1

文献:Russian Journal of Organic Chemistry, , vol. 38, # 11 p. 1629 - 1634

~%

80844-07-1结构式

80844-07-1

文献:Russian Journal of Organic Chemistry, , vol. 38, # 11 p. 1629 - 1634

制备方法一

异丁酰氯的制备 359.5g异丁酸在室温下(15℃)滴加595g亚硫酰氯,滴毕后升温至75℃,至无氯化氢放出止,收集88~92℃馏分,得293.0g产品。残留物中加入前馏分和新亚硫酰氯100g,常压蒸馏得83~86℃馏分232.3g,88~92℃产品106.1g,共得产品399.1g,含量98.75%,收率91.7%。

1-(4-乙氧基苯基)-2-甲基-1-丙酮的制备将37g苯乙醚与50mL二硫化碳混合,冷却下分批加入无水三氯化铝48g,继续冷却至2~3℃,滴加异丁酰氯32.1g,滴毕再搅拌反应1h。反应液倒入200mL冰水,搅拌下加100mL浓盐酸,分出油层。水层用苯50mL提取3次,苯提取液与油层合并,干燥、脱苯、真空蒸馏得产品2.5g,收率74.4%。

1-(4-乙氧基苯基)-2-溴-2-甲基-1-丙酮的制备将上步产物42g与95mL无水乙醚于20℃、1.5h内滴加8g溴,滴毕继续反应30min,慢慢加入100mL水,搅拌静置分层。醚层经水洗、30%亚硫酸氢钠溶液洗涤,再水洗,干燥,脱醚得白色结晶43g,m.p.36~38℃。

2-(4-乙氧基苯基)-2-甲基丙酸的制备 将上步产物239g、甲醇120mL、原甲酸三乙酯478mL、甲磺酸16mL于60℃保温反应12h,搅拌下加15%氢氧化钠800mL至pH值12,加热回流3h。倾入大烧杯中,加2500mL水、250mLCCl4,静置分层,水层中加浓盐酸250mL,过滤,真空干燥得124g产品,m.p.81~83℃,收率67.7%。

2-(4-乙氧基苯基)-2-甲基丙醇的制备 将上步产物83.5g和500mL乙醚在无水条件下慢慢滴入到450mL乙醚和17g氢化铝锂混合液中,滴毕,于室温下搅拌2h,再滴入乙酸乙酯。滴毕继续反应15min,滴加4mol/L硫酸250mL,分层,醚层用10%氢氧化钠洗涤后再水洗、干燥、放置、脱醚,得产品75g。

醚菊酯的合成将上步产物172g、间苯氧基苄氯207.5g,在氢氧化钠存在下,以四正丁基溴化铵(28.7g)为相转移催化剂,于80℃反应4h,降温后加入390mL水,搅拌20min,甲苯萃取,水洗萃取液,干燥、脱溶、减压蒸馏,收集226~255℃/399.9~633Pa馏分211.5g,含量95.4%,收率63.4%。

制备方法二

对乙氧基苯乙腈在氢氧化钾、水、溴化三甲基苄铵存在下与碘甲烷反应,生成物经水解,然后用氢化铝锂还原,最后在氢化钠和乙腈存在下,与间苯氧基氯苄反应,合成醚菊酯。

制备方法三

叔丁基乙酰苯酯的制备对叔丁基酚(0.67mol)与醋酐(0.8mol)作用,于140℃回流反应4h,脱去副产乙酸和未反应的醋酐,得棕黄色液体,收率95%,含量91.2%。

[4-(2-氯-1,1-二甲基乙基)苯基]乙酸酯的制备将上步产物100g(含量91.2%)与四氯化碳200mL混合物,加热至60℃。加2g偶氮二异丁腈,同时通氯,加流,于1h内通入氯气15g。分析,脱溶得棕红色液体107g,再减压蒸馏,得产品45g,收率89%,含量93.2%。

1-氯-2-(4-乙氧基苯基)-2-甲基丙烷的制备将上步产物100g(含量94%、0.415mol)、硫酸二乙酯160g (1.04mol)、片状氢氧化钾85g(含量82%、1.245mol)混合,搅拌,加热至30℃滴加20%苄基三乙基氯化铵24g(0.0208mol),约10min加完,滴毕升温至40℃,剧烈搅拌反应6h。冷却,加水100mL,搅拌使固体溶解,分层,有机层用水洗涤,减压脱尽低沸物,得黄色液体产物88.5g,含量89.6%,收率89.9%。

醚菊酯的合成将上步产物50g (含量90%、0.21mol)、间苯氧基苯甲醇51.4g(含量98%、0.252mol)、片状氢氧化钾21.5g(含量82%、0.315mol)、二甲基亚砜250mL混合后,在氮气保护下加热至120℃保温10h,减压脱溶,于残液中加入100mL水、100mL苯,搅拌分层,苯层水洗,减压脱苯,得棕黑色黏稠液体94g,高真空蒸馏得醚菊酯49.4g,含量85.6%,收率53.5%。