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吡丙醚

吡丙醚(Pyriproxyfen,95737-68-1)是一种芳族醚,由丙二醇组成,丙二醇在O-1位置具有2-吡啶基,在O-3位置具有4-苯氧基苯基。吡丙醚是一种芳香族醚,是吡啶的成员。吡丙醚衍生自4-苯氧基苯酚。
货品编码 规格 纯度 价格 (¥) 现价(¥) 特价(¥) 库存描述 数量 总计 (¥)
YZM000794-5g 5g 99.74% ¥ 607.00 ¥ 607.00 2-3天
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¥ 0.00
YZM000794-500mg 500mg 99.74% ¥ 487.50 ¥ 487.50 2-3天
- +
¥ 0.00
HCC342946-250mg 250mg 97% ¥ 665.00 ¥ 665.00 4-7周
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¥ 0.00
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中文别名 吡丙醚(95737-68-1),蚊蝇醚,灭幼宝,S31183,S 31183,S-31183
英文别名 Pyriproxyfen(95737-68-1),S31183,S 31183,S-31183,2-[1-Methyl-2-(4-phenoxyphenoxy)ethoxy]pyridine
CAS号 95737-68-1
SMILES CC(COc1ccc(cc1)Oc2ccccc2)Oc3ccccn3
Inchi InChI=1S/C20H19NO3/c1-16(23-20-9-5-6-14-21-20)15-22-17-10-12-19(13-11-17)24-18-7-3-2-4-8-18/h2-14,16H,15H2,1H3
InchiKey NHDHVHZZCFYRSB-UHFFFAOYSA-N
分子式 Molecular Weight C20H19NO3
分子量 Formula 321.37
闪点 FP 165.4±16.2 °C
熔点 Melting point 46-50°C
沸点 Boiling point 462.0±35.0 °C at 760 mmHg
Polarizability极化度 36.8±0.5 10-24cm3
密度 Density 1.2±0.1 g/cm3
蒸汽压 Vapor Pressure 0.0±1.1 mmHg at 25°C
溶解度Solubility Chloroform (Slightly), Methanol (Slightly)
性状 WHITE POWDER OR GRANULES
储藏条件 Storage conditions Refrigerator
吡丙醚(Pyriproxyfen,95737-68-1)毒理性质:
动物 测试类型 途径 实验摄入量 (标准摄入量) 影响 文献来源
rat LD50 oral > 5gm/kg (5000mg/kg)   Pesticide Manual. Vol. 9, Pg. 745, 1991.
rat LD50 skin > 2gm/kg (2000mg/kg)   Pesticide Manual. Vol. 9, Pg. 745, 1991.

吡丙醚(Pyriproxyfen,95737-68-1)物性值单位温度(°C)来源
熔点46℃EXP
log P(辛醇-水)5.550(无)EST
蒸气压2.18E-06 mm Hg 20 EXP
大气OH速率常数5.22E-11 cm3 /分子-秒25 EST
实验注意事项:
1.实验前需戴好防护眼镜,穿戴防护服和口罩,佩戴手套,避免与皮肤接触。
2.实验过程中如遇到有毒或者刺激性物质及有害物质产生,必要时实验操作需要手套箱内完成以免对实验人员造成伤害
3.实验后产生的废弃物需分类存储,并交于专业生物废气物处理公司处理,以免造成环境污染Experimental considerations:
1. Wear protective glasses, protective clothing and masks, gloves, and avoid contact with the skin during the experiment.
2. The waste generated after the experiment needs to be stored separately, and handed over to a professional biological waste gas treatment company to avoid environmental pollution.
Tag:吡丙醚蒸汽压,吡丙醚合成,吡丙醚标准,吡丙醚应用,吡丙醚合成,吡丙醚沸点,吡丙醚闪点,吡丙醚用途,吡丙醚溶解度,吡丙醚价格,吡丙醚作用,吡丙醚结构式,吡丙醚用处,吡丙醚毒理性质
产品说明 吡丙醚(Pyriproxyfen,95737-68-1)是昆虫生长调节剂,吡丙醚溶解度,msds详见主页。
Introduction吡丙醚(Pyriproxyfen,95737-68-1) is An insect growth regulator.
Application1Juvenile hormone analog and insect growth regulator used to control insects by disrupting metamorphosis. Has been effective in controlling mosquito larvae.
Application2Pyriproxyfen is an aromatic ether and a member of pyridines. It derives from a 4-phenoxyphenol.
Application3Pyriproxyfen has a role as a juvenile hormone mimic.
警示图
危险性 warning
危险性警示 Not available
安全声明 H303+H313+H333
安全防护 P264+P280+P305+P351+P338+P337+P313
备注 实验过程中防止吸入、食入,做好安全防护
Safe distance, safe patients! Therapeutic management of oncological patients affected by cutaneous and mucosal adverse events during the COVID-19 pandemic: an Italian experience Supportive care in can
Identifying and managing osteoporosis before and after COVID-19: rise of the remote consultation? Osteoporosis international : a journal established as result of cooperation between the European Found
A Randomized Trial of Hydroxychloroquine as Postexposure Prophylaxis for Covid-19 The New England journal of medicine 2020-08-06
Lions Quest Skills for Adolescence implementation during COVID-19 challenges in Croatia Psychological trauma : theory, research, practice and policy 2020-08-01
[COVID-19: Variable symptoms in mild course: olfactory loss and increased resting heart rate] Deutsche medizinische Wochenschrift (1946) 2020-07-01
1.Pyriproxyfen cyclodextrin inclusion compounds    Journal of Inclusion Phenomena and Macrocyclic Chemistry    2015
Abstract:
Pyriproxyfen is a pyridine based pesticide which is effective against mosquito larvae. Here we report the inclusion complexes (ICs) between guest pyriproxyfen and host β and γ cyclodextrins, but not with α cyclodextrin, based on WAXD, DSC, FTIR, and TGA characterization results . We show that one pyriproxyfen molecule is covered with between one and two β or γ cyclodextrin molecules when it forms columnar ICs upon precipitation from aqueous solution.
2.Sterilising effects of pyriproxyfen on Anopheles arabiensis and its potential use in malaria control/Caroline Harris, Dickson W Lwetoijera, Stefan Dongus, Nancy S Matowo, Lena M Lorenz, Gregor J Devine & Silas Majambere/Parasites & Vectors volume 6, Article number: 144 (2013)
Abstract:
(1)Background
Insecticide resistance poses a major threat to current vector control campaigns. Insecticides with novel modes of action are therefore in high demand. Pyriproxyfen (PPF), a conventional mosquito pupacide, has a unique mode of action that also sterilises adult mosquitoes (unable to produce viable offspring) upon direct contact. However, the timing of PPF exposure in relation to when mosquitoes take a blood meal has an important impact on that sterilisation. This study investigated the relationship between different blood feeding and PPF exposure timings to determine the potential of PPF sterilisation in controlling Anopheles arabiensis.
(2)Methods
Four treatment regimens were investigated: blood fed three days before PPF exposure (A), blood fed one day before PPF exposure (B), blood fed one day after PPF exposure (C) and blood fed three days after PPF exposure (D) for their impact on egg laying (fecundity) and the production of viable offspring (fertility), while the impact of PPF exposure on mosquito survival was investigated in the absence of a blood meal. All regimens and the survival study exposed mosquitoes to PPF via the bottle assay at 3 mg AI/m2 for 30 minutes.
(3)Results
Female mosquitoes that blood-fed one day prior to PPF exposure (regimen B), produced no viable offspring during that gonotrophic cycle (100% reduction in fertility). All other treatments had no significant effect. The observed reductions in fecundity and fertility were caused by the retention of eggs (97% of eggs retained, ie produced in the ovaries but not laid, in regimen B, p = 0.0004). Some of these retained eggs were deformed in shape. PPF exposure on mosquito survival in the absence of a blood meal was found to have no effect.
(4)Conclusions
The results presented here suggest that sterilising adult malaria vectors using PPF could form part of a malaria control strategy, taking advantage of the lack of reported resistance to PPF in mosquitoes and its unique mode of action. We propose that targeting resting mosquitoes, which are highly susceptible to PPF at low doses, is the optimal direction for developing this control tool.
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