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羟基香茅醛缩醛类化合物的合成及对蚊虫的驱避活性
Synthesis of acetal derivatives of hydroxycitronellal and their repellent activity against mosquitoes

作  者: ; ; ; ; ; (宋杰);

机构地区: 江西农业大学园林与艺术学院

出  处: 《昆虫学报》 2010年第11期1241-1247,共7页

摘  要: 为了寻找新的萜类驱避剂,以羟基香茅醛为原料,合成羟基香茅醛二甲缩醛、羟基香茅醛乙二醇缩醛、羟基香茅醛1,3-丙二醇缩醛和羟基香茅醛1,2-丙二醇缩醛,用红外光谱IR、质谱MS分析其结构,对羟基香茅醛1,2-丙二醇缩醛还进行了1HNMR及13CNMR分析。按国标GB/T13917.9-2009测定了它们对白纹伊蚊Aedesalbopictus、中华按蚊Anopheles sinensis及淡色库蚊Culexpipiens的驱避活性。结果表明:10%(质量分数)羟基香茅醛二甲缩醛和羟基香茅醛1,2-丙二醇缩醛对中华按蚊的驱避时间均达到国标B级;羟基香茅醛1,2-丙二醇缩醛还对其他的蚊虫具有驱避作用,20%(质量分数)羟基香茅醛1,2-丙二醇缩醛对白纹伊蚊的驱避时间超过国标B级;10%(质量分数)羟基香茅醛1,2-丙二醇缩醛对淡色库蚊的驱避时间超过国标A级。这些结果说明它们对不同蚊种驱避活性的差别,为不同场合的驱蚊需要提供了理论基础。 In order to seek novel terpenoid repellent,4 acetal derivatives of hydroxycitronellal,i.e.,hydroxycitronellal dimethyl acetal,hydroxycitronellal 1,2-ethandiol acetal,hydroxycitronellal 1,3-propanediol acetal and hydroxycitronellal 1,2-propanediol acetal,were synthesized in this study.Their structures were characterized using IR and MS,1H NMR,and 13C NMR(for hydroxycitronellal 1,2-propanediol acetal only).Repellencies against Aedes albopictus,Anopheles sinensis and Culex pipiens were examined using the method described in GB/T 13917.9-2009.The results showed that the repellent activity of 10%(mass) solution of both hydroxycitronellal dimethyl acetal and hydroxycitronellal 1,2-propanediol acetal against A.sinensis reached grade B as defined in GB/T 13917.9-2009,and that of a concentrated solution(20% in mass) of hydroxycitronellal 1,2-propanediol acetal against A.sinensis even approached to grade A.Hydroxycitronellal 1,2-propanediol acetal also showed the repellency to other mosquitoes as well:the repellent activity of 20%(mass) solutions against A.albopictus and that of 10%(mass) solutions against C.pipiens exceeded the grades B and A,respectively.These results indicate that the repellent activity difference against different mosquito species offers the theoretical basis for using the repellents in different situations.

关 键 词: 羟基香茅醛 缩醛类化合物 白纹伊蚊 中华按蚊 淡色库蚊 驱避活性

领  域: [生物学]

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