推荐产品
化驗
98%
mp
147-149 °C (lit.)
SMILES 字串
OC(=O)c1cccc(Oc2ccccc2)c1
InChI
1S/C13H10O3/c14-13(15)10-5-4-8-12(9-10)16-11-6-2-1-3-7-11/h1-9H,(H,14,15)
InChI 密鑰
NXTDJHZGHOFSQG-UHFFFAOYSA-N
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應用
以 3-苯氧基苯甲酸为标准品,采用电子捕获检测-气相色谱法测定尿中 3-苯氧基苯甲酸残留量。也用于合成聚醚酮。
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
Grafting of vapor-grown carbon nanofibers via in-situ polycondensation of 3-phenoxybenzoic acid in poly (phosphoric acid).
Macromolecules, 37(22), 8278-8285 (2004)
Journal of chromatography. B, Biomedical sciences and applications, 695(2), 227-236 (1997-08-01)
The determination of urinary 3-phenoxybenzoic acid enables exposure to pyrethroid insecticides to be evaluated. A method for the quantitative determination of this metabolite in urine is described. The compound and the internal standard (2-phenoxybenzoic acid) are derivatized with pentafluorobenzylbromide and
Environmental science and pollution research international, 26(3), 2987-2997 (2018-12-07)
3-Phenoxybenzoic acid (3-PBA) is a shared metabolite of several synthetic pyrethroid pesticides (SPs) resulting from environmental degradation of parent compounds and thus occurs frequently as a residue in samples. Hence, the importance of 3-PBA evaluation after pyrethroid application. There is
Improved syntheses of poly (oxy-1, 3-phenylenecarbonyl-1, 4-phenylene) and related poly (ether-ketones) using polyphosphoric acid/P 2 O 5 as polymerization medium.
Polymer, 44(15), 4135-4147 (2003)
Environment international, 48, 109-120 (2012-08-16)
Organophosphorus (OP) and pyrethroid (PYR) compounds are the most widely used insecticides. OPs and PYRs are developmental neurotoxicants. Understanding the extent of exposure in the general population and especially in young children is important for the development of public health
商品
Friedel-Crafts acylation with Lewis acid catalysts forms monoacylated products via electrophilic aromatic substitution of arenes.
傅-克酰基化反应是一种芳烃与酰氯或酸酐使用强路易斯酸催化剂的反应。该反应通过亲电芳族取代进行,形成单酰化产物。
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