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质量水平
方案
97.0-103.0% (T)
表单
crystals
SMILES字符串
CCCCOC(=O)c1ccccc1C(O)=O
InChI
1S/C12H14O4/c1-2-3-8-16-12(15)10-7-5-4-6-9(10)11(13)14/h4-7H,2-3,8H2,1H3,(H,13,14)
InChI key
YZBOVSFWWNVKRJ-UHFFFAOYSA-N
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Danger
危险声明
危险分类
Repr. 1B
储存分类代码
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
Bung-Nyun Kim et al.
Biological psychiatry, 66(10), 958-963 (2009-09-15)
Very few studies have examined the association between attention-deficit/hyperactivity disorder (ADHD) and phthalate exposure in humans. The aim of this study was to investigate the impact of phthalates on symptoms of ADHD in school-age children. A cross-sectional examination of urine
Dorien A M van Dartel et al.
Toxicology letters, 201(2), 143-151 (2011-01-05)
The embryonic stem cell test (EST) has been shown to be a promising in vitro method for the prediction of developmental toxicity. In our previous studies, we demonstrated that the implementation of gene expression analysis in the EST may further
Liangpo Liu et al.
Environment international, 42, 78-83 (2011-04-29)
Phthalates are suspected of having adverse effects on androgen-regulated reproductive development in animals and may be toxic for human sperm. The purposes of our study were to investigate the general exposure of a Chinese reproductive age cohort to these ubiquitous
S H Swan et al.
International journal of andrology, 33(2), 259-269 (2009-11-19)
Foetal exposure to antiandrogens alters androgen-sensitive development in male rodents, resulting in less male-typical behaviour. Foetal phthalate exposure is also associated with male reproductive development in humans, but neurodevelopmental outcomes have seldom been examined in relation to phthalate exposure. To
Ahmed M Osman et al.
Reproductive toxicology (Elmsford, N.Y.), 30(2), 322-332 (2010-06-18)
In search for alternative methods for developmental toxicity testing, we investigated whether embryonic stem cell (ESC) differentiation and its modulation by toxic exposure could be monitored by proteome profiling. We compared the proteomes of mouse ESC, differentiating ESC (DIF) and
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