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经验公式(希尔记法):
C12H14O4
化学文摘社编号:
分子量:
222.24
UNSPSC Code:
85151701
NACRES:
NA.25
PubChem Substance ID:
EC Number:
205-036-2
Beilstein/REAXYS Number:
2051402
MDL number:
signalword
Danger
hcodes
Hazard Classifications
Repr. 1B
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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
Michelle Romero-Franco et al.
Environment international, 37(5), 867-871 (2011-03-25)
Sources of phthalates other than Polyvinyl chloride (PVC) related products are scarcely documented in Mexico. The objective of our study was to explore the association between urinary levels of nine phthalate metabolites and the use of personal care products. Subjects
Mikkel G Mieritz et al.
International journal of andrology, 35(3), 227-235 (2012-05-23)
Pubertal gynaecomastia is a clinical sign of an oestrogen-androgen imbalance, which occurs in 40-60% of adolescent Caucasian boys. In most cases no underlying endocrinopathy can be identified. A recent study reports higher plasma phthalate levels in Turkish boys with pubertal
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
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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