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等级
SAJ first grade
蒸汽密度
>1 (vs air)
蒸汽压
3.3 mmHg ( 20 °C)
方案
≥99.0%
表单
liquid
自燃温度
559 °F
expl. lim.
9.9 %
存货情况
available only in Japan
折射率
n20/D 1.418 (lit.)
沸点
145 °C (lit.)
密度
0.894 g/mL at 25 °C (lit.)
SMILES字符串
CCCCOC(=O)C=C
InChI
1S/C7H12O2/c1-3-5-6-9-7(8)4-2/h4H,2-3,5-6H2,1H3
InChI key
CQEYYJKEWSMYFG-UHFFFAOYSA-N
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警示用语:
Warning
危险分类
Acute Tox. 4 Inhalation - Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
靶器官
Respiratory system
储存分类代码
3 - Flammable liquids
WGK
WGK 1
闪点(°F)
98.6 °F - closed cup
闪点(°C)
37 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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The post-functionalization of poly(3-hexylthiophene) (P3HT) via various synthetic routes is reported. Well-defined and monofunctionalized ω-thiol-terminated P3HT, ω-carboxylic acid-terminated P3HT, ω-acrylate-terminated P3HT, and ω-methacrylate-terminated P3HT are obtained in high yields through a straightforward procedure. From those, different novel P3HT-based graft copolymers
Thomas Junkers et al.
Macromolecular rapid communications, 33(11), 984-990 (2012-05-05)
A novel dithioester control agent [dimethyltetrathioterephtalate (DMTTT)] is presented for the thioketone-mediated radical polymerization (TKMP) of n-butyl acrylate. The rate of polymerization is significantly decreased in the presence of DMTTT indicating formation of dormant radical species. During polymerization, molar masses
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Langmuir : the ACS journal of surfaces and colloids, 29(5), 1356-1369 (2013-01-09)
Thermoresponsive behavior of different kinds of polymersomes was studied using small angle neutron scattering (SANS), transmission electron microscopy (TEM), and proton nuclear magnetic resonance ((1)H NMR). The polymersomes were made of block copolymers containing a 2000 Da polyethylene glycol (PEG)
Li Wang et al.
Organic letters, 13(23), 6137-6139 (2011-11-08)
Pd(II)-catalyzed aromatic C-H bond activation using urea as a directing group was achieved in a p-TsOH/AcOH medium under mild reaction conditions. The direct olefination products of various urea derivatives were produced from aryl urea derivatives and butyl acrylate in moderate
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