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蒸汽密度
4 (vs air)
蒸汽压
1 mmHg ( 25 °C)
3.3 mmHg ( 37.7 °C)
expl. lim.
37.7 %
折射率
n20/D 1.433 (lit.)
沸点
151-152 °C/755 mmHg (lit.)
密度
1.753 g/mL at 25 °C (lit.)
SMILES字符串
OS(Cl)(=O)=O
InChI
1S/ClHO3S/c1-5(2,3)4/h(H,2,3,4)
InChI key
XTHPWXDJESJLNJ-UHFFFAOYSA-N
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注意
可能含有颗粒,在储存时可能变成淡黄绿色
警示用语:
Danger
危险声明
危险分类
Acute Tox. 1 Inhalation - Eye Dam. 1 - Skin Corr. 1A - STOT SE 3
靶器官
Respiratory system
补充剂危害
储存分类代码
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
Carbohydrate research, 344(16), 2209-2216 (2009-09-08)
Five fractions of lentinan, a beta-(1-->3)-D-glucan bearing beta-(1-->6)-d-glucopyranosyl branches, were treated with chlorosulfonic acid for 90 min at 60 degrees C in pyridine medium to synthesize water-soluble sulfated derivatives having the substitution degree of 1.44-1.76. The (13)C NMR spectra of
International journal of biological macromolecules, 48(4), 607-612 (2011-02-09)
Nine modification conditions were designed to sulfate exopolysaccharides (EPS) produced by Enterobacter cloacae Z0206 by chlorosulfonic acid-pyridine (CSA-Pyr) method according to the orthogonal test and focusing on three affecting factors such as the ratio of CSA to Pyr, reaction temperature
Molecules (Basel, Switzerland), 14(5), 1915-1926 (2009-05-28)
The reaction of 3-mercaptopropylsilica (MPS) and chlorosulfonic acid in chloroform afforded silica bonded S-sulfonic acid (SBSSA), which was used as a catalyst for the room temperature synthesis of quinoxaline derivatives from 1,2-diamino compounds and 1,2-dicarbonyl compounds. The catalyst could be
Carbohydrate research, 338(24), 2863-2870 (2003-12-12)
Six water-insoluble (1-->3)-beta-D-glucan fractions TM8-1 to TM8-6 with weight-average molecular mass Mw ranging from 5.76 to 77.4x10(4) obtained from the sclerotia of Pleurotus tuber-regium were sulfated to produce the water-soluble fractions S-TM8-1 to S-TM8-6 with Mw from 6.0 to 64.8x10(4).
Journal of the American Chemical Society, 131(11), 4031-4041 (2009-02-28)
A detailed study of the scope of a new Pd-catalyzed synthesis of indoles from 1,2-dihaloarenes and o-halobenzene sulfonates and imines is described. The cascade reaction comprises an imine alpha-arylation followed by an intramolecular C-N bond-forming reaction promoted by the same
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