产品名称
Teepol™ 610 S, anionic
form
liquid
manufacturer/tradename
Shell
density
~1.03 g/mL at 20 °C
application(s)
detection
Quality Level
Application
Teepol™ 610 S可用于防止碳捕集技术中酶的动力学研究中的溶液出现表面波纹。
General description
Teepol™ 610 S是一种表面活性剂的混合物,具有很强的润湿和清洁活性。
Legal Information
Teepol is a trademark of Shell Chemical Co.
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
The Journal of hygiene, 85(2), 181-191 (1980-10-01)
In a multi-laboratory trial with the membrane filtration technique, three surfactants--Teepol 610 (T610), Tergitol 7 (T7) and sodium lauryl sulphate (LS)--were compared in media for the enumeration of coliform organisms and Escherichia coli in water. A total of 179 samples
Influence of temperature and solvent concentration on the kinetics of the enzyme carbonic anhydrase in carbon capture technology
Gladis A, et al.
Chemical Engineering Journal, 309, 772-786 (2017)
C M Lawrence et al.
The British journal of dermatology, 116(2), 171-177 (1987-02-01)
Application of 1% potassium hydroxide (KOH) reduced subsequent development of anthralin inflammation without loss of its therapeutic effect on psoriasis. Teepol had a similar but smaller effect on subsequent development of inflammation. The action of KOH appears to have resulted
H T El-Zanfaly
Zentralblatt fur Bakteriologie, Parasitenkunde, Infektionskrankheiten und Hygiene. Zweite naturwissenschaftliche Abteilung: Mikrobiologie der Landwirtschaft der Technologie und des Umweltschutzes, 135(2), 152-157 (1980-01-01)
Tests for susceptibility of three repesentative surface-active agents, incorporated in solid and liquid medium, were carried through with 75 strains of the Streptococcus group. Hyamine 2389 was the most active compound against the tested strains, followed by Teepol 610. Nearly
H Gallati et al.
Journal of clinical chemistry and clinical biochemistry. Zeitschrift fur klinische Chemie und klinische Biochemie, 20(10), 757-760 (1982-10-01)
Catalytic conversion of H2O2 and 2,2'-azino-di(3-ethyl-benzthiazoline-sulphonic acid-(6)) (ABTS) by peroxidase is stopped immediately and completely by the addition of a secondary alkyl sulphate (Teepol-610) or sodium dodecyl hydrogensulphate. The resulting colour intensity of the oxidized ABTS+ is thereby stabilized and
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