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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
(CH3)3N(I)CH2CH2SCOCH2CH2CH3
CAS 번호:
Molecular Weight:
317.23
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
EC Number:
217-475-7
Beilstein/REAXYS Number:
3729509
MDL number:
InChI key
WEQAAFZDJROSBF-UHFFFAOYSA-M
InChI
1S/C9H20NOS.HI/c1-5-6-9(11)12-8-7-10(2,3)4;/h5-8H2,1-4H3;1H/q+1;/p-1
SMILES string
[I-].CCCC(=O)SCC[N+](C)(C)C
grade
puriss.
assay
≥99.0% (AT)
Quality Level
storage temp.
−20°C
form
crystalline
impurities
≤0.2% water
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관련 카테고리
Application
S-Butyrylthiocholine iodide has been used as a substrate for butyrylcholinesterase (BChE) or plasma cholinesterase activity assay.
Other Notes
Preferred substrate for the determination of plasma cholinesterase variants
저장 등급
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
M Whittaker et al.
Clinical chemistry, 29(10), 1746-1751 (1983-10-01)
For assaying plasma cholinesterase (EC 3.1.1.8) activity and phenotyping by means of dibucaine inhibition, we have compared a commercially available kit, in which butyrylthiocholine is used as substrate, with two reference methods, one using benzoylcholine and the other propionylthiocholine. With
Activity and polymorphisms of butyrylcholinesterase in a Polish population.
Jasiecki J
Chemico-Biological Interactions, 259, 70-77 (2016)
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Ye L
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Gabriela Fernandes et al.
The journal of adhesive dentistry, 22(3), 265-274 (2020-05-22)
To investigate whether dental adhesives modified with polyacrylic acid copper iodide particles could inhibit esterase activity in vitro and the copper release rate from resin matrices, as well as the correlation between the two variables. Different concentrations of copper iodide
Yuan-Sheng Zou et al.
Fitoterapia, 136, 104186-104186 (2019-06-01)
Five new amide alkaloids, named delamide A-E (1-5), along with five known ones, methyl-N-(3-carboxy-2-methylpropanoyl) anthranilate (6), benzoic acid, 2-[(1-oxodecyl) amino]-methylester (7), puberline (8), benzoic acid, 2-[(4-methoxy-2-methyl-1, 4-dioxobutyl) amino]-methylester (9) and benzoic acid, 2-[(4-methoxy-3-methyl-1, 4-dioxobutyl) amino]-methylester (10) were isolated from the
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