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B104256

Sigma-Aldrich

Butyrylthiocholine iodide

98%

Synonym(s):

(2-Mercaptoethyl)trimethylammonium iodide butyrate

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About This Item

Linear Formula:
(CH3)3N(I)CH2CH2SCOCH2CH2CH3
CAS Number:
1866-16-6
Molecular Weight:
317.23
Beilstein:
3729509
EC Number:
217-475-7
MDL number:
MFCD00011845
UNSPSC Code:
12352103

Assay

98%

mp

171-174 °C (lit.)

SMILES string

[I-].CCCC(=O)SCC[N+](C)(C)C

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

InChI key

WEQAAFZDJROSBF-UHFFFAOYSA-M

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Description
Pricing

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Denis Josse et al.
Chemico-biological interactions, 232, 94-100 (2015-03-21)
In this work, our goals were to establish whether hair decontamination by showering one hour post-exposure to the highly toxic organophosphate nerve agent VX was effective, whether it required the addition of a detergent to water and, if it could
Cristobal Narvaez et al.
Chemosphere, 135, 75-82 (2015-04-29)
Inhibition of blood esterase activities by organophosphate (OP) pesticides has been used as a sensitive biomarker in birds. Furthermore, compared to mammalian vertebrates, less is known about the role of these enzyme activities in the digestive tracts of non-mammalian vertebrates
Natalia P Alza et al.
Bioorganic & medicinal chemistry, 22(15), 3838-3849 (2014-07-16)
Alzheimer's disease (AD) is a neurodegenerative disorder associated with memory impairment and cognitive deficit. Most of the drugs currently available for the treatment of AD are acetylcholinesterase (AChE) inhibitors. In a preliminary study, significant AChE inhibition was observed for the
Gabriele Horn et al.
Archives of toxicology, 89(3), 405-414 (2014-06-11)
Organophosphorus compounds (OP) are bound to human butyrylcholinesterase (BChE) and endogenous or exogenous BChE may act as a stoichiometric scavenger. Adequate amounts of BChE are required to minimize toxic OP effects. Simultaneous administration of BChE and oximes may transfer the
Adriana Ferreira Lopes Vilela et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 968, 87-93 (2013-12-11)
The discovery of selective inhibitors for acetylcholinesterase (AChE) or butyrylcholinesterase (BChE) is extremely important for the development of drugs that can be used in the treatment of patients diagnosed with the Alzheimer's disease (AD). For this reason, there is a
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