20820

Butyrylthiocholine iodide

Name: Butyrylthiocholine iodide
Brand: SIAL

puriss., ≥99.0% (AT)

Synonym(s):

(2-Mercaptoethyl)trimethylammonium iodide butyrate

Select a Size

All Photos(1)

About This Item

Linear Formula:

(CH₃)₃N(I)CH₂CH₂SCOCH₂CH₂CH₃

CAS Number:

1866-16-6

Molecular Weight:

317.23

UNSPSC Code:

12352116

NACRES:

NA.22

PubChem Substance ID:

329752039

EC Number:

217-475-7

Beilstein/REAXYS Number:

3729509

MDL number:

MFCD00011845

Product Name

Butyrylthiocholine iodide, puriss., ≥99.0% (AT)

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)

impurities

≤0.2% water

mp

171-174 °C (lit.)
171-174 °C

storage temp.

−20°C

Quality Level

300

Looking for similar products? Visit Product Comparison Guide

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

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Activity and polymorphisms of butyrylcholinesterase in a Polish population.

Jasiecki J

Chemico-Biological Interactions, 259, 70-77 (2016)

Comparison of a commercially available assay system with two reference methods for the determination of plasma cholinesterase variants.

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

Tris-(2,3-Dibromopropyl) Isocyanurate, a New Emerging Pollutant, Impairs Cognition and Provokes Depression-Like Behaviors in Adult Rats.

Ye L

PLoS ONE, 10(10), 1-16 (2015)

Esterase Inhibition and Copper Release from Copper Iodide Dental Adhesives - An In Vitro Study.

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

New amide alkaloids from Delphinium brunonianum.

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

View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service