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Key Documents

P2880

Sigma-Aldrich

Propionylthiocholine iodide

≥98%

Synonym(s):

(2-Mercaptoethyl)trimethylammonium iodide propionate

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About This Item

Linear Formula:
C8H18NOSI
CAS Number:
Molecular Weight:
303.20
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

≥98%

form

powder

mp

200-202 °C (lit.)

storage temp.

−20°C

SMILES string

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

InChI

1S/C8H18NOS.HI/c1-5-8(10)11-7-6-9(2,3)4;/h5-7H2,1-4H3;1H/q+1;/p-1

InChI key

BJQIXLJDWWVGAE-UHFFFAOYSA-M

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Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Spontaneous recovery of cholinesterases after organophosphate intoxication: effect of environmental temperature.
P Honkakoski et al.
Bulletin of environmental contamination and toxicology, 40(3), 358-364 (1988-03-01)
Manuela F Frasco et al.
Aquatic toxicology (Amsterdam, Netherlands), 77(4), 412-421 (2006-02-25)
The main purpose of this study was to describe the kinetic properties of the cholinesterase (ChE) enzyme present in the eyes of the prawn Palaemon serratus, an abundant, ecological and commercially relevant species of European coastal environments. The obtained results
Beatrice Gagnaire et al.
Chemosphere, 71(3), 553-560 (2007-11-14)
Anti-cholinesterase insecticides constitute a major portion of modern synthetic pesticides and the assessment of cholinesterase (ChE) inhibition is widely used as a specific biomarker for evaluating the exposure of non-target organisms to these pollutants. However, most studies on this biomarker
R N Guedes et al.
Comparative biochemistry and physiology. Part C, Pharmacology, toxicology & endocrinology, 119(2), 205-210 (1998-07-21)
Acetylcholinesterase (AChE, EC 3.1.1.7) purified from the lesser grain borer (Rhyzopertha dominica) was significantly inhibited by higher concentrations of the substrates acetylthiocholine (ATC), acetyl-(beta-methyl) thiocholine (A beta MTC) and propionylthiocholine (PTC). 2. The efficiency of AChE for hydrolyzing different substrates
S Faye et al.
Clinical chemistry, 32(8), 1477-1480 (1986-08-01)
We have developed a succinyldicholine-based assay for serum cholinesterase (EC 3.1.1.8) to help establish whether patients with suspected sensitivity to drugs of this type have enzyme abnormalities that cannot be detected by conventional laboratory techniques. Although the method discriminates between

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