Skip to Content
Merck
All Photos(1)

Key Documents

More Documents

P2880

Sigma-Aldrich

Propionylthiocholine iodide

≥98%

Synonym(s):

(2-Mercaptoethyl)trimethylammonium iodide propionate

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
C8H18NOSI
CAS Number:
1866-73-5
Molecular Weight:
303.20
EC Number:
217-482-5
MDL number:
MFCD00011839
UNSPSC Code:
12352100
PubChem Substance ID:
57654513
NACRES:
NA.22

Quality Level

200

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

Looking for similar products? Visit Product Comparison Guide

Related Categories

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H315 - H318 - H335

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

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
Andrea Mosca et al.
Clinical chemistry and laboratory medicine, 41(3), 317-322 (2003-04-23)
No comparative information is available concerning the ability of various cholinesterase (ChE) methods to identify succinyldicholine-sensitive patients, purely on the basis of the enzyme activity recorded in serum. Here, we evaluated six different methods for the measurement of ChE activity;
Andreea Ticu Boeck et al.
Biochemical pharmacology, 63(12), 2101-2110 (2002-07-12)
The rat is the model animal for toxicity studies. Butyrylcholinesterase (BChE), being sensitive to inhibition by some organophosphorus and carbamate pesticides, is a biomarker of toxic exposure. The goal of this work was to characterize the purified rat BChE enzyme.
J Trancard et al.
Brain research, 476(2), 213-219 (1989-01-09)
The cholinesterase equipment of cerebral microvessels was studied in some rodents and carnivores using the Koelle-Friedenwald histochemical method with 3 artificial substrates and specific inhibitors for butyrylcholinesterase or acetylcholinesterase. Our observations reveal a great heterogeneity in cholinesterase types and their
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
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