P2880
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
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
217-482-5
MDL number:
Assay:
≥98%
Form:
powder
InChI key
BJQIXLJDWWVGAE-UHFFFAOYSA-M
InChI
1S/C8H18NOS.HI/c1-5-8(10)11-7-6-9(2,3)4;/h5-7H2,1-4H3;1H/q+1;/p-1
SMILES string
[I-].CCC(=O)SCC[N+](C)(C)C
assay
≥98%
form
powder
mp
200-202 °C (lit.)
storage temp.
−20°C
Quality Level
Related Categories
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
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J M Monserrat et al.
Comparative biochemistry and physiology. Part C, Pharmacology, toxicology & endocrinology, 120(2), 193-199 (1998-11-25)
In this study, some kinetic and toxicological parameters of the thoracic ganglia cholinesterase from the estuarine crab Chasmagnathus granulata were determined. Effects of the type and concentration of substrate, pH (6.80-8.50), incubation temperature (5-35 degrees C) and eserine on the
Patricia G Rodrigues et al.
American journal of physiology. Heart and circulatory physiology, 316(3), H459-H475 (2018-12-12)
Several studies have demonstrated that administration of doxorubicin (DOXO) results in cardiotoxicity, which eventually progresses to dilated cardiomyopathy. The present work aimed to evaluate the early myocardial changes of DOXO-induced cardiotoxicity. Male New Zealand White rabbits were injected intravenously with
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;
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
Magda A Mohamed et al.
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP, 146(3), 314-324 (2007-05-29)
Acetylcholinesterases (AChEs) have been estimated in the infective juveniles (IJs) of eight different strains of heterorhabditid nematodes. The enzyme content ranged from 45.6 to 421.3 units/10(5) IJs with specific activity 34.0 to 82.6 units/mg protein. The isoenzyme patterns revealed the
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