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Merck
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Key Documents

Altri documenti

P2880

Sigma-Aldrich

Propionylthiocholine iodide

≥98%

Sinonimo/i:

(2-Mercaptoethyl)trimethylammonium iodide propionate

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About This Item

Formula condensata:
C8H18NOSI
Numero CAS:
1866-73-5
Peso molecolare:
303.20
Numero CE:
217-482-5
Numero MDL:
MFCD00011839
Codice UNSPSC:
12352100
ID PubChem:
57654513
NACRES:
NA.22

Livello qualitativo

200

Saggio

≥98%

Forma fisica

powder

Punto di fusione

200-202 °C (lit.)

Temperatura di conservazione

−20°C

Stringa SMILE

[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
BJQIXLJDWWVGAE-UHFFFAOYSA-M

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Categorie correlate

Pittogrammi

CorrosionExclamation mark
GHS05,GHS07

Avvertenze

Danger

Indicazioni di pericolo

H315 - H318 - H335

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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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
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