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
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
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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Signal Word
Danger
Hazard Statements
Precautionary 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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W S Leibel
The Journal of experimental zoology, 247(3), 198-208 (1988-09-01)
The sialated, presumed-globular form of an atypical pseudocholinesterase (pseudo-ChE) previously described from surgeonfish tissues (Leibel: Comparative Biochemistry and Physiology 1988) has been purified to apparent homogeneity using a combination of salt fractionation along with ion-exchange and concanavalin A-Sepharose affinity chromatographic
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.
Kosuke Yamamoto et al.
Planta, 227(4), 809-822 (2007-11-30)
We recently identified plant acetylcholinesterases (E.C.3.1.1.7; AChEs) homologous to the AChE purified from a monocotyledon, maize, that are distinct from the animal AChE family. In this study, we purified, cloned and characterized an AChE from a dicotyledon, siratro. The full-length
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
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
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