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1133547

USP

Chlorure de choline

United States Pharmacopeia (USP) Reference Standard

Synonyme(s) :

Chlorure de (2-hydroxyéthyl)triméthylammonium

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About This Item

Formule linéaire :
(CH3)3N(Cl)CH2CH2OH
Numéro CAS:
67-48-1
Poids moléculaire :
139.62
Numéro Beilstein :
3563126
Numéro MDL:
MFCD00011721
Code UNSPSC :
41116107
ID de substance PubChem :
329749389
Nomenclature NACRES :
NA.24

Qualité

pharmaceutical primary standard

Fabricant/nom de marque

USP

Pf

302-305 °C (dec.) (lit.)

Application(s)

pharmaceutical (small molecule)

Format

neat

Chaîne SMILES 

[Cl-].C[N+](C)(C)CCO

InChI

1S/C5H14NO.ClH/c1-6(2,3)4-5-7;/h7H,4-5H2,1-3H3;1H/q+1;/p-1

Clé InChI

SGMZJAMFUVOLNK-UHFFFAOYSA-M

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Description générale

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.

Application



  • Extraction of Bioactive Compounds: Choline chloride, combined with sucrose in natural deep eutectic solvents, facilitates the formation of aqueous biphasic systems. These systems are applied in drug extraction processes to improve efficiency and selectivity, particularly in pharmaceutical applications (Ghaffari et al., 2024).


  • Extraction of α-Glucosidase Inhibitors: Utilizing choline chloride-based deep eutectic solvents significantly enhances the selective extraction of α-glucosidase inhibitors from waste seeds. This application is particularly valuable in the development of therapeutic agents for diabetes management, showcasing its versatility in pharmaceutical extraction processes (Liu et al., 2024).


Substrats

Substrat de la choline acétyltransférase

Remarque sur l'analyse

These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.  ​

Autres remarques

USP issued SDS can be found here.
Sales restrictions may apply.

Produit(s) apparenté(s)

Réf. du produit
Description
Tarif

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Xinyin Jiang et al.
Journal of cellular physiology, 229(8), 1016-1027 (2014-03-22)
Maternal choline intake during gestation may influence placental function and fetal health outcomes. Specifically, we previously showed that supplemental choline reduced placental and maternal circulating concentrations of the anti-angiogenic factor, fms-like tyrosine kinase-1 (sFLT1), in pregnant women as well as
Francina Agosti et al.
The European journal of neuroscience, 40(5), 2755-2765 (2014-06-20)
The melanocortin 4 receptor (MC4R) is a G protein-coupled receptor involved in food intake and energy expenditure regulation. MC4R activation modifies neuronal activity but the molecular mechanisms by which this regulation occurs remain unclear. Here, we tested the hypothesis that
O Hemminki et al.
International journal of cancer, 134(12), 2878-2890 (2013-11-20)
At present, it is not possible to reliably identify patients who will benefit from oncolytic virus treatments. Conventional modalities such as computed tomography (CT), which measure tumor size, are unreliable owing to inflammation-induced tumor swelling. We hypothesized that magnetic resonance
Zhuo Li et al.
Biochimica et biophysica acta, 1840(7), 2112-2122 (2014-03-19)
Choline kinase has three isoforms encoded by the genes Chka and Chkb. Inactivation of Chka in mice results in embryonic lethality, whereas Chkb(-/-) mice display neonatal forelimb bone deformations. To understand the mechanisms underlying the bone deformations, we compared the
Shingo Kobayashi et al.
Biochimica et biophysica acta, 1841(9), 1264-1271 (2014-05-17)
In eukaryotic cells, phospholipids are synthesized exclusively in the defined organelles specific for each phospholipid species. To explain the reason for this compartmental specificity in the case of phosphatidylcholine (PC) synthesis, we constructed and characterized a Saccharomyces cerevisiae strain that
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