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Basic Description
| Synonyms | CHOLINE BITARTRATE | 87-67-2 | CHOLINI BITARTRAS | 2-(Hydroxyethyl)trimethylammonium bitartrate | Choline tartrate (1:1) | 2-hydroxyethyl(trimethyl)azanium;2,3,4-trihydroxy-4-oxobutanoate | Cholinebitartrate | Cholinibitatratis | 2-Hydroxy-N,N,N-trimethylethanaminium 3-c |
|---|---|
| Specifications & Purity | 10mM in Water |
| Biochemical and Physiological Mechanisms | Choline bitartrate is known to serve as a dietary supplement. Choline acts as a precursor for acetylcholine synthesis. |
| Storage Temp | Store at -80°C |
| Shipped In |
Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available. |
| Product Description |
Choline bitartrate has been used as one of the components in experimental diets to study the effects on reproductive processes and on bone genes during gestation and lactation. |
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Organic nitrogen compounds
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Class
Organonitrogen compounds
- Subclass Quaternary ammonium salts
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Class
Organonitrogen compounds
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Superclass
Organic nitrogen compounds
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic nitrogen compounds |
| Class | Organonitrogen compounds |
| Subclass | Quaternary ammonium salts |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Cholines |
| Alternative Parents | Dicarboxylic acids and derivatives Tetraalkylammonium salts 1,2-aminoalcohols Primary alcohols Organopnictogen compounds Organic salts Hydrocarbon derivatives |
| Molecular Framework | Not available |
| Substituents | Choline - Dicarboxylic acid or derivatives - Tetraalkylammonium salt - 1,2-aminoalcohol - Alkanolamine - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organic salt - Primary alcohol - Organooxygen compound - Amine - Alcohol - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as cholines. These are organic compounds containing a N,N,N-trimethylethanolammonium cation. |
| External Descriptors | Not available |
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Names and Identifiers
| IUPAC Name | 2-hydroxyethyl(trimethyl)azanium;2,3,4-trihydroxy-4-oxobutanoate |
|---|---|
| INCHI | InChI=1S/C5H14NO.C4H6O6/c1-6(2,3)4-5-7;5-1(3(7)8)2(6)4(9)10/h7H,4-5H2,1-3H3;1-2,5-6H,(H,7,8)(H,9,10)/q+1;/p-1 |
| InChIKey | QWJSAWXRUVVRLH-UHFFFAOYSA-M |
| Smiles | C[N+](C)(C)CCO.C(C(C(=O)[O-])O)(C(=O)O)O |
| Isomeric SMILES | C[N+](C)(C)CCO.C(C(C(=O)[O-])O)(C(=O)O)O |
| WGK Germany | 3 |
| Molecular Weight | 253.25 |
| Reaxy-Rn | 4064889 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4064889&ln= |
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
| Sensitivity | Moisture sensitive |
|---|---|
| Specific Rotation[α] | 17° (C=10,H2O) |
| Melt Point(°C) | 150 °C |
| Molecular Weight | 253.250 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 4 |
| Exact Mass | 253.116 Da |
| Monoisotopic Mass | 253.116 Da |
| Topological Polar Surface Area | 138.000 Ų |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 193.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 2 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 2 |
Citations of This Product
| 1. Xianqi Wang, Jie Wang, Beibei Hu, Yuyue Zhang, Hongzhe Tian. (2024) Rapid determination of organophosphorus insecticides residue in fruit juice by a fluorescence sensor based on carbon quantum dots. JOURNAL OF FOOD COMPOSITION AND ANALYSIS, 136 (106816). |
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