Determine the necessary mass, volume, or concentration for preparing a solution.
Nature, ≥80%, ≤20% phosphatidylcholine Native for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Canonical Smiles | CC(=O)OCC(COP(=O)([O-])OCC[N+](C)(C)C)O |
|---|---|
| IUPAC Name | [(2R)-3-acetyloxy-2-hydroxypropyl] 2-(trimethylazaniumyl)ethyl phosphate |
| InChIKey | RYCNUMLMNKHWPZ-SNVBAGLBSA-N |
| INCHI | 1S/C10H22NO7P/c1-9(12)16-7-10(13)8-18-19(14,15)17-6-5-11(2,3)4/h10,13H,5-8H2,1-4H3/t10-/m1/s1 |
| Isomeric SMILES | CC(=O)OC[C@H](COP(=O)([O-])OCC[N+](C)(C)C)O |
| WGK Germany | 3 |
| Alternate CAS | 9008-30-4 |
| MeSH Entry Terms | Lysolecithin;Lysolecithins;Lysophosphatidylcholine;Lysophosphatidylcholines |
| Reaxy-Rn | 28424934 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=28424934&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Glycerophospholipids |
| Subclass | Glycerophosphocholines |
| Intermediate Tree Nodes | Lysophosphatidylcholines |
| Direct Parent | 1-acyl-sn-glycero-3-phosphocholines |
| Alternative Parents | Phosphocholines Dialkyl phosphates Tetraalkylammonium salts Secondary alcohols Carboxylic acid esters Monocarboxylic acids and derivatives Organopnictogen compounds Organic salts Organic oxides Hydrocarbon derivatives Carbonyl compounds Amines |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | 1-acyl-sn-glycero-3-phosphocholine - Phosphocholine - Dialkyl phosphate - Organic phosphoric acid derivative - Phosphoric acid ester - Alkyl phosphate - Tetraalkylammonium salt - Quaternary ammonium salt - Carboxylic acid ester - Secondary alcohol - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Amine - Alcohol - Organic salt - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as 1-acyl-sn-glycero-3-phosphocholines. These are glycerophosphocholines in which the glycerol is esterified with a fatty acid at O-1 position, and linked at position 3 to a phosphocholine. |
| External Descriptors | Monoacylglycerophosphocholines |
| 1. Chenhui Gu, Xuewen Hu, Baixi Shan, Xiaojing Wu, Jun Chen. (2023) Targeted and non-targeted metabolomics uncovering the effects of Er-Miao-Wan formula on rats with hyperuricemia. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, [PMID:36731256] [10.1016/j.jpba.2023.115246] |
| 2. Xiaoyang Sun, Lifen Zhang, Shaojun Tian, Kaizhou Yang, Jianchun Xie. (2019) Phospholipid composition and emulsifying properties of rice bran lecithin from enzymatic degumming. LWT-FOOD SCIENCE AND TECHNOLOGY, [PMID:] [10.1016/j.lwt.2019.108588] |
| 3. Yongxin Li, Wenni Tian, Fang Tian, Yanrong Zhao, Xuguang Zhang, Jie Xiao. (2025) Spatiotemporally programmed co-delivery via double emulsions enables absorption synergy of 5-MTHF-ca and vitamin D3. FOOD RESEARCH INTERNATIONAL, [PMID:40597517] [10.1016/j.foodres.2025.116800] |
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