Lysophosphatidylcholine from Non-GMO Soybean - Nature, ≥80%, ≤20% phosphatidylcholine , CAS No.9008-30-4

CAS: 9008-30-4 Cat. No.: L1455929 Número EC: 232-715-0
Disponible para pedir
GRADE & PURITY Native ? Native grade — protein/biomolecule in its natural (non-recombinant, non-denatured) form. Use when native structure and activity are required. ≥80% ≤20% phosphatidylcholine
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5mg
L1455929-5mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
31,90US$
25mg
L1455929-25mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
119,90US$
100mg
L1455929-100mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
299,90US$
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Why this grade

Nature, ≥80%, ≤20% phosphatidylcholine Native for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Especificaciones y pureza
Nature, ≥80%, ≤20% phosphatidylcholine
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Grado
Native
Pureza
≥80%
Nombres e identificadores
Sonrisas canónicasCC(=O)OCC(COP(=O)([O-])OCC[N+](C)(C)C)O
IUPAC Name[(2R)-3-acetyloxy-2-hydroxypropyl] 2-(trimethylazaniumyl)ethyl phosphate
InChIKeyRYCNUMLMNKHWPZ-SNVBAGLBSA-N
INCHI1S/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
Isómeros SMILES CC(=O)OC[C@H](COP(=O)([O-])OCC[N+](C)(C)C)O
WGK Alemania 3
CAS alternativo 9008-30-4
Términos de entrada MeSH 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=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassLipids and lipid-like molecules
ClaseGlycerophospholipids
SubclassGlycerophosphocholines
Intermediate Tree Nodes Lysophosphatidylcholines
Direct Parent1-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 FrameworkAliphatic 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
DescripciónThis 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
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Preguntas frecuentes y artículos
Citations of This Product
Referencias
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]
Calculadoras de soluciones
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