L-α-Phosphatidylcholine - ≥15%, from soybean , CAS No.8002-43-5

CAS: 8002-43-5 Cat. No.: L434221 Summenformel: C42H80NO8P Molekulargewicht: 758.06 Beilstein Registry Number: 5209585 EG-Nummer: 232-307-2
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GRADE & PURITY ≥15% from soybean
Synonyms
PC | PC(16:0/18:2(9Z,12Z)) | [(2R)-3-hexadecanoyloxy-2-[(9Z,12Z)-octadeca-9,12-dienoyl]oxypropyl] 2-(trimethylazaniumyl)ethyl phosphate | 1-palmitoyl-2-linoleoyl-phosphatidylcholine | PALMITOYL-LINOLEOYL PHOSPHATIDYLCHOLINE | Soy PC, L-alpha-phosphatidylc
Storage
Store at 2-8°C
Shipped In
Wet ice
★
Size
Deutschland (EU)
USA*
Price
Qty
25g
L434221-25g
—
2 Auf Lager
74,54€
100g
L434221-100g
—
1 Auf Lager
173,46€
500g
L434221-500g
—
3 Auf Lager
347,01€
Enter a quantity for the sizes you want to add.
🧪
Why this grade

≥15%, from soybean for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

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

📚

Literature proof

Cited in 365 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

Product description:

L434221 is a crude extract of soybean phospholipids. Typical lots of purified soybean phosphatidylcholine have fatty acid contents of approximately C16:0 (palmitic), C18:0 (stearic), C18:1(oleic), C18:2 (linoleic), and 18:3 (linolenic) with other fatty acids being minor contributors. Purified phosphatidylcholine is soluble in chloroform and ethanol. Other major phospholipid components include phosphatidylethanolamine and inositol phosphatides. Other phospholipids and neutral lipids such as triglycerides, tocopherols, and sterols may be present. Carbohydrates may also be present. A procedure for determination of the amount of oxidation of egg phosphatidylcholine in a liposome preparation by measurement of the oxidation index has been published. The oxidation index is the ratio of the absorbance at 233 nm to the absorbance at 215 nm. The latter wavelength was chosen since there is little contribution of the fatty acid carbonyl to the absorbance at this wavelength, allowing Beer′s Law to be followed. A method of determining choline content has been published.

Specifications

Synonyme
PC | PC(16:0/18:2(9Z,12Z)) | [(2R)-3-hexadecanoyloxy-2-[(9Z,12Z)-octadeca-9,12-dienoyl]oxypropyl] 2-(trimethylazaniumyl)ethyl phosphate | 1-palmitoyl-2-linoleoyl-phosphatidylcholine | PALMITOYL-LINOLEOYL PHOSPHATIDYLCHOLINE | Soy PC, L-alpha-phosphatidylc
Spezifikationen & Reinheit
≥15%, from soybean
Biochemische und physiologische Mechanismen
Phosphatidylcholine is the major membrane phospholipid in eukaryotic cells. In addition to being the major structural component of cellular membranes, phosphatidylcholine serves as a reservoir for several lipid messengers. It is the source of the bioactiv
Storage
Store at 2-8°C
Verschickt in
Wet ice
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Reinheit
≥15%
Namen und Kennungen
Pubchem Sid
Kanonisches Lächeln
[P](=O)([O-])(OC[C@H](OC(=O)CCCCCCC\C=C/C\C=C/CCCCC)COC(=O)CCCCCCCCCCCCCCC)OCC[N+](C)(C)C
IUPAC Name
[(2R)-3-hexadecanoyloxy-2-[(9Z,12Z)-octadeca-9,12-dienoyl]oxypropyl] 2-(trimethylazaniumyl)ethyl phosphate
InChIKey
JLPULHDHAOZNQI-ZTIMHPMXSA-N
INCHI
1S/C42H80NO8P/c1-6-8-10-12-14-16-18-20-21-23-25-27-29-31-33-35-42(45)51-40(39-50-52(46,47)49-37-36-43(3,4)5)38-48-41(44)34-32-30-28-26-24-22-19-17-15-13-11-9-7-2/h14,16,20-21,40H,6-13,15,17-19,22-39H2,1-5H3/b16-14-,21-20-/t40-/m1/s1
Isomere SMILES
CCCCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCC/C=C\C/C=C\CCCCC
WGK Deutschland
1
RTECS
OG7565000
Alternative CAS-Nummer
55128-59-1
Molekulargewicht
758.06
Beilstein
5209585
Reaxy-Rn
11330961
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=11330961&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
KlasseGlycerophospholipids
SubclassGlycerophosphocholines
Intermediate Tree Nodes Not available
Direct ParentPhosphatidylcholines
Alternative Parents Phosphocholines  Fatty acid esters  Dialkyl phosphates  Dicarboxylic acids and derivatives  Tetraalkylammonium salts  Carboxylic acid esters  Organopnictogen compounds  Organic salts  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  Amines  
Molecular FrameworkAliphatic acyclic compounds
Substituents Diacylglycero-3-phosphocholine - Phosphocholine - Fatty acid ester - Dialkyl phosphate - Dicarboxylic acid or derivatives - Organic phosphoric acid derivative - Phosphoric acid ester - Alkyl phosphate - Fatty acyl - Quaternary ammonium salt - Tetraalkylammonium salt - Carboxylic acid ester - Carboxylic acid derivative - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Amine - Organic salt - Hydrocarbon derivative - Aliphatic acyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as phosphatidylcholines. These are glycerophosphocholines in which the two free -OH are attached to one fatty acid each through an ester linkage.
External Descriptors Diacylglycerophosphocholines
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

5 results found

Lot NumberCertificate TypeDatumArtikel
I2319602Certificate of AnalysisJul 06, 2026 L434221
I2319606Certificate of AnalysisJul 06, 2026 L434221
I2319622Certificate of AnalysisJul 06, 2026 L434221
I2319623Certificate of AnalysisJul 06, 2026 L434221
D2629289Certificate of AnalysisApr 30, 2026 L434221
Chemische und physikalische Eigenschaften
EmpfindlichkeitHygroscopic
Molekulargewicht758.100 g/mol
XLogP312.900
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count8
Rotatable Bond Count40
Exact Mass757.562 Da
Monoisotopic Mass757.562 Da
Topological Polar Surface Area111.000 Ų
Heavy Atom Count52
Formal Charge0
Complexity940.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count2
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds2
Covalently-Bonded Unit Count1
FAQs und Artikel
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Review of the Structural Characteristics, Biological Functions, and Application Advances of Lycopene
Functional Framework of Starch Metabolism-Related Enzymes in Food Science Research and Mechanistic Analysis of Quality Regulation
Mechanistic Analysis of Topical Glutathione in Skincare: Cellular Redox Regulation, Skin Delivery Challenges, and SLN-Based Delivery Strategies
Choline Metabolism and Detection Methods: Pathway Analysis of Choline, Phosphatidylcholine, Betaine, Acetylcholine, and TMAO
Antioxidant Mechanisms, Stability, and Delivery Strategies of Resveratrol in Skincare Research
Antioxidant Mechanisms of Ferulic Acid in Skincare, Vitamin C/E Synergy, and Stable Delivery Applications
Skin Anti-Aging Mechanisms of Carnosine and Decarboxy Carnosine: Active Carbonyl Scavenging, Oxidative-Stress Buffering, and Inhibition of Collagen Glycation Cross-Linking
The Moisturizing and Low-Moisture Protective Mechanisms of Trehalose: From Its α,α-1,1 Structure and Hydration Dynamics to In Vitro Skin Barrier Research
Protective and Potential Reparative Mechanisms of Prinsepia utilis Seed Oil on the Skin Barrier: Fatty Acid Composition, Epidermal Lipid Metabolism, and Research Evidence
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Mechanism of Action of Tranexamic Acid in Pigmentation Care: From the Plasmin System to Regulation of Inflammation-Driven Pro-Melanogenic Signaling
How Palmitoyl Pentapeptide-4 Acts on the Skin: From the KTTKS Sequence and Skin Delivery to Collagen Matrix Responses
How Cyclization Changes Peptide Behavior: Conformational Preorganization, Skin Delivery, and Integrin Binding, Using Cyclopeptide-5 as an Example
The Logic of Biomimetic Peptide Action in Skin: Sequence and Conformation, Skin Delivery, Stability, and Target Matching
How Does Collagen Tripeptide Act on the Skin: Stratum Corneum Delivery, Matrix Protection, and Regulation of Collagen Homeostasis
Potential Mechanisms of p-Cymene in Problem-Prone Skin: Membrane Perturbation, Inflammatory Signaling Modulation, and Localized Delivery
How Coenzyme Q10 Acts on the Skin: Mitochondrial Electron Transfer, Antioxidant Protection of Membrane Lipids, and Lipid-Carrier Delivery
The Combination Logic of Palmitoyl Tripeptide-1 and Palmitoyl Pentapeptide-4: Skin Delivery, Matrix Signaling, and Regulation of Collagen Homeostasis
How Arbutin Regulates Melanin Production: α/β Anomeric Configuration and Tyrosinase Action
Niacinamide Brightening Mechanisms and Formulation Design: Melanosome Transfer, pH Regulation, and Combination Strategies
Why Do Skincare Oligopeptides Have Different Effects? — Molecular Structure, Skin Delivery, and Mechanisms of Action
Citations of This Product
Lösungsrechner
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