This is a demo store. No orders will be fulfilled.

1,2-dioctanoyl-sn-glycero-3-phosphocholine - >99%, high purity , CAS No.19191-91-4

    Grade & Purity:
  • ≥99%
In stock
Item Number
D130411
Grouped product items
SKU Size
Availability
Price Qty
D130411-25mg
25mg
2
$199.90
D130411-100mg
100mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$549.90

Basic Description

Synonyms PC(8:0/8:0) | Dicapryloyl-L-alpha-lecithin | Q27105079 | 08:0 PC, 1,2-dioctanoyl-sn-glycero-3-phosphocholine, powder | (2-{[(2R)-2,3-bis(octanoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium | 3,5,9-Trioxa-4-phosphaheptadecan-1-aminium, 4-hydroxy-N,N,
Specifications & Purity ≥99%
Biochemical and Physiological Mechanisms Phosphatidylcholine (PC) can form a hydrophobic surface in the mucus by acting as a surfactant to inhibit the penetrance of bacteria.
Storage Temp Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

general description:

Phosphatidylcholine (PC) is one of the most important constituent of the mucosal layer of the colon. 08:0 PC (1,2-dioctanoyl-sn-glycero-3-phosphocholine/C8PC) is a water soluble short alkyl chain lipid.

The list of Phosphatidylcholine products offered by Avanti is designed to provide compounds having a variety of physical properties. Products available include short chain (C3-C8 are water soluble and hygroscopic), saturated, multi-unsaturated and mixed acid PC′s. All of the products are purified by HPLC, and special precautions are taken to protect the products for oxidization and hydrolysis.


application:

08:0 PC (1,2-dioctanoyl-sn-glycero-3-phosphocholine/C8PC) has been used as a substrate to study the analytical capabilities of several methods to determine water soluble phospholipids containing choline (wCh-PL) and also to study the behavior of the its analytical signal in a synthetic serum matrix (data-Trol). It may also be used as a bicellar model to study their phase behavior and to form a lipid film to study its effect on P-glycoprotein′s (P-gp′s) activity/to compare its effect with TWEEN®80 and Cremophor®EL.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Lipids and lipid-like molecules
Class Glycerophospholipids
Subclass Glycerophosphocholines
Intermediate Tree Nodes Not available
Direct Parent Phosphatidylcholines
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 Framework Aliphatic 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
Description This 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

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name [(2R)-2,3-di(octanoyloxy)propyl] 2-(trimethylazaniumyl)ethyl phosphate
INCHI InChI=1S/C24H48NO8P/c1-6-8-10-12-14-16-23(26)30-20-22(33-24(27)17-15-13-11-9-7-2)21-32-34(28,29)31-19-18-25(3,4)5/h22H,6-21H2,1-5H3/t22-/m1/s1
InChIKey YHIXRNNWDBPKPW-JOCHJYFZSA-N
Smiles CCCCCCCC(=O)OCC(COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCC
Isomeric SMILES CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCC
Molecular Weight 509.614
Reaxy-Rn 1917680
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1917680&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

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.

4 results found

Lot Number Certificate Type Date Item
K2212181 Certificate of Analysis Aug 17, 2023 D130411
K2212190 Certificate of Analysis Aug 17, 2023 D130411
F1606061 Certificate of Analysis Jul 14, 2023 D130411
G2218022 Certificate of Analysis May 09, 2023 D130411

Chemical and Physical Properties

Molecular Weight 509.600 g/mol
XLogP3 4.800
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 8
Rotatable Bond Count 24
Exact Mass 509.312 Da
Monoisotopic Mass 509.312 Da
Topological Polar Surface Area 111.000 Ų
Heavy Atom Count 34
Formal Charge 0
Complexity 586.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 1
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Solution Calculators

Reviews

Customer Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.