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18194-25-7

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  • China Biggest factory Supply High Quality Hydrogenated(lauric acid)Phosphatidylcholine CAS 18194-25-7

    Cas No: 18194-25-7

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18194-25-7 Usage

Description

1,2-DILAUROYL-SN-GLYCERO-3-PHOSPHOCHOLINE, also known as DLPC, is a phospholipid containing the 12 carbon fatty acid/lauric acid (12:0) at the sn-1 and sn-2 positions. It is commonly used in the generation of micelles, liposomes, and other types of artificial membranes. Due to the medium size of the fatty acid chain, DLPC is used to form thinner membranes or lipid bilayers, making it a versatile compound for various applications.

Uses

Used in Pharmaceutical Applications:
1,2-DILAUROYL-SN-GLYCERO-3-PHOSPHOCHOLINE is used as a component in the formation of robust and versatile membrane bilayers for studying the selective and ATP-driven transport of ions across membranes into nanoporous carriers using gramicidin A and ATP synthase.
Used in Cosmetics Industry:
1,2-DILAUROYL-SN-GLYCERO-3-PHOSPHOCHOLINE is used as an ingredient in the creation of micelles, liposomes, and other types of artificial membranes, which are essential for various cosmetic products, such as creams, lotions, and serums, due to their ability to enhance skin hydration and deliver active ingredients.
Used in Research and Development:
1,2-DILAUROYL-SN-GLYCERO-3-PHOSPHOCHOLINE is used as a key component in experimental setups to form thinner membranes than those produced with PC containing the more common long-chain or very long-chain fatty acids, or to simply vary membrane formulation for various research purposes.
Used in Drug Delivery Systems:
1,2-DILAUROYL-SN-GLYCERO-3-PHOSPHOCHOLINE is used as a component in the development of novel drug delivery systems, particularly for enhancing the delivery, bioavailability, and therapeutic outcomes of various pharmaceutical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 18194-25-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,9 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18194-25:
(7*1)+(6*8)+(5*1)+(4*9)+(3*4)+(2*2)+(1*5)=117
117 % 10 = 7
So 18194-25-7 is a valid CAS Registry Number.
InChI:InChI=1/C32H64NO8P.2H2O/c1-6-8-10-12-14-16-18-20-22-24-31(34)38-28-30(29-40-42(36,37)39-27-26-33(3,4)5)41-32(35)25-23-21-19-17-15-13-11-9-7-2;;/h30H,6-29H2,1-5H3;2*1H2/t30-;;/m1../s1

18194-25-7 Well-known Company Product Price

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  • Sigma

  • (P1263)  1,2-Didodecanoyl-sn-glycero-3-phosphocholine  ≥99%, synthetic

  • 18194-25-7

  • P1263-25MG

  • 786.24CNY

  • Detail
  • Sigma

  • (P1263)  1,2-Didodecanoyl-sn-glycero-3-phosphocholine  ≥99%, synthetic

  • 18194-25-7

  • P1263-100MG

  • 2,377.44CNY

  • Detail
  • Sigma

  • (P1263)  1,2-Didodecanoyl-sn-glycero-3-phosphocholine  ≥99%, synthetic

  • 18194-25-7

  • P1263-500MG

  • 9,535.50CNY

  • Detail

18194-25-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dilauroyl-sn-glycero-3-phosphocholine

1.2 Other means of identification

Product number -
Other names 1,2-didodecanoyl-sn-glycero-3-phosphocholine DLPC

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:18194-25-7 SDS

18194-25-7Upstream product

18194-25-7Downstream Products

18194-25-7Relevant articles and documents

Method for producing liposomes with increased percent of compound encapsulated

-

, (2008/06/13)

The efficiency of encapsulating a drug into a liposomal formulation is increased by use of a lipid having a carbon chain containing from about 13 to about 28 carbons during preparation of the liposomes. Preferably the liposomes are multivesicular liposomes.

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