931120-51-3

Basic information

• Product Name: 2,4-bis(docosyloxy)benzyl alcohol
• Synonyms: 2,4-bis(docosyloxy)benzyl alcohol
• CAS NO: 931120-51-3
• Molecular Weight: 757.321
• Mol File: 931120-51-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2,4-bis(docosyloxy)benzyl alcohol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-bis(docosyloxy)benzyl alcohol(931120-51-3)
• EPA Substance Registry System: 2,4-bis(docosyloxy)benzyl alcohol(931120-51-3)

Safety Data

• Hazardous Substances Data: 931120-51-3(Hazardous Substances Data)

Usage

Type of compound

Organic

Class

Alcohols

Structure

Long hydrocarbon chain

Usage

Surfactant and emulsifier

Applications

Industrial and consumer products, cosmetics, personal care products, and pharmaceuticals

Surfactant properties

Lowers surface tension between two substances

Emulsifying properties

Mixes and stabilizes different types of ingredients

Lubricant

Long hydrocarbon chain

Conditioning agent

Long hydrocarbon chain

Upstream product

• 6938-66-5 1-Bromodocosane 
• 931120-55-7 Kb-Gly-Ala-Fmoc 
• 931120-54-6 Kb-Gly-H 
• 931120-53-5 Fmoc-Gly-OKb, Kb=2,4-didocosyloxybenzyl 
• 955095-30-4 2,4-bis(docosyloxy)benzaldehyde 
• 95-01-2 2,4-Dihydroxybenzaldehyde 

Downstream Products

• 1324007-72-8 C₇₉H₁₂₉N₃O₉S 
• 1324007-73-9 C₆₄H₁₁₉N₃O₇S 
• 1324007-64-8 C₇₂H₁₁₆N₂O₇S 
• 955095-18-8 (2,4-bis(docosyloxy)phenyl)methane amine 
• 931120-54-6 Kb-Gly-H 
• 931120-56-8 Kb-Leu-H 
• 931120-58-0 Kb-Leu-Leu-H 
• 931120-55-7 Kb-Gly-Ala-Fmoc 
• 931120-57-9 Kb-Leu-Leu-Fmoc 

Relevant articles and documents

Method for synthesis of peptide using a carrier

Disclosed are a carrier for use for separation purpose and a method for separation of a compound which enable a chemical reaction to be performed in a liquid phase, enable a compound of interest to be separated from the liquid phase after the completion of the reaction readily, enable the separated compound to be evaluated by structural analysis or the like while the compound being bound to the carrier, and enable the compound to be separated from the carrier readily. A carrier for separation which has a reaction site capable of reacting with other compound on a benzene ring, and a long-chain group having a specified carbon atom(s) at each of the ortho-position and the para-position of the reaction site through an oxygen atom.

PRODUCTION METHOD OF OLIGONUCLEOTIDE

The problem of the present invention is provision of a method of producing an n+p-mer oligonucleotide efficiently in a high yield, which includes use of, as a starting material, an n-mer oligonucleotide wherein the 3′-terminal hydroxyl group is protected,

Hydrophobic tag-assisted liquid-phase synthesis of a growth hormone-inhibiting peptide somatostatin

Hydrophobic tag-assisted liquid-phase peptide synthesis technique and disulfide bond formation have been well-combined, leading to the efficient and practical preparation of a growth hormone-inhibiting peptide somatostatin. Intramolecular disulfide bond f