enow.com Web Search

Search results

1. Results from the WOW.Com Content Network

2. 1-Ethyl-3- (3-dimethylaminopropyl)carbodiimide - Wikipedia

   en.wikipedia.org/wiki/1-Ethyl-3-(3-dimethylamino...

   1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC, EDAC or EDCI) is a water-soluble carbodiimide usually handled as the hydrochloride. [1] It is typically employed in the 4.0-6.0 pH range. It is generally used as a carboxyl activating agent for the coupling of primary amines to yield amide bonds.

3. Dimethylethanolamine - Wikipedia

   en.wikipedia.org/wiki/Dimethylethanolamine

   Dimethylethanolamine (DMAE or DMEA) is an organic compound with the formula (CH 3) 2 NCH 2 CH 2 OH. It is bifunctional, containing both a tertiary amine and primary alcohol functional groups. It is a colorless viscous liquid. It is used in skin care products for improving skin tone and also taken orally as a nootropic.

4. Carbodiimide - Wikipedia

   en.wikipedia.org/wiki/Carbodiimide

   The O-acylisourea will react with amines to give the desired amide 3 and urea 4. The possible reactions of the O-acylisourea 2 produce both desired and undesired products. The O-acylisourea 2 can react with an additional carboxylic acid 1 to give an acid anhydride 5, which can react further to give the amide 3.

5. PRL-8-53 - Wikipedia

   en.wikipedia.org/wiki/PRL-8-53

   PRL-8-53 is a nootropic substituted phenethylamine that has been shown to act as a hypermnesic drug in humans; it was first synthesized by medical chemistry professor Nikolaus Hansl at Creighton University in the 1970s as part of his work on amino ethyl meta benzoic acid esters.

6. Ethyl lauroyl arginate - Wikipedia

   en.wikipedia.org/wiki/Ethyl_lauroyl_arginate

   The first synthesis of ethyl lauroyl arginate hydrochloride and its antimicrobial properties were reported in 1976. In the earlies 1980s, LAMIRSA together with Consejo Superior de Investigaciones Científicas (CSIC, Barcelona) began to investigate a new approach to the control of pathogens in food through the application of cationic surfactants based on natural building blocks that inhibit the ...

7. Sign in to AOL Desktop Gold and manage your usernames

   help.aol.com/articles/aol-desktop-signing-on

   3. On the Sign On screen, click the small arrow pointing down to bring up a list of all stored usernames. 4. Select the desired username by clicking on it. Click Continue once you selected the username. 5. Once you click Continue a new window appears. Check if the correct username is displayed and click Continue. 6.