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  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. Aminolysis - Wikipedia

    en.wikipedia.org/wiki/Aminolysis

    In chemistry, aminolysis (/am·i·nol·y·sis/) is any chemical reaction in which a molecule is lysed (split into two parts) by reacting with ammonia (NH 3) or an amine. [1] The case where the reaction involves ammonia may be more specifically referred to as ammonolysis .

  4. EDAC - Wikipedia

    en.wikipedia.org/wiki/Edac

    1 Science and technology. 2 Other uses. 3 See also. Toggle the table of contents. ... 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide, a water-soluble carbodiimide ...

  5. 3T3-L1 - Wikipedia

    en.wikipedia.org/wiki/3T3-L1

    Differentiated adipocytes in a 3T3-L1 cell line stained with Oil Red O. 3T3-L1 is a sub clonal cell line derived from the original 3T3 Swiss albino cell line of 1962. The 3T3 original cell line was isolated from a mouse embryo and propagated for this specific line of 3T3 cells is used to study adipose tissue-related diseases and dysfunctions.

  6. Ethylamine - Wikipedia

    en.wikipedia.org/wiki/Ethylamine

    CH 3 CHO + NH 3 + H 2 → CH 3 CH 2 NH 2 + H 2 O. Ethylamine can be prepared by several other routes, but these are not economical. Ethylene and ammonia combine to give ethylamine in the presence of a sodium amide or related basic catalysts. [5] H 2 C=CH 2 + NH 3 → CH 3 CH 2 NH 2. Hydrogenation of acetonitrile, acetamide, and nitroethane ...

  7. Solvolysis - Wikipedia

    en.wikipedia.org/wiki/Solvolysis

    An example of a solvolysis reaction is the reaction of a triglyceride with a simple alcohol such as methanol or ethanol to give the methyl or ethyl esters of the fatty acid, as well as glycerol. This reaction is more commonly known as a transesterification reaction due to the exchange of the alcohol fragments.

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  9. Thioester - Wikipedia

    en.wikipedia.org/wiki/Thioester

    CH 3 COSK + RX → CH 3 COSR + KX. The analogous alkylation of an acetate salt is rarely practiced. The alkylation can be conducted using Mannich bases and the thiocarboxylic acid: CH 3 COSH + R' 2 NCH 2 OH → CH 3 COSCH 2 NR' 2 + H 2 O. Thioesters can be prepared by condensation of thiols and carboxylic acids in the presence of dehydrating ...