Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

COOH

CH2Br COOH. White crystalline solid, m.p. 50"C, b.p. 208 C. Soluble in water and alcohol. Prepared by the action of dry bromine on dry ethanoic acid in presence of small amounts of red phosphorus. Produces sores upon the skin used in chemical syntheses. See Reformatski reaction. [Pg.68]

Isobutyric acid, dimethylacetic acid, 2-methylpropanoic acid, (CHjjjCH COOH, colourless syrupy liquid with an unpleasant odour b.p. 154°C. Prepared by oxidation of 2-methylpropanol with K2Cr207 and H2SO4. Salts soluble in water. Used in alkaline solution for sweetening gasoline. [Pg.71]

CH3 [CHJb-COOH. M.p. 31 5"C, b.p. 268-270 C. A fatty acid, occurring in wool as the potassium salt, as esters in fusel oil, and as glycerides in cows and goats milk and coconut and palm oils. [Pg.78]

CH3 [CH2l24 COOH. M.p. 88 C. Occurs free in many waxes. [Pg.89]

HiN CHj COOH. Crystallizes in colourless prisms m.p. (decomp.), turning brown... [Pg.193]

C(,Hi3N02, CH3 CH2-CHMe-CHNH2-COOH. Colourless crystals, m.p. 284 C (decomp.). The naturally occurring substance is dextrorotatory. An amino-acid, occurring with leucine as a product of protein hydroly-... [Pg.224]

C12H24O, CH3 [CH,]io COOH. Needles, m.p. 44 C, b.p. 225"C/I00mm. A fatty acid occurring as glycerides in milk, spermaceti, laurel oil, coconut oil, palm oil and other vegetable oils. The metal salts are widely used. [Pg.236]

H2N-CH2 [CH2j3.CH(NH2) COOH. Colourless needles, m.p. 224 C (decomp.), very soluble in water, insoluble in alcohol. L-(-H)-Lysine is one of the basic amino-acids occurring in particularly large quantities in the protamine and histone classes of proteins. It is an essential amino-acid, which cannot be synthesized by the body and must be present in the food for proper growth. It can be manufactured by various fermentation processes or by synthesis. [Pg.244]


See other pages where COOH is mentioned: [Pg.22]    [Pg.22]    [Pg.18]    [Pg.28]    [Pg.29]    [Pg.43]    [Pg.53]    [Pg.63]    [Pg.79]    [Pg.83]    [Pg.99]    [Pg.100]    [Pg.116]    [Pg.116]    [Pg.124]    [Pg.129]    [Pg.129]    [Pg.134]    [Pg.149]    [Pg.160]    [Pg.160]    [Pg.180]    [Pg.191]    [Pg.191]    [Pg.193]    [Pg.207]    [Pg.211]    [Pg.225]    [Pg.225]    [Pg.228]    [Pg.231]    [Pg.233]    [Pg.238]    [Pg.239]    [Pg.247]    [Pg.247]    [Pg.247]    [Pg.255]    [Pg.258]    [Pg.268]    [Pg.285]    [Pg.287]    [Pg.291]   


SEARCH



Acids, -COOH

CH Cl COOH

CH2-CH-COOH

CH3CH COOH

COOH acid group

COOH group,

COOH-terminal sequences

COOH-terminated surfaces

Carboxylic acids COOH group

Cobalt CoOH

Community COOH groups

Controlled COOH functional group

Conversion COOH functional group

CooH gene

EDT-TTF-COOH

Hydrocarbons COOH

Isotope effect COOH)

MWNT-COOH

PKa values of terminal - COOH

PS-COOH

Polystyrene-COOH

Preparation of Ketal Protected -COOH

R-COOH

Replacement of OH in the COOH group by fluorine

THC-COOH

THC-COOH-PFPOH-HFBA derivative

Zr-COOH

© 2024 chempedia.info