huile végétale - significado y definición. Qué es huile végétale
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Qué (quién) es huile végétale - definición


Istituto di Genetica Vegetale         
  • Istituto di Genetica Vegetale, Firenze, Italy.
  • Istituto di Genetica Vegetale, Portici, Italy.
Istituto di Genetica Vegetale (IGV) is a research network om Plant Genetics and Breeding within the Italian Consiglio Nazionale delle Ricerche (National Research Council). IGV is headquartered in Bari and has four different Divisions in Portici, Palermo, Florence and Perugia.
Aniline         
  • 2,6-diisopropylaniline]], a colorless liquid when pure, illustrating the tendency of anilines to air-oxidize to dark-colored products.
  • The lone electron pair on the nitrogen delocalizes into the pi system of the benzene ring. This is responsible for nitrogen’s weaker basicity compared to other amines.
  • [[Ball-and-stick model]] of aniline from the [[crystal structure]] at 252 K
  • 400px
  • Aniline can react with bromine even in room temperatures in water. Acetyl chloride is added to prevent tribromination.
  • Cake of [[indigo dye]], which is prepared from aniline.
  • [[Polyaniline]]s can form upon oxidation of aniline.
  • Most aniline is consumed in the production of [[methylenedianiline]], a precursor to polyurethanes.
CHEMICAL COMPOUND
Aminobenzene; Aniline dye; Phenylamine; Aniline dyes; Aniline compounds; Industrial production of aniline; Industrial production of Aniline; Anilinium chloride; Aniline hydrochloride; Anilinium; Amino benzene; Benzamine; C6H5NH2; Coal dye; Coal tar dye; Benzenamine; C.I. 76001; UN 1548; Aniline chloride; Aniline salt; Benzenamine hydrochloride; Phenylamine hydrochloride; Phenylammonium chloride; C6H8ClN; Phenyl amine; Anilene; Benzidam
·adj Made from, or of the nature of, aniline.
II. Aniline ·noun An organic base belonging to the phenylamines. It may be regarded as ammonia in which one hydrogen atom has been replaced by the radical phenyl. It is a colorless, oily liquid, originally obtained from indigo by distillation, but now largely manufactured from coal tar or nitrobenzene as a base from which many brilliant dyes are made.
Phenylamine         
  • 2,6-diisopropylaniline]], a colorless liquid when pure, illustrating the tendency of anilines to air-oxidize to dark-colored products.
  • The lone electron pair on the nitrogen delocalizes into the pi system of the benzene ring. This is responsible for nitrogen’s weaker basicity compared to other amines.
  • [[Ball-and-stick model]] of aniline from the [[crystal structure]] at 252 K
  • 400px
  • Aniline can react with bromine even in room temperatures in water. Acetyl chloride is added to prevent tribromination.
  • Cake of [[indigo dye]], which is prepared from aniline.
  • [[Polyaniline]]s can form upon oxidation of aniline.
  • Most aniline is consumed in the production of [[methylenedianiline]], a precursor to polyurethanes.
CHEMICAL COMPOUND
Aminobenzene; Aniline dye; Phenylamine; Aniline dyes; Aniline compounds; Industrial production of aniline; Industrial production of Aniline; Anilinium chloride; Aniline hydrochloride; Anilinium; Amino benzene; Benzamine; C6H5NH2; Coal dye; Coal tar dye; Benzenamine; C.I. 76001; UN 1548; Aniline chloride; Aniline salt; Benzenamine hydrochloride; Phenylamine hydrochloride; Phenylammonium chloride; C6H8ClN; Phenyl amine; Anilene; Benzidam
·noun Any one of certain class of organic bases regarded as formed from ammonia by the substitution of phenyl for hydrogen.