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aniline 音标拼音: ['ænəl,in]

n. 苯胺
a. 苯胺的

苯胺苯胺的

WordNet (r) 3.0 (2006) (WordNet)

aniline
n 1: oily poisonous liquid amine obtained from nitrobenzene and
used to make dyes and plastics and medicines [synonym:
{aniline}, {aniline oil}, {aminobenzine}, {phenylamine}]

The Collaborative International Dictionary of English v.0.48 (gcide)

Aniline \An"i*line\, a.
Made from, or of the nature of, aniline.
[1913 Webster] anilism

Aniline \An"i*line\ (?; 277), n. [See {Anil}.] (Chem.)
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regarded as ammonia in which one hydrogen atom has been
replaced by the radical phenyl.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.
[1913 Webster]

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Aniline - Wikipedia
Aniline (From Portuguese: anil, meaning ' indigo shrub ', and -ine indicating a derived substance) [6] is an organic compound with the formula C6H5NH2 Consisting of a phenyl group (−C6H5) attached to an amino group (−NH2), aniline is the simplest aromatic amine
Aniline | C6H5NH2 | CID 6115 - PubChem
Signs and Symptoms of Acute Aniline Exposure: Signs and symptoms of acute exposure to aniline may be severe and include dyspnea (shortness of breath), respiratory paralysis, cardiac arrhythmias, and cardiovascular collapse
Aniline: Definition, Formula, Structure, and Uses - Chemistry Learner
What is aniline Learn its formula, structure, properties, molar mass, pKa value, preparations, reactions, and applications
Aniline | Aromatic, Synthesis, Dyeing | Britannica
Aniline, an organic base used to make dyes, drugs, explosives, plastics, and photographic and rubber chemicals Aniline was first obtained in 1826 by the destructive distillation of indigo
Aniline: What It Is, Key Uses, and Health Risks - ScienceInsights
Aniline is a widely produced industrial organic chemical used as a foundational material in manufacturing processes for plastics, rubber, and pharmaceuticals While its applications are extensive and economically significant, aniline is also categorized as a toxic substance that poses serious risks to human health
Aniline - Structure, Properties, Preparation, Reactions, Uses
It can undergo various reactions to form several other compounds Some of the common reactions of aniline is mentioned below: Coupling Reactions: Aniline reacts with a diazonium salt in a diazo coupling reaction, and form azo dye (like aminoazobenzene) with water and hydrogen chloride as byproducts C6H5N2+Cl- + C6H5NH2 → C6H5N=NC6H4NH2 + H2O
Aniline (C6H5NH2) properties - Chemical Portal
Aniline (C₆H₅NH₂), systematically named benzenamine, represents the simplest aromatic amine and serves as a fundamental building block in organic chemistry and industrial chemical synthesis
What Is Aniline? Its Chemistry, Uses, and Risks
Aniline is the simplest aromatic amine, a compound where an amino group is directly attached to a six-carbon benzene ring Its chemical formula is C6H5NH2, systematically named benzenamine or phenylamine
ANILINE | CAMEO Chemicals | NOAA
Aniline poisoning is characterized by methemoglobin formation in the blood and resulting cyanosis or blue skin The formation of methemoglobin interferes with the oxygen-carrying capacity of the blood
Aniline - Simple English Wikipedia, the free encyclopedia
Aniline is an important commodity chemical A major use for aniline is the preparation of methylenediamine, which is made from aniline and formaldehyde, and then reacts with phosgene to make methylene diphenyl diisocyanate (MDI), one of the main monomers in polyurethane

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