ベンジジン 化學(xué)特性,用途語,生産方法
反応性
芳香族アミンの一つ。4,4'-ジアミノビフェニルともいう。ベンジジン は，無色またはやや赤色の結(jié)晶。酸素と光で暗黒色に変化する。冷水には溶けにくく、熱水には溶ける。熱エタノール（エチルアルコール）にはよく溶ける。80℃以上の熱水から再結(jié)晶したものは無水和物、60℃以下からは一水和物を生じる。ニトロベンゼンの還元で得られるヒドラゾベンゼンを無機酸と加熱すると、転位反応（ベンジジン転位）がおこって生成する。染料の原料として使われたが、現(xiàn)在は使用を禁止されている。また種々の金屬イオンの検出試薬、リン酸イオン、硫酸イオンの沈殿試薬としても用いられる。発癌(はつがん)性が強く、粉末でも蒸気でも皮膚から吸収されるので、取扱いには十分注意する必要がある。［務(wù)臺 潔］
解説
biphenyl-4,4′-diamine．C12H12N2(184.24)．ヒドラゾベンゼンを希硫酸と加熱して，ベンジジン転位させてつくられる．結(jié)晶形は3種類あるが，もっとも安定なものは融點128 ℃，沸點400 ℃(98.6 kPa)．無色の鱗片狀結(jié)晶。1845年にロシアのジーニンN.N.Zininがはじめて合成し，62年にドイツのフィティヒR.Fittigがジアミノビフェニル構(gòu)造であることを証明し，74年に同じくドイツのシュルツG.Schultzが2個のアミノ基がともにパラ位にあることを示して構(gòu)造が確定した。ニトロベンゼンを還元してヒドラゾベンゼンにしたのち，これに塩酸または硫酸を作用させてベンジジン転位を起こすことによって作られる。直接染料の重要な中間物であったが，発がん性があることがわかり，製造されなくなった．分析試薬として多くの金屬および非金屬イオンの定性，定量に用いられる．森北出版「化學(xué)辭典（第2版）
説明
Benzidine is a white, greyish-yellow, or slightly reddish crystalline solid or powder. The
major use for benzidine is in the production of dyes, especially azo dyes in the leather, textile,
and paper industries and as a synthetic precursor in the preparation and manufacture
of dyestuffs. It is also used in the manufacture of rubber, as a reagent, and as a stain in
microscopy. It is slightly soluble and slowly changes from a solid to a gas.
化學(xué)的特性
Benzidine is a white, grayish-yellow, or slightly reddish crystalline solid or powder. The
major use for benzidine is in the production of dyes, especially azo dyes in the leather, textile, and paper industries, as a synthetic precursor in the preparation and manufacture of
dyestuffs. It is also used in the manufacture of dyes and rubber, as a reagent, and as a stain
in microscopy. It is slightly soluble and slowly changes from a solid to a gas.
物理的性質(zhì)
Grayish-yellow to pale reddish powder or crystals. Darkens on exposure to air or light. Odorless.
使用
Benzidine was used extensively in the manu facture of dyes. Because of its cancer-causingeffects in humans, its application in dyes hasbeen curtailed. Other uses of this compoundare in chemical analysis: as a reagent for thedetermination of hydrogen peroxide in milkand in the analysis of nicotine. Its hydrochlo ride is used as a reagent to analyze metalsand sulfate.
定義
ChEBI: A member of the class of biphenyls that is 1,1'-biphenyl in which the hydrogen at the para-position of each phenyl group has been replaced by an amino group.
製造方法
1-Nitrobenzene restore 1,2-Diphenylhydrazineturn with acid rearrangement.
調(diào)製方法
Benzidine production is now exclusively for captive consumption and must be carried out in closed systems under stringent workplace controls. Benzidine is used in the synthesisofdyesanddyeintermediates,asahardenerforrubber, and as a laboratory reagent. The rst successful synthetic direct dye was Congo Red, a diazo derivative prepared from benzidinebyBoettigerin1884.Nearlyalldirectdyesareazo products. Congo Red is used in humans intravenously for the medical diagnosis of amyloidosis. The basis for its use is an unexplained afnity for amyloid, which rapidly removes the dye from the blood. It is used medically for the management of profuse capillary hemorrhage such as the one occurring in septicemias and in the terminal phases of leukemia.
一般的な説明
A grayish-yellow to grayish-red, crystalline solid. Toxic by ingestion, inhalation, and skin absorption. Combustion produces toxic oxides of nitrogen. Used to make other chemicals and in chemical and biological analysis.
空気と水の反応
Darkens on exposure to air and light. Soluble in hot water.
反応プロフィール
Benzidine forms insoluble salts with sulfuric acid. Can be diazotized, acetylated and alkylated. Is hypergolic with red fuming nitric acid . Neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides.
危険性
Highly toxic by ingestion, inhalation, and
skin absorption. Confirmed carcinogen.
健康ハザード
Exposure to benzidine causes irritation to the eyes. Laboratory animals exposed to benzidine at as low as 0.01% to 0.08% in food showed adverse health effects, such as organ
weight decrease in the liver, kidney, and body weight, and an increase in spleen weight,
swelling of the liver, and blood in the urine. Exposure may cause an increase in urination, blood in the urine, and urinary tract tumors. Benzidine is considered acutely toxic
to humans by ingestion, with an estimated oral lethal dose of between 50 and 500 mg/kg.
The symptoms of acute ingestion exposure include cyanosis, headache, mental confusion,
nausea, and vertigo. Dermal exposure may cause skin rashes and irritation. Prolonged
exposure to benzidine causes bladder injury in humans
安全性プロファイル
Confirmed human
carcinogen producing bladder tumors.
Experimental carcinogenic and tumorigenic
data. Poison by ingestion and intraperitoneal
routes. Human mutation data reported. Can
cause damage to blood, including hemolysis
and bone marrow depression. On ingestion
causes nausea and vomiting, which may be
followed by liver and kidney damage. Any
exposure is considered extremely hazardous.
When heated to decomposition it emits
highly toxic fumes of NOx. See also
AROMATIC AMINES.
発がん性
Benzidine is known to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in humans.
環(huán)境運命予測
Biological. In activated sludge, <0.1% mineralized to carbon dioxide after 5 d (Freitag et al.,
1985). Kincannon and Lin (1985) reported a half-life of 76 d when benzidine in sludge was
applied to a sandy loam soil.
Soil. Benzidine was added to different soils and incubated in the dark at 23 °C under a carbon
dioxide-free atmosphere. After 1 yr, 8.3 to 11.6% of the added benzidine degraded to carbon
dioxide primarily by microbial metabolism and partially by hydrolysis (Graveel et al., 1986).
Tentatively identified biooxidation compounds using GC/MS include hydroxybenzidine, 3-
hydroxybenzidine, 4-amino-4′-nitrobiphenyl, N,N′-dihydroxybenzidine, 3,3′-dihydroxybenzidine
and 4,4′-dinitrobiphenyl (Baird et al., 1977). Under aerobic conditions, the half-life was estimated
to be 2 to 8 d (Lu et al., 1977).
Chemical/Physical. Benzidine is not subject to hydrolysis (Kollig, 1993). Reacts with HCl
forming a salt (C12H12N22HCl) that is very soluble in water (61.7 mg/L at 25 °C) (Bowman et al.,
1976).
貯蔵
Benzidine should be kept stored in a cool, well-ventilated area, in closed, sealed containers
and out of sunlight and away from heat.
輸送方法
UN1885 Benzidine, Hazard Class: 6.1; Labels:
6.1—Poisonous materials. PGII.
純化方法
Its solution in *benzene is decolorized by percolating through two 2-cm columns of activated alumina, then concentrated until benzidine crystallises on cooling. Recrystallise alternately from EtOH and *benzene to constant absorption spectrum [Carlin et al. J Am Chem Soc 73 1002 1951]. It has also been crystallised from hot water (charcoal) and from diethyl ether. Dry it under vacuum in an Abderhalden pistol. Store it in the dark in a stoppered container. CARCINOGENIC. [Beilstein 13 IV 364.]
不和合性
Dust may form explosive mixture with
air. Incompatible with oxidizers (chlorates, nitrates, peroxides,
permanganates, perchlorates, chlorine, bromine, fluorine,
etc.); contact may cause fires or explosions. On
contact with strong reducing agents, such as hydrides may
form flammable gases. Keep away from alkaline materials,
strong bases, strong acids, oxoacids, epoxides. Contact with
red fuming nitric acid may cause fire. Oxidizes in air.
Neutralizes acids in exothermic reactions to form salts plus
water. May be incompatible with isocyanates, halogenated
organics, peroxides, phenols (acidic), epoxides, anhydrides,
and acid halides.
廃棄物の処理
Incineration; oxides of nitrogen
are removed from the effluent gas by scrubber, catalytic
or thermal device. Package spill residues and
sorbent media in 17 hour epoxy-lined drums and move to
an EPA-approved disposal site. Treatment may include
destruction by potassium permanganate oxidation, hightemperature
incineration, or microwave plasma methods.
398 Benzidine
Encapsulation by organic polyester resin or silicate fixation.
These disposal procedures should be confirmed with
responsible environmental engineering and regulatory
officials.
予防処置
At high temperatures, benzidine breaks down and releases highly poisonous fumes.
During use and handling, workers should wear butyl rubber gloves, goggles, and full
body plastic coveralls and ensure that no skin is exposed.
ベンジジン 上流と下流の製品情報
原材料
準備製品
アシッドレッド114
3,3'-ジアミノベンジジン
4'-[[4,5-ジヒドロ-3-メチル-5-オキソ-1-(4-スルホフェニル)-1H-ピラゾール-4-イル]アゾ]-4-[[4-[[(4-メチルフェニル)スルホニル]オキシ]フェニル]アゾ]-1,1'-ビフェニル-3-スルホン酸二ナトリウム
クロラゾール ブラック E
コンゴーレッド
4,4'-ビス[(2-ヒドロキシ-1-ナフチル)アゾ]-1,1'-ビフェニル-2,2'-ジスルホン酸二ナトリウム
ダイレクト ブルー 6
C. I. Pigment Red 62
5,5'-ジメチル-4,4'-ビス[[2-オキソ-1-[(フェニルアミノ)カルボニル]プロピル]アゾ]-1,1'-ビフェニル-2,2'-ジスルホン酸二ナトリウム
Direct Black BH
4,4'-ビス[(4,5-ジヒドロ-3-メチル-5-オキソ-1-フェニル-1H-ピラゾール-4-イル)アゾ]-1,1'-ビフェニル-2,2'-ジスルホン酸二ナトリウム
3-[[2,2'-ジメチル-4'-[[4-[[(4-メチルフェニル)スルホニル]オキシ]フェニル]アゾ]-1,1'-ビフェニル-4-イル]アゾ]-4-ヒドロキシ-2,7-ナフタレンジスルホン酸二ナトリウム
N,N'-ビスベンジリデンベンジジン
4,4'-ジヨードビフェニル
3,3'-ジニトロベンジジン
4,4'-ビフェニルジカルボニルクロリド
2,7-ジアミノフルオレン
N,N'-[1,1'-ビフェニル-4,4'-ジイルビス(アゾ)ビス(5-ヒドロキシ-7-ソジオスルホナフタレン-6,2-ジイル)]ビス(グリシンナトリウム)
4-アミノ-6-[[4'-[(7-アミノ-1-ヒドロキシ-3-スルホ-2-ナフチル)アゾ]-1,1'-ビフェニル-4-イル]アゾ]-5-ヒドロキシ-3-[(4-ニトロフェニル)アゾ]-2,7-ナフタレンジスルホン酸三ナトリウム
5-アミノ-4-ヒドロキシ-3-[[4'-[(2-ヒドロキシ-1-ナフタレニル)アゾ]-1,1'-ビフェニル-4-イル]アゾ]ナフタレン-2,7-ジスルホン酸二ナトリウム
4-アミノ-3-[(2,5-ジクロロフェニル)アゾ]-6-[[4'-[(3-メチル-4-ヒドロキシフェニル)アゾ]-1,1'-ビフェニル-4-イル]アゾ]-5-ヒドロキシ-2,7-ナフタレンジスルホン酸二ナトリウム