塩化ベンジル

危険有害性情報のコード(GHS)

• 絵表示(GHS)

  

• 注意喚起語

  Danger

• 危険有害性情報

  H302：飲み込むと有害

  H315：皮膚刺激

  H317：アレルギー性皮膚反応を起こすおそれ

  H318：重篤な眼の損傷

  H331：吸入すると有毒

  H335：呼吸器への刺激のおそれ

  H350：発がんのおそれ

  H373：長期にわたる、または反復暴露により臓器の障 害のおそれ

• 注意書き

  P280：保護手袋/保護衣/保護眼鏡/保護面を着用するこ と。

  P301+P312：飲み込んだ場合：気分が悪い時は医師に連絡する こと。

  P302+P352：皮膚に付着した場合：多量の水と石鹸で洗うこと。

  P305+P351+P338：眼に入った場合：水で数分間注意深く洗うこと。次にコ ンタクトレンズを着用していて容易に外せる場合は外す こと。その後も洗浄を続けること。

  P308+P313：暴露または暴露の懸念がある場合：医師の診断/手当てを 受けること。

塩化ベンジル 価格

塩化ベンジル 化学特性,用途語,生産方法

• 外観

  無色～わずかにうすい黄色, 澄明の液体

• 性質

  塩化ベンジルは、融点が−39°Cで、沸点が179°Cの無色液体です。刺激臭の強い液体で、眼、皮膚、粘膜を強く刺激します。

  クロロホルムやエーテルなど、多くの有機溶媒に溶解します。ただし水には不溶です。

• 溶解性

  エタノール及びアセトンに極めて溶けやすく、水にほとんど溶けない。

• 解説

  化学式 C6H5CH2Cl 。特有の臭いのある無色の液体。沸点 179℃。トルエンの存在下での光塩素化によって塩化ベンザルとベンゾトリクロリドとともに生成する。加水分解によりベンジルアルコールを生じる。消毒剤の中間体，アミン類のベンジル化剤として使用される。
  ブリタニカ国際大百科事典 小項目事典 ブリタニカ

• 用途

  有機合成、染料及び染料中間体原料

• 用途

  農薬?ゴム薬品原料、染料?医薬中間体原料

• 構造

  塩化ベンジルは、のメチル基にある1つの水素原子が、で置換された構造を有します。化学式はC₇H₇Clで、分子量は126.59であり、密度は1.100です。

• 合成

  

  図2. 塩化ベンジルの合成

  ベンジルアルコールを塩酸で処理して、初めて塩化ベンジルが合成されました。工業的には、トルエンと塩素の気相光化学反応によって、塩化ベンジルを生成可能です。この方法で年間およそ10万トンの塩化ベンジルが生産されています。遊離した塩素原子のフリーラジカルによって反応が進行し、反応の副生成物は塩化ベンザル (英: Benzal chloride) とベンゾトリクロリド (英: Benzotrichloride) などです。

  ブランのクロロメチル化 (英: Blanc chloromethylation) によって、ベンゼンから塩化ベンジルを合成できます。 ブランのクロロメチル化とは、触媒に塩化亜鉛を用いて、芳香族化合物、塩化水素、ホルムアルデヒドから、クロロメチルアレーンを合成する化学反応です。

• 化学的特性

  Benzyl chloride is a colorless to s lightly yellow liquid with a strong, unpleasant, irritating odor. The Odor Threshold is 0.05 ppm.The stabilized form of benzyl chloride contains a fixed amount of a sodium carbonate solution or propylene oxide.
  

• 物理的性質

  Colorless to pale yellowish-brown liquid with a pungent, aromatic, irritating odor. Odor threshold concentration is 47 ppbv (Leonardos et al., 1969). Katz and Talbert (1930) reported an experimental detection odor threshold concentration of 210 μg/m3 (41 ppbv). The solubility of benzyl chloride in water is 0.33 g/L at 4°C, 0.49 g/L at 20°C, and 0.55 g/L at 30°C. It is freely soluble in chloroform, acetone, acetic acid esters, diethyl ether, and ethyl alcohol.

• 使用

  Benzyl chloride is used in the manufacture of benzyl Compounds, dyes, artificial resins, tanning agents, phar maceuticals, plasticizers, synthetic tannins, perfumes, lubricants, and quaternary ammonium compounds. It is also an intermediate in the preparation of phenylacetic acid (precursor to phamaceuticals).

• 調製方法

  Benzyl chloride can be synthesized by chloromethylation of benzene in the presence of a catalyst (ZnCl2) or by treatment of benzyl alcohol with SO2Cl2. Commercially it is produced by chlorination of boiling toluene in the presence of light.

• 主な応用

  Benzyl chloride is used mainly to produce plasticizers (e.g., benzyl butyl phthalate), benzyl alcohol, and phenylacetic acid via benzyl cyanide (used in the production of synthetic penicillin). On a smaller scale, it is used to produce quaternary ammonium salts (for disinfectants and phase-transfer catalysts), benzyl esters (benzyl benzoate and benzyl acetate for the flavors and perfumes industry), dyes of the triphenylmethane series, dibenzyl disulfide (antioxidant for lubricants), benzylphenol, and benzylamines.

• 定義

  ChEBI: Benzyl chloride is a member of the class of benzyl chlorides that is toluene substituted on the alpha-carbon with chlorine.

• 製造方法

  Benzyl chloride is the starting material for a large number of industrial syntheses. The first preparation of it involved not the chlorination of toluene, however, but the reaction of benzyl alcohol with hydrochloric acid (S. Cannizzaro, 1853). Today, most side-chain chlorination of toluene to produce benzyl chloride. Dibenzyl ether is formed as a byproduct in the alkaline hydrolysis of benzyl chloride to benzyl alcohol. This ether can be re-converted to benzyl chloride by cleavage with hydrogen chloride at a temperature below 100°C.

• 反応性

  Benzyl chloride can be oxidized to benzoic acid or benzaldehyde, or substituted to give the halogenated, sulfonated or nitrated product.With NH3 it yields mono-, di- or tribenzyl amine. With alcohols in base the benzylalkyl ether is formed. With phenols either the phenolic or nuclear hydrogens can react to give benzylaryl ether or benzylated phenols. Reaction with NaCN gives benzyl cyanide (phenylacetonitrile); with aliphatic primary amines the product is the N-alkylbenzylamine, and with aromatic primary amines N-benzylaniline is formed. Benzyl chloride is converted to butyl benzyl phthalate plasticizer and other chemicals.

• 一般的な説明

  Benzyl chloride appears as a colorless liquid with an irritating odor. Toxic by inhalation and skin absorption. Flash point 153°F. Slightly soluble in water. Corrosive to metals and tissue. A lachrymator. Density 9.2 lb /gal.

• 空気と水の反応

  A lachrymator. Slightly soluble in water.

• 反応プロフィール

  Halogenated aliphatic compounds, such as Benzyl chloride, are moderately or very reactive. Reactivity generally decreases with increased degree of substitution of halogen for hydrogen atoms. Materials in this group are incompatible with strong oxidizing and reducing agents. Also, they are incompatible with many amines, nitrides, azo/diazo compounds, alkali metals, and epoxides.

• 危険性

  Highly toxic, intense eye and skin irritant. A lachrymator. Upper respiratory tract irritant. Prob- able carcinogen.

• 健康ハザード

  Benzyl chloride is a corrosive liquid. Con tact with the eyes can cause corneal injury.Exposure to its vapors can produce intenseirritation of the eyes, nose, and throat. Highconcentrations may cause lung edema anddepression of the central nervous system.Flury and Zernik (1931) stated that exposureto 16 ppm for 1 minute was intolerable tohumans. The LC50 values for a 2-hour expo sure in mice and rats are 80 and 150 ppm,respectively. The subcutaneous LD50 valuein rats is 1000 mg/kg (NIOSH 1986).
  Benzyl chloride tested positive to thehistidine reversion–Ames test for mutagenic ity. Subcutaneous administration of this com pound in laboratory animals caused tumors atthe site of application.

• 健康への影響

  A concentration of 16 ppm of benzyl chloride in air is reported to be intolerable to humans within 1 min. The compound is a potent lachrymator, strongly irritating to the eyes, nose, and throat and capable of causing lung edema.

• 火災危険

  Benzyl chloride burns but does not ignite readily. Benzyl chloride may ignite combustibles. When heated to decomposition, Benzyl chloride emits toxic and corrosive fumes. Some organic chlorides decompose to yield phosgene. Incompatible with active metals such as copper, aluminum, magnesium, iron, zinc, and tin and keep from strong oxidizing agents. Avoid contact with acids or acid fumes. Keep separate from oxidizing materials. May become unstable at elevated temperatures and pressures; may react with water resulting in some nonviolent release of energy. Polymerizes with evolution of heat and hydrogen chloride when in contact with all common metals except nickel and lead.

• 使用用途

  塩化ベンジルは催涙性が強いため、かつて戦争で催涙ガスとして使用されていました。

  また有機合成で、アルコールやカルボン酸のヒドロキシ基の水素原子を、基に置換するベンジル化剤として利用可能です。アルコール類や類のヒドロキシ基を保護する有力な方法として、さまざまな化合物の合成に活用されています。

  さらに工業的に、香料、医薬品、染料などの材料中間体として用いられています。

• 毒性学

  The acute oral toxicity (LD50) of benzyl chloride in rats is 1231 mg/kg and in mice 1624 mg/kg. The subcutaneous LD50 (in rats) of benzyl chloride in oil solution is 1000 mg/kg. Exposure of rats and mice to benzyl chloride concentrations of 100 –1000 mg/m3 for 2 h caused irritation of the mucous membranes and conjunctivitis, vol. 11. Benzyl chloride is a strong skin-sensitizing agent for guinea pigs . Benzyl chloride acts weakly mutagenic in validated test systems. Subcutaneous injection of weekly doses of 80 mg/kg for 1 year followed by a post-observation period resulted in local sarcomas with lung metastases in rats. The mean induction time was 500 d. After dermal application of benzyl chloride, skin carcinomas were observed in mice.

• 職業ばく露

  Used as an intermediate and as an irritant gas in chemical warfare. In contrast to phenyl halides, benzyl halides are very reactive. Benzyl chloride is used in production of benzal chloride, benzyl alcohol, and benzaldehyde. Industrial usage includes the manufacture of benzyl compounds, cosmetics, dyes, plastics, synthetic tannins, perfumes and resins. It is used in the manufacture of many pharmaceuticals. Suggested uses of benzyl chloride include: the vulcanization of fluororubbers and the benzylation of phenol and its derivatives for the production of possible disinfectants.

• 発がん性

  Benzyl chloride caused genetic mutations and chromosome-damaging effects in a wide variety of in vitro assays; it was not mutagenic in vivo in the mouse micronucleus assay

• 環境運命予測

  Biological. When incubated with raw sewage and raw sewage acclimated with hydrocarbons, benzyl chloride degraded forming nonchlorinated products (Jacobson and Alexander, 1981).
  Chemical/Physical. Anticipated products from the reaction of benzyl chloride with ozone or OH radicals in the atmosphere are chloromethyl phenols, benzaldehyde and chlorine radicals (Cupitt, 1980).
  Slowly hydrolyzes in water forming HCl and benzyl alcohol. The estimated hydrolysis half-life in water at 25 °C and pH 7 is 15 h (Mabey and Mill, 1978). The hydrolysis rate constant for benzyl chloride at pH 7 and 59.2 °C was determined to be 0.0204/min, resulting in a half-life of 34 min (Ellington et al., 1986).
  May polymerize in contact with metals except nickel and lead (NIOSH, 1997).
  When heated to decomposition, hydrogen chloride gas may be released (CHRIS, 1984).

• 輸送方法

  UN1738 Benzyl chloride, Hazard class: 6.1; Labels: 6.1—Poisonous materials, 8—Corrosive material.

• 合成方法

  トルエンと塩素の光塩素化で得られる。

• 純化方法

  Dry it with MgSO4 or CaSO4, or reflux it with fresh Ca turnings, then fractionally distil it under reduced pressure, collecting the middle fraction and storing it over CaH2 or P2O5. It has also been purified by passage through a column of alumina. Alternatively it is dried over MgSO4 and distilled in a vacuum. The middle fraction is degassed by several freeze-thaw cycles and then fractionated in an 'isolated fractionating column' (which has been evacuated and sealed off at ~10-6 mm) over a steam bath. The middle fraction is retained. The final samples are distilled in a vacuum from this sample and again retaining the middle fraction. The purity is >99.9% (no other peaks are visible by GLC, and the NMR spectrum is consistent with the structure. [Mohammed & Kosower J Am Chem Soc 93 1709 1971, Beilstein 5 IV 809.] IRRITANT and strongly LACHRYMATORY.

• 不和合性

  May form explosive mixture with air. Contact with water forms hydrogen chloride fumes. Strong oxidizers may cause fire and explosions. Unstabilized benzyl chloride undergoes polymerization with copper, aluminum, iron, zinc, magnesium, tin, and other common metals except lead and nickel, with the liberation of heat and hydrogen chloride gas. May accumulate static electrical charges, and may cause ignition of its vapors. Attacks some plastics and rubber. Thermal decomposition and polymerization reactions are inhibited, to a limited extent, by addition of triethylamine, propylene oxide, or sodium carbonate.

• 廃棄物の処理

  Incineration @ 816 C for 0.5 second minimum for primary combustion and 1204 C for 12.0 second for secondary combustion. Elemental chlorine formation may be alleviated by injection of steam or methane into the combustion process.

塩化ベンジル 上流と下流の製品情報

塩化ベンジル 生産企業

Global(691)Suppliers

塩化ベンジル スペクトルデータ(¹HNMR、¹³CNMR、ESR、IR1、IR2、MS、Raman)

100-44-7, 塩化ベンジル キーワード