β-カリオフィレン

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

  H304：飲み込んで気道に侵入すると生命に危険のおそ れ

  H317：アレルギー性皮膚反応を起こすおそれ

• 注意書き

  P261：粉じん/煙/ガス/ミスト/蒸気/スプレーの吸入を避ける こと。

  P272：汚染された作業衣は作業場から出さないこと。

  P280：保護手袋/保護衣/保護眼鏡/保護面を着用するこ と。

  P301+P310：飲み込んだ場合：直ちに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。

  P331：無理に吐かせないこと。

β-カリオフィレン 価格

β-カリオフィレン 化学特性,用途語,生産方法

• 外観

  無色～うすい黄色、液体

• 定義

  本品は、次の化学式で表されるセスキテルペン炭化水素である。

• 解説

  (1R-4E-9S)-4,11,11-trimethyl-8-methylenebicyclo[7.2.0]undec-4-ene．C15H24(204.34)．β-カリオフィレンともいう．二環性セスキテルペン．フトモモ科Eugenis caryophyllaのクローブ油のなかにα-カリオフィレンとともに含まれているが，アカマツPinns densifloraやヤマジソMosla japonicaなど，植物界に広く存在している．"沸点129～130 ℃(1.9 kPa)．[α]_D"－9.9°(ベンゼン)．2分子の塩化水素を付加して融点69～70 ℃ の結晶になる．芳香性材料として使われる．α-カリオフィレンはα-フムレンと同じ．
  森北出版「化学辞典（第2版）

• 用途

  有機合成原料。

• 化粧品の成分用途

  皮膚コンディショニング剤、香料

• 化学的特性

  Clear colorless liquid

• 天然物の起源

  Three isomers (α-, β-, and γ-caryophyllene) are found in nature. The β-isomer is the most frequently encountered and most abundant. This sesquiterpene hydrocarbon occurs naturally in approximately 60 essential oils, mainly in that of cloves, from which it was originally isolated. The chemical structure has been thoroughly studied; other studies have been conducted on the isolation and the dipolar moment, as well as on its oxide. Reported found in lime peel oil, lemon, grapefruit, guava fruit, raspberry, black currant, carrot, celery seed, cinnamon bark, anise, nutmeg, cumin seed, ginger, pepper, peppermint oil, mace, laurel and caraway herb.

• 使用

  β-Caryophyllene is notable for having a cyclobutane ring, a rarity in nature. β-Caryophyllene is one of the chemical compounds that contributes to the spiciness of black pepper. β-Caryophyllene was shown to selectively bind to the cannabinoid receptor type-2 (CB2) and to exert significant cannabimimetic antiinflammatory effects in mice.

• 定義

  ChEBI: A beta-caryophyllene in which the stereocentre adjacent to the exocyclic double bond has S configuration while the remaining stereocentre has R configuration. It is the most commonly occurring form of <greek beta-caryophyllene, occurring in many essential oils, particularly oil of cloves.

• 製造方法

  Isolated from oil of clove stems and separated from eugenol by treating the oil with 7% sodium carbonate solution, extracting with ether, repeating the carbonate treatment on the concentrated extracts, and finally steam distilling.

• 一般的な説明

  Pale yellow oily liquid with an odor midway between odor of cloves and turpentine.

• 空気と水の反応

  Insoluble in water.

• 反応プロフィール

  The unsaturated aliphatic hydrocarbons, such as BETA-CARYOPHYLLENE, are generally much more reactive than the alkanes. Strong oxidizers may react vigorously with them. Reducing agents can react exothermically to release gaseous hydrogen. In the presence of various catalysts (such as acids) or initiators, compounds in this class can undergo very exothermic addition polymerization reactions.

• 火災危険

  BETA-CARYOPHYLLENE is combustible.

• 安全性プロファイル

  A skin irritant. Combustible liquid. When heated to decomposition it emits acrid smoke and irritating fumes.

• 発がん性

  Caryophyllene showed significant activity as an inducer of the detoxifying enzyme glutathione S-transferase in the mouse liver and small intestine. The ability of natural anticarcinogens to induce detoxifying enzymes has been found to correlate with their activity in the inhibition of chemical carcinogenesis (253a).

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