カルボン

危険有害性情報のコード(GHS)

• 絵表示(GHS)

  

• 注意喚起語

  Warning

• 危険有害性情報

  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。

  P302+P352：皮膚に付着した場合：多量の水と石鹸で洗うこと。

  P321：特別な処置が必要である（このラベルの．．． を見よ）。

  P333+P313：皮膚刺激または発疹が生じた場合：医師の診断/手当てを 受けること。

  P363：汚染された衣類を再使用す場合には洗濯をすること。

  P501：内容物/容器を．．．に廃棄すること。

カルボン 価格

カルボン 化学特性,用途語,生産方法

• 化粧品の成分用途

  香味剤、香料

• 解説

  カルボン．p-メンタン骨格をもつモノテルペンケトン．(＋)-カルボンまたは(S)-カルボンはヒメウイキョウCarum carviの精油に含まれており，(－)-カルボンまたは(R)-カルボンはクロモジLindera umbellataに，また(±)-カルボンはジンジャーグラスzingiber officinalの精油中にそれぞれ含まれている．(＋)-カルボンは，沸点91 ℃(667～800 Pa)．n_D²⁰1.4989．[α]_D＋61.2°．エタノールとは任意の割合でまざり合う．水に難溶．

• 化学的特性

  Carvone occurs as (S)-(+)- carvone ([α]18 D +64.3°,), (R)-()-carvone ([α]20 D 62.5°), or racemic carvone. The optical isomers differ considerably in their sensory properties. They occur in high percentages in a number of essential oils. (+)-Carvone is the main component of caraway oil (about 60%) and dill oil; ()- carvone occurs in spearmint oil at a concentration of 70–80%.
  Both (+)- and ()-carvone are used to flavor a number of foods and beverages. ()-Carvone is produced in much larger quantities and is mainly used in oral hygiene products.

• 物理的性質

  The carvones are colorless to slightly yellow liquids.(+)-Carvone has a herbaceous odor reminiscent of caraway and dill seeds, whereas ()-carvone has a herbaceous odor reminiscent of spearmint. Depending on the reaction conditions, hydrogenation of carvone yields either carveol or dihydrocarvone, which are also used as flavor compounds. When treated with strong acids, carvone isomerizes to carvacrol.

• 天然物の起源

  The optically active and inactive forms have been reported among the constituents of about 70 essential oils. The dextro form is present in carvi, Antheum graveolens, Antheum sowa, Lippia carviodora, Mentha arvensis, etc. The levo form is present in Metha vifidis var. crispa, Mentha longifolia from South Africa, Eucalyptus globules and several mint species. The racemic form is present in ginger grass, Litsea gutalemaleusis, lavender and Artemisia ferganensis. Reported found in citrus oil and juice (lemon, lime, orange), celery seed, anise, clove, coriander seed, calamus, caraway herb and dill seed.

• 使用

  Carvone is useful for the treatment of various metabolic disorders and GI related disorders.

• 定義

  A ketone derived from the terpene dipentene. It is optically active, occurring naturally in both d- and l-forms.

• 製造方法

  In the past, (+)- and ()-carvones were isolated by fractional distillation of caraway oil and spearmint oil, respectively. However, these carvones are now prepared synthetically, the preferred starting materials being (+)- and ()- limonenes, which are converted into the corresponding optically active carvones. Since optical rotation is reversed in the process, (+)-limonene is the startingmaterial for ()-carvone.
  Thepreferred industrialmethod of carvone synthesis utilizes the selective addition of nitrosyl chloride to the endocyclic double bond of limonene. If a lower aliphatic alcohol is used as solvent, limonene nitrosochloride is obtained in high yield. It is converted into carvone oxime by elimination of hydrogen chloride in the presence of a weak base. Acid hydrolysis in the presence of a hydroxylamine acceptor, such as acetone, yields carvone.
  An alternative process for the production of ()-carvone has recently been commercialized. Starting from (+)-limonene 1,2-epoxide, a regioselective rearrangement of the epoxide leads to ()-carveol (trans- :[2102-58-1]; cis- :[2102-59-2]). Thereaction is effected by the use of a catalyst consisting of a combination of metal salts and phenolic compounds.
  ()-Carveol is subsequently oxidized to ()-carvone by anOppenauer oxidation or by dehydrogenation in the presence of special catalysts.The reaction may also be performed as a one-pot reaction.

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