ボルネオール(464-45-9)

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ボルネオール 製品概要
化学名:ボルネオール
英語化学名:L(-)-Borneol
别名:L(-)-Borneol, 97% 100GR;(-)-Borneol, 97+%;Bornencamphor;Borneol, (1S,2R,4S)-(-)-;endo-2-Hy-droxycamphane;l-2-Bornanol;l-2-Camphanol;Malayancam-phor
CAS番号:464-45-9
分子式:C10H18O
分子量:154.25
EINECS:207-353-1
カテゴリ情報:Miscellaneous Natural Products;Bicyclic Monoterpenes;Biochemistry;Terpenes
Mol File:464-45-9.mol
ボルネオール
ボルネオール 物理性質
融点 206-209 °C
沸点 210 °C(lit.)
比旋光度 -36.2 º (c=5, C2H5OH)
比重(密度) 0.8389 (rough estimate)
蒸気密度5.31 (vs air)
蒸気圧33.5 mm Hg ( 25 °C)
FEMA 2157 | BORNEOL
屈折率 -36 ° (C=5, EtOH)
闪点 150 °F
貯蔵温度 Store below +30°C.
溶解性almost transparency in EtOH
酸解離定数(Pka)15.36±0.60(Predicted)
外見 Crystalline Powder or Crystals
White to light yellow
臭い (Odor)at 10.00 % in dipropylene glycol. pine woody camphor
においのタイプbalsamic
光学活性 (optical activity)[α]20/D 35.3°, c = 5 in ethanol
水溶解度 INSOLUBLE
Merck 14,1338
BRN 3587558
LogP2.75 at 20℃
CAS データベース464-45-9(CAS DataBase Reference)
NISTの化学物質情報Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, (1S-endo)-(464-45-9)
EPAの化学物質情報(-)-Borneol (464-45-9)
安全性情報
主な危険性 F,Xi
Rフレーズ 11-43
Sフレーズ 16-36/37
RIDADR UN 1312 4.1/PG 3
WGK Germany 2
RTECS 番号DT5095000
TSCA Yes
国連危険物分類 4.1
容器等級 III
HSコード 29061900
毒性LD50 orally in Rabbit: 5800 mg/kg
MSDS Information
ProviderLanguage
endo-(1S)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol English
SigmaAldrich English
ACROS English
ALFA English
ボルネオール Usage And Synthesis
外観白色~ほとんど白色, 結晶性粉末~粉末
溶解性エタノール及びアセトンに溶ける。
解説

ボルネオール,モノテルペンアルコールの一つ。竜脳(りゅうのう)、ボルネオ樟脳(しょうのう)ともいわれ、竜脳油、ローズマリー油、ラベンダー油、シトロネラ油など多くの精油中に含まれる。ボルネオールは不斉炭素原子をもっているので3種の光学異性体が存在し、d-体はリュウノウジュ(竜脳樹)より得られ、l-体は中国産竜脳草より得られる。

用途有機合成原料。香粧用として重要。特に酢酸エステルは重要。
応用

ボルネオール,白色板状結晶であり、古くから薫香、墨の香料、香粧品、せっけん香料に使用されている。

説明Borneol is an analgetic, antibacterial, and resuscitation-inducing norborneol derived from fresh branches and leaves of Cinnamomum camphora (L.) Presl. Far more than 2000?years ago, it has been introduced to China . In China, it has been firstly recorded in Ming Yi Bie Lu and then included in Tang Ben Cao. It was recorded in history that borneol was derived from Dryobalanops camphora gaertner and then precipitated from the resin to form the natural crystal compound or distilled from the trunk and cooled down to form the crystal compound, which is certified from Indonesia. In China, the natural borneol mainly relied on imports. In recent years, it was extracted from the Lauraceae plants, including Cinnamomum camphora, Cinnamomum longepaniculatum, and Cinnamomum burmannii, which greatlyincreases the resources of natural borneol for China. Cinnamomum camphora is mainly distributed in Jiangxi and Fujian provinces with 81.78% of borneol. Cinnamomum longepaniculatum is mainly distributed in Hunan and Sichuan provinces with 77.57% of borneol. Cinnamomum burmannii is mainly distributed in Yunnan and Guangxi provinces with 70.81% of borneol. Among them, Cinnamomum camphora contains more borneol than the other two types .
化学的特性white to light yellow crystalline powder or
物理的性質Appearance: colorless to white lumps. Odor: pungent, camphor-like. Density:1.011?g/ cm3 (20?°C). Melting point: 208?°C (406?°F; 481?K). Boiling point: 213?°C (415?°F; 486?K). Solubility: slightly soluble in water (D-form), soluble in chloroform, ethanol, acetone, ether, benzene, toluene, decalin, and tetralin. Flash point: 65? °C (149?°F; 338?K). It’s stable under sealed condition while volatile in the air.
来歴Borneol has been widely used worldwide. It has been systematically studied since 1803 in Dutch literature. This might be because borneol was originated from Indonesia which had been the colony of the Netherlands since the seventeenth century. Stockman reviewed the borneol systematically and conducted the preliminary pharmacological experiments. The current pharmacological studies of borneol focus on crossing blood-brain barrier and its mechanism, as well as promoting the penetration of blood-brain barrier after compatibility with other drugs, which has been started by Qizhong Mo in Shanghai Institute of Materia Medica, Chinese Academy of Sciences since 1982 . Qide Wu et al. synthesized a series of ester derivatives of natural borneol and studied its biological properties. It was found that (+) – 4-methoxybenzoic acid borneol ester had a significant effect on the opening of the blood-brain barrier and was less toxic than borneol . Because of the unique chemical structure of borneol and relatively low molecular weight, borneol is often modified to observe whether the drug has such pharmacological effects of antitumor, increasing the penetration of blood-brain barrier, antibacterial, antioxidant, and others. Up to date, there is no druggability report based on borneol modification.
使用(-)-Borneol has been used to study its antiapoptotic, antioxidative and neuroprotective effect in human neuroblastoma cells (SH-SY5Y).
使用(-)-Borneol is used to prepare its esters by reacting with acids. Its derivatives are used as chiral ligands in asymmetric synthesis. It is also used in flavors and perfumes. Further, it is used in traditional Chinese medicine as moxa. In addition to this, it is used as a component of many essential oils and also used as a natural insect repellent.
適応症The main efficacy of borneol is to induce resuscitation (with aromatic stimulation), clear stagnated fire (fever feeling), remove nebula for improving eyesight, and relieve swelling and pain. The indications of borneol are sore throat, aphthous, red eyes, purulent ear discharge, convulsions, febrile delirium, sudden faint due to qi depression, stroke, and coma. In Chinese traditional medicine, the borneol is often used as an envoy drug and combined with other drugs but is not used as a single medicine with the inexact efficacy
定義ChEBI: (-)-borneol is a borneol. It is an enantiomer of a (+)-borneol.
一般的な説明(-)-Borneol is an enantiomer. It is a bicyclic monoterpene compound used gengrally for analgesia and anaesthesia. It is considered as positive modulators of GABA receptors.
燃焼性と爆発性Flammable
薬理学The main pharmacological effects of borneol include anti-inflammatory, antibacterial, central nervous system, and antifertility effects . Guangchi Jiang found that intraperitoneal injection of borneol at 3.5 mL/kg can significantly inhibit foot swelling caused by egg white in rats. Borneol can inhibit and kill Staphylococcus aureus, B-type Streptococcus, and other five common cells with the minimum inhibitory concentration (MIC) of 1.0–2.0% and the lowest bactericidal concentration (MFC) of 1.5–2.0%. There was significant odinopoeia effect on the late pregnant mice after given 112 mg/kg borneol. Qide Liu et al. found that 10% borneol paraffin oil at the dose of 1 mg/kg by oral gavage can significantly increase the concentration of gentamicin in rat brain tissue, suggesting that borneol can change the blood-brain barrier permeability. The current mechanisms of anti-inflammatory effects include inhibition of inflammatory factors of interleukin-1β, tumor necrosis factor-α, and cell adhesion molecule-1 expression. The mechanisms of central nervous system effects are involved in inhibiting p-glycoprotein, opening the intercellular tight junction, increasing the number of pinocytotic vesicles, and improving the phospholipid molecule arrangement of epithelial cell membrane. In addition, borneol also affects the level of nitric oxide and inhibits the elevation of Ca2+ concentration.
臨床応用As a traditional Chinese medicine, borneol is commonly used as envoy drugs in the compatibility of traditional Chinese medicine. On behalf of combination drugs such as Danshen dripping pills, Niu Huang Jie Du pills, and watermelon cream, its effect is significant because of its special aromatic smell. Borneol with a certain irritation, oral administration may cause the gastrointestinal discomforts, severely causes vomiting and other adverse reactions.
安全性プロファイルMddly toxic by ingestion. A skin irritant. When heated to decomposition it emits acrid smoke and irritating fumes. See also ALCOHOLS.
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