リナロール

リナロール 化学構造式
78-70-6
CAS番号.
78-70-6
化学名:
リナロール
别名:
リナロール;(-)-3,7-ジメチル-1,6-オクタジエン-3-オール;1,5-ジメチル-1-ビニル-4-ヘキセン-1-オール;β-リナロール;d-リナロオール;3,7-ジメチルオクタ-1,6-ジエン-3-オール;β-リナロオール;3,7-ジメチル-1,6-オクタジエン-3-オール;リナロオール;リナリルアルコール;1-エテニル-1,5-ジメチル-4-ヘキセン-1-オール;リナロル;リナロ-ル;3,7ジメチル1,6オクタジエン3オル;リナロ?ル;リナロール, DL-;リナロール, 1000 µg/mL in Ethanol;リナロール, 97%
英語名:
Linalool
英語别名:
1,6-Octadien-3-ol, 3,7-dimethyl-;Linalol;3,7-Dimethyl-1,6-octadien-3-ol;LINALOOL COEUR;3,7-Dimethylocta-1,6-dien-3-ol;Linanool;Phantol;beta-Linalool;Linalool ex orange oil;2,6-dimethyl-2,7-octadien-6-ol (linalool)
CBNumber:
CB5347184
化学式:
C10H18O
分子量:
154.25
MOL File:
78-70-6.mol
MSDS File:
SDS

リナロール 物理性質

融点 :
25°C
沸点 :
194-197 °C/720 mmHg (lit.)
比重(密度) :
0.87 g/mL at 25 °C (lit.)
蒸気圧:
0.17 mm Hg ( 25 °C)
屈折率 :
n20/D 1.462(lit.)
FEMA :
2635 | LINALOOL
闪点 :
174 °F
貯蔵温度 :
2-8°C
溶解性:
エタノール:可溶1ml/4ml、無色透明(60%エタノール)
酸解離定数(Pka):
14.51±0.29(Predicted)
外見 :
液体
比重:
0.860 (20/4℃)
色:
無色透明~淡黄色
PH:
4.5 (1.45g/l, H2O, 25℃)
臭い (Odor):
100.00%で。シトラス フローラル スウィート ボワ ド ローズ ウッディ グリーン ブルーベリー
においのタイプ:
花柄
爆発限界(explosive limit):
0.9-5.2%(V)
水溶解度 :
1.45g/L(25℃)
JECFA Number:
356
Merck :
14,5495
BRN :
1721488
安定性::
安定。強力な酸化剤とは相容れない。可燃性。
InChIKey:
CDOSHBSSFJOMGT-UHFFFAOYSA-N
LogP:
2.9 at 20℃
CAS データベース:
78-70-6(CAS DataBase Reference)
NISTの化学物質情報:
2,6-Dimethylocta-2,7-dien-6-ol(78-70-6)
EPAの化学物質情報:
3,7-Dimethyl-1,6-octadien-3-ol (78-70-6)
安全性情報
  • リスクと安全性に関する声明
  • 危険有害性情報のコード(GHS)
主な危険性  Xi,Xn
Rフレーズ  36/37/38-20/21/22
Sフレーズ  26-36
RIDADR  NA 1993 / PGIII
WGK Germany  1
RTECS 番号 RG5775000
自然発火温度 235 °C
TSCA  Yes
HSコード  29052210
有毒物質データの 78-70-6(Hazardous Substances Data)
毒性 LD50 orally in Rabbit: 2790 mg/kg LD50 dermal Rabbit 5610 mg/kg
消防法 危-4-3-III
化審法 (2)-249, (2)-258
絵表示(GHS) GHS hazard pictograms
注意喚起語 警告
危険有害性情報
コード 危険有害性情報 危険有害性クラス 区分 注意喚起語 シンボル P コード
H315 皮膚刺激 皮膚腐食性/刺激性 2 警告 GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H317 アレルギー性皮膚反応を起こすおそれ 感作性、皮膚 1 警告 GHS hazard pictograms P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
H319 強い眼刺激 眼に対する重篤な損傷性/眼刺激 性 2A 警告 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
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。
P264 取扱い後は皮膚をよく洗うこと。
P264 取扱い後は手や顔をよく洗うこと。
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。
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。

リナロール 価格 もっと(37)

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入
富士フイルム和光純薬株式会社(wako) W01ACSALR-018S-ET-10X リナロール
Linalool, 1000 ug/mL in Ethanol
78-70-6 1mL ¥8900 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) W01ACSALR-018N リナロール
Linalool
78-70-6 100mg ¥8900 2024-03-01 購入
東京化成工業 L0048 リナロール >96.0%(GC)
Linalool >96.0%(GC)
78-70-6 25mL ¥2000 2024-03-01 購入
東京化成工業 L0048 リナロール >96.0%(GC)
Linalool >96.0%(GC)
78-70-6 500mL ¥8500 2024-03-01 購入
関東化学株式会社(KANTO) 12515-3A リナロール
Linalool
78-70-6 100mL ¥8100 2024-03-01 購入

リナロール MSDS


3,7-Dimethyl-1,6-octadien-3-ol

リナロール 化学特性,用途語,生産方法

外観

無色~うすい黄色, 澄明の液体

定義

本品は、次の化学式で表されるテルペンアルコールである。

溶解性

水に難溶。含水エタノールに易溶。エタノールに溶ける。

用途

香料,香料物質の中間体、ビタミンEの合成中間体。

用途

スズラン、ライラックなどの花精油調合に用いられ、香粧品、石けんの香料としてきわめて重要なものである。その他エステル原料にも使用される。

化粧品の成分用途

香料

説明

Linalool has a typical floral odor free from camphoraceous and terpenic notes.1 Synthetic linalool exhibits a cleaner and fresher note than the natural product. It can be prepared synthetically starting from myrcene or from dehydrolinalool.
The optically active forms (d- and ι-) and the optically inactive form occur naturally in more than 2 0 0 oils from herbs, leaves, flowers, and wood; the ι-form is present in the largest amounts (80 - 85%) in the distillates from leaves of Cinnamomum cam phora var. orientalis and Cinnamomum camphora var. occidentalis and in the distillate from Cajenne rosewood; it also has been reported in: champaca, ylang-ylang, neroli, Mexican linaloe, ber gamot, lavandin, and others; a mixture of d- and ι-linalool has been reported in Brazil rosewood (85%); the d-form has been found in palmarosa, mace, sweet orange-flower distillate, petit grain, coriander (60 - 70%), marjoram, Orthodon linalooliferum (80%), and others; the inactive form has been reported in clary sage, jasmine, and Nectandra elaiophora.

化学的特性

Linalool occurs as one of its enantiomers in many essential oils, where it is often the main component. (3R)- (?)-Linalool, for example, occurs at a concentration of 80–85% in Ho oils from Cinnamomum camphora; rosewood oil contains about 80%. (3S)-(+)- Linalool makes up 60–70% of coriander oil (“coriandrol”).
Linalool is used frequently in perfumery for fruity notes and for many floral fragrance compositions (lily of the valley, lavender, and neroli). Because of its relatively high volatility, it imparts naturalness to top notes. Since linalool is stable in alkali, it can be used in soaps and detergents. Linalyl esters can be prepared from linalool.Most of the manufactured linalool is used in the production of vitamin E.

物理的性質

Properties. Racemic linalool is, similarly to the individual enantiomers, a colorless liquid with a floral, fresh odor, reminiscent of lily of the valley. However, the enantiomers differ slightly in odor. Together with its esters, linalool is one of the most frequently used fragrance substances and is produced in large quantities. In the presence of acids, linalool isomerizes readily to geraniol, nerol, and α-terpineol. It is oxidized to citral, for example, by chromic acid. Oxidation with peracetic acid yields linalool oxides, which occur in small amounts in essential oils and are also used in perfumery. Hydrogenation of linalool gives tetrahydrolinalool, a stable fragrance material. Its odor is not as strong as, but is fresher than, that of linalool. Linalool can be converted into linalyl acetate by reaction with ketene or with an excess of boiling acetic anhydride.

天然物の起源

The optically active forms (d- and l-) and the optically inactive form occur naturally in more than 200 oils from herbs, leaves, flowers and wood; the l-form is present in the largest amounts (80 to 85%) in the distillates from leaves of Cinnamomum camphora var. orientalis and Cinnamomum camphora var. occidentalis and in the distillate from Cajenne rosewood; it also has been reported in champaca, ylang-ylang, neroli, Mexican linaloe, bergamot and lavandin; a mixture of d- and l-linalool has been reported in Brazil rosewood (85%); the d-form has been found in palmarosa, mace, sweet orange-flower distillate, petitgrain, coriander (60 to 70%), marjoram and Orthodon linalooliferum (80%); the inactive form has been reported in clary sage, jasmine and Nectandra elaiophora. Also reported found in over 280 products including apple, citrus peel oils and juices, berries, grapes, guava, celery, peas, potato, tomato, cinnamon, cloves, cassia, cumin, ginger, mentha oils, mustard, nutmeg, pepper, thymus, cheeses, grape wines, butter, milk, rum, cider, tea, passion fruit, olive, mango, beans, coriander, cardamom and rice.

使用

linalool is a fragrant component of both lavender and coriander. It can be incorporated into cosmetics for perfuming, deodorant, or odor-masking activity.

定義

ChEBI: A monoterpenoid that is octa-1,6-diene substituted by methyl groups at positions 3 and 7 and a hydroxy group at position 3. It has been isolated from plants like Ocimum canum.

一般的な説明

Linalool is a monoterepene compound. It is the major component of many essential oils. Anti-inflammatory properties of (?) linalool, a naturally occurring enantiomer, has been studied. It is also the major constituent of the basil and thyme essential oil and its anti-microbial effect was determined using the agar well diffusion assay. Linalool is reported to have dose-dependent marked sedative effects at the central nervous system (CNS), including hypnotic, anticonvulsant and hypothermic properties. Linalool is reported to have a lemon like odor.

接触アレルゲン

Linalool is a terpene chief constituent of linaloe oil,also found in oils of Ceylon cinnamon, sassafras,orange flower, bergamot, Artemisia balchanorum, ylang-ylang. This frequently used scented substance is a sensitizer by the way of primary or secondary oxida-tion products. As a fragrance allergen, linalool has to be mentioned by name in cosmetics within the EU

抗がん研究

Studies of antitumor activities and toxicity were done on solid S-180 tumor-bearingSwiss albino mice. It results in an induction of oxidative stress with an antitumoractivities result. In comparison with cyclophosphamide, antioxidant effects wereobserved in the liver and modulation of proliferation of spleen cells in tumor-bearingmice challenged with lipopolysaccharides, while both were seriously affected bycyclophosphamide (Costa et al. 2015).

リナロール 上流と下流の製品情報

原材料

準備製品


リナロール 生産企業

Global( 667)Suppliers
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リナロール  スペクトルデータ(1HNMR、13CNMR、IR1、MS、Raman)


78-70-6(リナロール)キーワード:


  • 78-70-6
  • femanumber2635
  • Linalool ex ho oil
  • 2,6-Dimethyl-2,7-octadiene-6-ol
  • 3,7-dimethyl-1,6-octadien-3-ol (linalool)
  • 3,7-dimethyl-1,6-octandien-3-ol (linalool)
  • Linalool 97%
  • Linalool 2,6-Dimethylocta-2,7-dien-6-ol
  • Linolool
  • LINOLOOL (D)
  • LINALOOL PURE
  • Linalool, 97% 500ML
  • (±)-3,7-dimethyl-octa-1,6-dien-3-ol
  • (±)-3,7-Dimethylocta-1,6-dien-3-ol
  • 3,7-DIMETHYLOCT-1,6-DIEN-3-OL
  • Linalool(1,1,2-D3)
  • LINALOOL 96+% FCC
  • Linalool,97%
  • linalool,3,7-dimethylocta-1,6-dien-3-ol,2,6-dimethylocta-2,7-dien-6-ol(R,S,andracemate)
  • LINALLOL
  • LINALOOL NATUERLICH
  • (±)-3,7-Dimethyl-1,6-octadien-3-ol, (±)-3,7-Dimethyl-3-hydroxy-1,6-octadiene, Linalool
  • (±)-3,7-Dimethyl-1,6-octadien-3-ol, (±)-3,7-Dimethyl-3-hydroxy-1,6-octadiene
  • Linalool
  • LINALOOL SYNTHETIC TECH. GRADE
  • LINALOOL, NATURAL EX-BASIL
  • 3,7-Dimethylocta-1,6-diene-3-ol
  • Octadien-3-ol, 3,7-dimethyl-
  • Linalool,(±)-3,7-Dimethyl-1,6-octadien-3-ol, (±)-3,7-Dimethyl-3-hydroxy-1,6-octadiene
  • 3.7-Dimethyl-1.6-octadien-3-ol 1g [78-70-6]
  • Linalool,(±)-3,7-Dimethyl-1,6-octadien-3-ol, (±)-3,7-Dimethyl-3-hydroxy-1,6-octadiene, Linalool
  • リナロール
  • (-)-3,7-ジメチル-1,6-オクタジエン-3-オール
  • 1,5-ジメチル-1-ビニル-4-ヘキセン-1-オール
  • β-リナロール
  • d-リナロオール
  • 3,7-ジメチルオクタ-1,6-ジエン-3-オール
  • β-リナロオール
  • 3,7-ジメチル-1,6-オクタジエン-3-オール
  • リナロオール
  • リナリルアルコール
  • 1-エテニル-1,5-ジメチル-4-ヘキセン-1-オール
  • リナロル
  • リナロ-ル
  • 3,7ジメチル1,6オクタジエン3オル
  • リナロ?ル
  • リナロール, DL-
  • リナロール, 1000 µg/mL in Ethanol
  • リナロール, 97%
  • 非環式モノテルペン
  • 生化学
  • テルペン
  • 誘引剤
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