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| 4-(1-メチルエテニル)-1-シクロヘキセン-1-メタノール 製品概要 |
化学名: | 4-(1-メチルエテニル)-1-シクロヘキセン-1-メタノール | 英語化学名: | DIHYDRO CUMINYL ALCOHOL | 别名: | DIHYDRO CUMINYL ALCOHOL;Perilla alcohol
Dihydrocuminyl alcohol;(4-Isopropenyl-1-cyclohexen-1-yl)methanol;4-(1-methylethenyl)-1-cyclohexene-1-methano;1-HYDROXYMETHYL-4-(1-METHYLVINYL)-CYCLOHEXENE;PARA-MENTHA-1,8-DIEN-7-OL;(4-prop-1-en-2-yl-1-cyclohexenyl)methanol;PERILLYL ALCOHOL, (-)-(RG) | CAS番号: | 536-59-4 | 分子式: | C10H16O | 分子量: | 152.23 | EINECS: | 208-639-9 | カテゴリ情報: | Benzhydrols, Benzyl & Special Alcohols;Furans ,Coumarins | Mol File: | 536-59-4.mol | |
| 4-(1-メチルエテニル)-1-シクロヘキセン-1-メタノール 物理性質 |
| 4-(1-メチルエテニル)-1-シクロヘキセン-1-メタノール Usage And Synthesis |
定義 | 本品は、次の化学式で表されるアルコールである。 | 化粧品の成分用途 | 皮膚保護剤、殺菌剤、酸化防止剤、香料 | 説明 | p-Mentha-1,8-dien-7-ol has a characteristic odor similar to linalool
and terpineol. The L-form is obtained starting from (3-pinene or by
reducing perillic aldehyde with zinc dust and acetic acid, followed
by saponification of the acetate. | 化学的特性 | p-Mentha-1,8-dien-7-ol has a characteristic odor similar to linalool and terpineol. | 化学的特性 | clear colorless to light yellow liquid | 天然物の起源 | The d- and l-forms occur naturally in gingergrass essential oil; the l-form is found in lavandin and bergamot,
while the d-form is found in caraway; also reported found in the essential oils of Juniperus sabina L. and East Indian geranium. Also
reported found in citrus peel oils, berries, peppermint oil, Scotch peppermint oil, hop oil, cardamom, laurel, lemon balm, lamb’s let tuce, mastic gum oil and bullock’s head (Annona reticulata). | 使用 | (4-(Prop-1-en-2-yl)cyclohex-1-en-1-yl)methanol is used in preparation of perilla alcohol leaf alcohol carbonate as perfume. | 使用 | antineoplastic, apoptosis inducer; skin irritant, LD50(rat) 2100 mg/kg po | 定義 | ChEBI: A limonene monoterpenoid consists of a cyclohexene ring substituted by a hydroxymethyl and a prop-1-en-2-yl group at positions 1 and 4 respectively. It is a constituent of a variety of essential oils including lavender. | 製造方法 | The l-form is obtained starting from β-pinene or by reducing perillic aldehyde with zinc dust and acetic acid, followed
by saponification of the acetate. | Aroma threshold values | Detection: 7 ppm | 安全性プロファイル | Moderately toxic by ingestion. A severe skin irritant. Combustible liquid. When heated to decomposition it emits acrid smoke and irritating fumes. |
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