7785-26-4
中文名稱
左旋-alpha-蒎烯
英文名稱
(1S)-(-)-alpha-Pinene
CAS
7785-26-4
EINECS 編號
232-077-3
分子式
C10H16
MDL 編號
MFCD00064145
分子量
136.23
MOL 文件
7785-26-4.mol
更新日期
2025/04/14 09:47:55
7785-26-4 結(jié)構(gòu)式
基本信息
中文別名
左旋-alpha-蒎烯(1S)-(-)-α蒎烯
(1S)-2,6,6-三甲基-二環(huán)[3.1.1]庚-2-烯
蒎烯
(1S)-(-)-α-蒎烯
(-)-Α-蒎烯,98%,含有數(shù)量不等的異構(gòu)體
英文別名
(1s)-2,6,6-trimethylbicyclo[3.1.1]hept-2-ene(1S)-(-)-a-pinene
(1S)-(-)-pin-2-ene
(1S)-(-)-α-pinene
(1S)-2,6,6-trimethylbicyclo[3.1.1]-2-heptene
(1S,5S)-(-)-α-pinene
(S)-(-)-α-pinene
1S-(-)-a-pinene
2,6,6-trimethyl-,(1S)-Bicyclo[3.1.1]hept-2-ene
2-pinene,(1S,5S)-(-)-
6,6-trimethyl-(1s)-bicyclo[3.1.1]hept-2-en
Bicyclo[3.1.1]hept-2-ene, 2,6,6-trimethyl-, (1S)-
bicyclo[3.1.1]hept-2-ene,2,6,6-trimethyl-,(1S)-
l-α-pinene
α-pinene,(1S)-(-)-
(1S)-(-)-ALPHA-PINENE 99+% (87+% EE/GL&
Pinene,96%
(1S)-(-)-ALPHA-PINENE, 99+% (87+% E.E.)
(1S)-(-)-ALPHA-PINENE, 98% (81+% E.E.)
(1S)-(-)-ALPHA-PINENE 98+% FCC
所屬類別
生物化工：提取物物理化學(xué)性質(zhì)
外觀性質(zhì)無色透明液體，有松節(jié)油的氣味,不溶于水，溶于無水乙醇、乙醚、氯仿等多數(shù)有機(jī)溶劑。閃點:33℃熔點:-64℃沸點:156℃折光率:1.466密度:0.858[α]20D -45.5 ° (C=neat)
熔點-64 °C(lit.)
比旋光度-41.5 º (c=neat)
沸點156-158 °C(lit.)
密度0.874 g/mL at 25 °C
蒸氣密度4.7 (vs air)
蒸氣壓~3 mm Hg ( 20 °C)
FEMA2902
折射率n20/D 1.466
閃點90 °F
儲存條件2-8°C
溶解度氯仿（微溶）、甲醇（微溶）
形態(tài)液體
顏色透明無色
氣味 (Odor)at 10.00 % in dipropylene glycol. sharp warm resinous fresh pine
爆炸極限值(explosive limit)0.8%(V)
生物來源Pinus spp.
香型herbal
旋光性 (optical activity)[α]22/D 42°, neat
水溶解性INSOLUBLE
JECFA Number1329
Merck14,7445
檢測方法GC
BRN1903790
InChIKeyGRWFGVWFFZKLTI-UHFFFAOYSA-N
LogP4.48 at 37℃
CAS 數(shù)據(jù)庫7785-26-4(CAS DataBase Reference)
NIST化學(xué)物質(zhì)信息(1s)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene(7785-26-4)
EPA化學(xué)物質(zhì)信息2-Pinene, (1S,5S)-(-)- (7785-26-4)
安全數(shù)據(jù)
知名試劑公司產(chǎn)品信息
Acros Organics
(1S)-(-)-alpha-蒎烯(1S)-(-)-alpha-Pinene, 98%(7785-26-4)
Sigma Aldrich
7785-26-4(sigmaaldrich)常見問題列表
生物活性
(-)-α-Pinene 是一種單萜類化合物，通過在 BZD 結(jié)合位點作為部分調(diào)節(jié)劑與 GABAA-苯二氮卓 (BZD) 受體直接結(jié)合，顯示出增強(qiáng)睡眠的特性。靶點
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Human Endogenous Metabolite
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體外研究
(-)-α-pinene enhances the quantity of non-rapid eye movement sleep (NREMS) without affecting the intensity of NREMS by prolonging GABAergic synaptic transmission, acting as a partial modulator of GABAA-BZD receptors and directly binding to the BZD binding site of GABAA receptor.