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等級
analytical standard
品質等級
化驗
≥98.5% (sum of enantiomers, GC)
光學活性
[α]20/D +61±2°, neat
儲存期限
limited shelf life, expiry date on the label
技術
HPLC: suitable
gas chromatography (GC): suitable
折射率
n20/D 1.499
bp
228-230 °C (lit.)
密度
0.960 g/mL at 20 °C (lit.)
應用
agriculture
environmental
food and beverages
格式
neat
SMILES 字串
CC(=C)[C@H]1CC=C(C)C(=O)C1
InChI
1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9H,1,5-6H2,2-3H3/t9-/m0/s1
InChI 密鑰
ULDHMXUKGWMISQ-VIFPVBQESA-N
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相关类别
一般說明
（+）-香芹酮（S-香芹酮）是一种单萜，具有影响植物生长发育和微生物活性调节的能力，它还可以通过抑制苯丙氨酸氨裂合酶（PAL）的诱导来防止马铃薯发芽。
應用
有关合适的仪器技术的更多信息，请参阅产品′的检验报告。想要获得更多支持，请联系技术服务部。
其他說明
This compound is commonly found in plants of the genus: carum mentha zingiber
訊號詞
Warning
危險聲明
危險分類
Skin Sens. 1A
儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 1
閃點（°F）
204.1 °F - closed cup
閃點（°C）
95.6 °C - closed cup
個人防護裝備
Eyeshields, Gloves
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Lippia alba (Mill.) N.E. Brown (Verbenaceae) is widely used in different regions of Central and South America as a tranquilizer. The plant's anxiolytic properties, however, merit investigation. The present study evaluated the effects of repeated daily (14 days) intraperitoneal (ip)
Marta Goretti et al.
Bioresource technology, 121, 290-297 (2012-08-04)
Response surface methodology was applied in optimizing the asymmetric bioreduction of (4S)-(+)-carvone to dihydrocarvone (with low incidence of unsought side reactions) by using whole-cells of Cryptococcus gastricus. A factorial design (2(5)) including five independent variables was performed: X(1)=incubation time; X(2)=pH;
Raul Conde et al.
Phytomedicine : international journal of phytotherapy and phytopharmacology, 18(14), 1197-1201 (2011-08-02)
There is no universally accepted and effective prophylaxis of migraine headache episodes. Thus we aimed to investigate the effects of Lippia alba (Mill.) N. E. Brown, an herb with many effects on central nervous system, on pain frequency and intensity
Elissavet E Anagnostaki et al.
Organic letters, 15(1), 152-155 (2012-12-22)
The synthesis of hydroxyelemane 5 from (R)-carvone and its utilization as a common synthetic scaffold to produce structurally diverse germacrane and guaiane sesquiterpenes are described. A highly enantio- and stereoselective biomimetic tandem oxy-Cope/ene rearrangement was used as the key reaction
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