235172
(+)-长叶烯
≥98%
别名:
(1R,2S,7S,9S)-3,3,7-三甲基-8-亚甲基三环[5.4.0.02.9]十一烷, Junipene, Kuromatsuene, [1S-(1α,3aβ,4α,8aβ)]-十氢-4,8,8-三甲基-9-亚甲基-1,4-甲桥薁
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关于此项目
经验公式（希尔记法）:
C15H24
化学文摘社编号:
分子量:
204.35
EC Number:
207-491-2
UNSPSC Code:
12352103
PubChem Substance ID:
Beilstein/REAXYS Number:
2044263
MDL number:
InChI key
PDSNLYSELAIEBU-WOFVOEOOSA-N
InChI
1S/C15H24/c1-10-11-6-7-12-13(11)14(2,3)8-5-9-15(10,12)4/h11-13H,1,5-9H2,2-4H3/t11?,12?,13?,15-/m0/s1
SMILES string
CC1(C)CCC[C@]2(C)C3CCC(C13)C2=C
assay
≥98%
optical activity
[α]22/D +46°, neat
refractive index
n20/D 1.504 (lit.)
bp
254 °C/706 mmHg (lit.)
density
0.928 g/mL at 25 °C (lit.)
signalword
Danger
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Skin Sens. 1
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
213.8 °F - closed cup
flash_point_c
101.00 °C - closed cup
ppe
Eyeshields, Gloves
法规信息
新产品
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Lethal and sublethal effects of azulene and longifolene to Microtox(R), Ceriodaphnia dubia, Daphnia magna, and Pimephales promelas.
L I Sweet et al.
Bulletin of environmental contamination and toxicology, 58(2), 268-274 (1997-02-01)
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Se pu = Chinese journal of chromatography, 20(6), 577-581 (2003-04-10)
A method for the separation and determination of terpineol oil by temperature programming capillary gas chromatography has been established. An OV-1 fused silica capillary column (30 m x 0.32 mm i.d. x 0.25 microns) was used with a temperature increase
P B Pedersen et al.
Natural toxins, 7(6), 305-309 (2000-12-21)
This paper reviews the toxicology of culmorins, a family of compounds found in grains contaminated by Fusarium graminearum and related fungi. We include the results of an Ames test and studies based on Quantitative Structure-Activity Relationships. Culmorin has low toxicity
Huashou Li et al.
Ying yong sheng tai xue bao = The journal of applied ecology, 16(4), 763-767 (2005-07-14)
This paper studied the allelopathic effects of Cymbopogon citratus volatile on the seed germination and seedling growth of corn and barnyard grass (Echinochloa crusgalli) in field and in obturator, and analyzed the chemical components of the volatile with SPME and
Gopal Subramaniam et al.
Magnetic resonance in chemistry : MRC, 44(12), 1118-1121 (2006-09-27)
We describe the conformation and stereospecific 1H and 13C chemical shift assignments of longifolene 1 and its penultimate precursor 2 through the combined use of ab initio calculations and experimental NMR techniques. The predicted stable conformation for both compounds was
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