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53675

Sigma-Aldrich

α-Humulene

≥96.0% (GC)

Sinonimo/i:

alpha-Humulene, α-Caryophyllene, trans,trans,trans-2,6,6,9-Tetramethyl-1,4,8-cycloundecatriene

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About This Item

Formula empirica (notazione di Hill):
C15H24
Numero CAS:
6753-98-6
Peso molecolare:
204.35
Beilstein:
3240075
Numero CE:
229-816-7
Numero MDL:
MFCD00042689
Codice UNSPSC:
12352100
ID PubChem:
57651429
NACRES:
NA.22

Saggio

≥96.0% (GC)

Indice di rifrazione

n20/D 1.503 (lit.)

P. ebollizione

166-168 °C (lit.)

Densità

0.889 g/mL at 20 °C (lit.)

Temperatura di conservazione

2-8°C

Stringa SMILE

C\C1=C/CC(C)(C)\C=C\C\C(C)=C\CC1

InChI

1S/C15H24/c1-13-7-5-8-14(2)10-12-15(3,4)11-6-9-13/h6-7,10-11H,5,8-9,12H2,1-4H3/b11-6+,13-7+,14-10+
FAMPSKZZVDUYOS-HRGUGZIWSA-N

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Descrizione generale

α-Humulene is a class of sesquiterpenes found in Cordia verbenacea essential oil.[1]

Applicazioni

α-Humulene can be used in the formation of secondary organic aerosol by oxidation.[2]

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H335

Classi di pericolo

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

194.0 °F - closed cup

Punto d’infiammabilità (°C)

90 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificati d'analisi (COA)

Lot/Batch Number
BCBV7891
BCBP7751V
BCBN2536V
BCBF5297V
BCBC2770V

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Rafael C Dutra et al.
The Journal of pharmacy and pharmacology, 61(2), 243-250 (2009-01-31)
The objective of this work was to investigate the antiulcerogenic and anti-inflammatory activities of the essential oil from Pterodon emarginatus seeds. The following tests were used: ulcers induced by ethanol, indometacin and HCl/ethanol, and pleurisy induced by carrageenan in Swiss
Ping-Chuan Jiang et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 32(8), 1224-1227 (2009-12-08)
To study the volatile oil of Murraya exotica. The volatile oil of Murraya exotica was extracted by steam-stilling and was identified by GC-MS-DS. More than 90 compounds were separated, and 59 compounds were identified, accounting for 93.9% of the total
Ling Chai et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 33(3), 382-385 (2010-08-05)
To analyze the compositions of the essential oil from the leaves of Callicarpa integerrima. GC-MS method was used. 42 chemical constituents, accounting for 97.62% of total content were identified. The main components were beta-caryophyllene (33.74%), Elixene (12.86%), tau-Cadinene (9.57%) and
M Beck et al.
Physical chemistry chemical physics : PCCP, 13(23), 10970-11001 (2011-04-05)
α-Humulene contains three double bonds (DB), and after ozonolysis of the first DB the first-generation products are still reactive towards O(3) and produce second- and third-generation products. The primary aim of this study consisted of identifying the products of the
Akinola O Ogunbinu et al.
Natural product communications, 4(3), 421-424 (2009-05-06)
The chemical composition of the essential oils from the leaves and stem bark of Eclipta prostrata (L.) L. and the aerial parts of Vernonia amygdalina Delile (Asteraceae) have been analyzed by capillary gas chromatography (GC) and gas chromatography/mass spectrometry (GC/MS).
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