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53675

α-Humulene

≥96.0% (GC)

Sinonimo/i:

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

Autenticati per visualizzare i prezzi organizzativi e contrattuali.

Informazioni su questo articolo

Formula empirica (notazione di Hill):
C15H24
Numero CAS:
6753-98-6
Peso molecolare:
204.35
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
57651429
EC Number:
229-816-7
Beilstein/REAXYS Number:
3240075
MDL number:
MFCD00042689
Assay:
≥96.0% (GC)

assay

≥96.0% (GC)

refractive index

n20/D 1.503 (lit.)

bp

166-168 °C (lit.)

density

0.889 g/mL at 20 °C (lit.)

storage temp.

2-8°C

SMILES string

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+

InChI key

FAMPSKZZVDUYOS-HRGUGZIWSA-N

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General description

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

Application

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

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Classe di stoccaggio

10 - Combustible liquids

wgk

WGK 3

flash_point_f

194.0 °F - closed cup

flash_point_c

90 °C - closed cup

ppe

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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Shin-Pin Chen et al.
Chemical & pharmaceutical bulletin, 57(2), 162-166 (2009-02-03)
A novel skeletal norhumulene (1) and six xeniaphyllane-derived compounds, including norditerpenoids (2, 3) and diterpenoids (4-7), were isolated from the EtOAc extract of the Formosan soft coral Sinularia gibberosa. Their structures were elucidated by spectroscopic analysis. In vitro cytotoxic evaluation
Secondary organic aerosol formation from the oxidation of a series of sesquiterpenes: α-cedrene, β-caryophyllene, α-humulene and α-farnesene with O3, OH and NO3 radicals
Jaoui M, et al.
Environmental Chemistry, 10(3), 178-193 (2013)
Rosa Tundis et al.
Natural product research, 23(18), 1707-1718 (2009-11-19)
This study is aimed to evaluate the in vitro cytotoxicity of Senecio stabianus Lacaita (Asteraceae) against renal adenocarcinoma ACHN, hormone-dependent prostate carcinoma LNCaP, amelanotic melanoma C32 and human breast adenocarcinoma MCF-7 cell lines. The n-hexane extract showed an interesting activity
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
Ulrich Neuenschwander et al.
The Journal of organic chemistry, 77(6), 2865-2869 (2012-02-16)
Humulene is a sesquiterpene with an important biochemical lead structure, consisting of an 11-membered ring, containing three nonconjugated C═C double bonds, two of them being triply substituted and one being doubly substituted. As observed by many groups, one of the
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Protocolli

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GC Analysis of Sweet Orange Essential Oil on SLB®-5ms (10 m x 0.10 mm I.D., 0.10 μm), Fast GC Analysis

Numero articolo commerciale globale

SKUGTIN
53675-1ML04061832565453
53675-5ML04061832565460

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