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05680

Sigma-Aldrich

(−)-Alloaromadendrene

≥98.0% (sum of enantiomers, GC)

Synonym(s):

(−)-allo-Aromadendrene

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About This Item

Empirical Formula (Hill Notation):
C15H24
CAS Number:
25246-27-9
Molecular Weight:
204.35
Beilstein:
2357213
MDL number:
MFCD16652612
UNSPSC Code:
12352200
PubChem Substance ID:
329748145
NACRES:
NA.25

Quality Level

100

Assay

≥98.0% (sum of enantiomers, GC)

optical activity

[α]20/D −33±1°, neat

refractive index

n20/D 1.501

bp

265-267 °C (lit.)

density

0.923 g/mL at 20 °C (lit.)

storage temp.

2-8°C

SMILES string

C[C@@H]1CC[C@H]2[C@@H]1[C@H]3[C@@H](CCC2=C)C3(C)C

InChI

1S/C15H24/c1-9-6-8-12-14(15(12,3)4)13-10(2)5-7-11(9)13/h10-14H,1,5-8H2,2-4H3/t10-,11-,12-,13-,14-/m1/s1

InChI key

ITYNGVSTWVVPIC-DHGKCCLASA-N

Application

Alloaromadendrene can be used to study chiral building blocks, complex molecules, chemical syntheses and asymmetric syntheses. Alloaromadendrene has been used to apply headspace solid-phase microextraction (HS-SPME) coupled with GC/FID and GC/MS to the analysis of the volatile fraction of an Ephedra species. Alloaromadendrene has also been used to examine the temporal changes of methyl eugenol metabolites in Bactrocera correcta (guava fruit fly) male rectal glands.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

248.0 °F - closed cup

Flash Point(C)

120.00 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

05680-BULK:
05680-1ML:
05680-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
BCBF9536V
052898/1V
052898/1
052776/1
52898/1

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Jerome Niogret et al.
PloS one, 8(9), e73601-e73601 (2013-09-17)
Chemical analyses were conducted to determine the qualitative and quantitative differences in monoterpenes and sesquiterpenes in plant material from avocado trees, Persea americana Mill. (Lauraceae). The initial study analyzed plant material sampled from the trunk to the leaves through different
Anthony Giampetruzzi et al.
Molecular and cellular neurosciences, 56, 333-341 (2013-07-31)
Fragile X syndrome (FXS) is caused by lack of expression of fragile X mental retardation protein (FMRP), the product of the Fmr1 gene. In many cases FXS is associated with abnormalities in CNS myelination. Although FMRP is expressed in oligodendrocyte
Isao Tokushima et al.
Journal of chemical ecology, 36(12), 1327-1334 (2010-10-23)
The guava fruit fly, Bactrocera correcta, is widely distributed in Thailand and other surrounding Southeast Asian countries, and, like the closely related sympatric species, the oriental fruit fly, B. dorsalis, infests various fruits, including guava, peach, and mango. Males of
Filippo Maggi et al.
Chemistry & biodiversity, 8(1), 95-114 (2011-01-25)
Headspace solid-phase microextraction (HS-SPME) coupled with GC/FID and GC/MS was applied for the first time in the analysis of the volatile fraction of an Ephedra species. Notably, six Italian populations (Marche, Abruzzo, and Sardinia) of Ephedra nebrodensis subsp. nebrodensis, covering

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