W508101
1-Methyl-1,4-cyclohexadiene
≥96%, stabilized
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About This Item
Empirical Formula (Hill Notation):
C7H10
CAS Number:
Molecular Weight:
94.15
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12164502
EC Number:
224-329-6
MDL number:
Organoleptic:
faint
Biological source:
synthetic
Food allergen:
no known allergens
Quality Level
InChI key
QDXQAOGNBCOEQX-UHFFFAOYSA-N
InChI
1S/C7H10/c1-7-5-3-2-4-6-7/h2-3,6H,4-5H2,1H3
SMILES string
CC1=CCC=CC1
biological source
synthetic
assay
≥96%
contains
BHT as stabilizer
refractive index
n20/D 1.471 (lit.)
bp
114-115 °C (lit.)
density
0.838 g/mL at 25 °C (lit.)
application(s)
flavors and fragrances
documentation
see Safety & Documentation for available documents
food allergen
no known allergens
organoleptic
faint
General description
1-Methyl-1,4-cyclohexadiene is reported to be produced by some Nodulosporium species along with other volatile organic compounds (VOCs).
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2
Storage Class
3 - Flammable liquids
flash_point_f
51.8 °F - closed cup
flash_point_c
11 °C - closed cup
Regulatory Information
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An endophytic Nodulisporium sp. producing volatile organic compounds having bioactivity and fuel potential.
Mends MT, et al.
Journal of Petroleum & Environmental Biotechnology, 3(3) (2012)
János P Mészáros et al.
Dalton transactions (Cambridge, England : 2003), 49(23), 7977-7992 (2020-06-06)
Herein the design and synthesis of a new 8-hydroxyquinoline derivative, (S)-5-chloro-7-((proline-1-yl)methyl)8-hydroxyquinoline (HQCl-Pro), with good water solubility and multidrug resistance reversal activity are reported. In this work the proton dissociation processes of HQCl-Pro and its complex formation with [Rh(η5-C5Me5)(H2O)3]2+, [Ru(η6-p-cymene)(H2O)3]2+ and
Hypoxylon sp., an endophyte of Persea indica, producing 1, 8-cineole and other bioactive volatiles with fuel potential.
Tomsheck AR, et al.
Microbial Ecology, 60(4), 903-914 (2010)
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