N1754
1-Nonanol
~98%
Synonym(s):
Alcohol C9, Nonyl alcohol
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About This Item
Linear Formula:
CH3(CH2)8OH
CAS Number:
Molecular Weight:
144.25
EC Number:
205-583-7
UNSPSC Code:
12352200
MDL number:
Beilstein/REAXYS Number:
969213
vapor density
5 (vs air)
vapor pressure
13 mmHg ( 104 °C)
assay
~98%
refractive index
n20/D 1.433 (lit.)
bp
215 °C (lit.)
mp
−8-−6 °C (lit.)
density
0.827 g/mL at 25 °C (lit.)
SMILES string
CCCCCCCCCO
InChI
1S/C9H20O/c1-2-3-4-5-6-7-8-9-10/h10H,2-9H2,1H3
InChI key
ZWRUINPWMLAQRD-UHFFFAOYSA-N
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signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 3 - Eye Irrit. 2
Storage Class
10 - Combustible liquids
wgk
WGK 2
flash_point_f
208.4 °F - closed cup
flash_point_c
98 °C - closed cup
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G Mougabure Cueto et al.
Journal of medical entomology, 39(3), 457-460 (2002-06-14)
The effectiveness of 1-octanol, 1-nonanol, 1-decanol, 1-undecanol, and 1-dodecanol was evaluated by immersion method against susceptible and permethrin-resistant head lice, Pediculus humanus capitis De Geer, from Buenos Aires, Argentina. All the tested alcohols showed knockdown effect at 10 min and
Mathias Ditzen et al.
Chemical senses, 28(9), 781-789 (2003-12-05)
The brain's link between perception and action involves several steps, which include stimulus transduction, neuronal coding of the stimulus, comparison to a memory template and choice of an appropriate behavioral response. All of these need time, and many studies report
Guanghui Zhao et al.
Journal of hazardous materials, 175(1-3), 715-725 (2009-11-21)
This study investigated the potential of capsules containing 1-nonanol for the adsorption of phenol at high initial concentrations. The polysulfone capsules containing 1-nonanol (PSF@1-nonanol capsules) were successfully prepared with a phase inversion method, and the results showed that 1-nonanol was
Emmanuel Perisse et al.
BMC biology, 7, 30-30 (2009-06-18)
Synaptic plasticity associated with an important wave of gene transcription and protein synthesis underlies long-term memory processes. Calcium (Ca2+) plays an important role in a variety of neuronal functions and indirect evidence suggests that it may be involved in synaptic
D M Greene-McDowelle et al.
Toxicon : official journal of the International Society on Toxinology, 37(6), 883-893 (1999-05-26)
The fungi Aspergillus flavus and Aspergillus parasiticus produce the hepatocarcinogenic, secondary metabolites, aflatoxins, in cottonseed, corn, peanuts and treenuts. Results have shown that aflatoxigenic strains of A. flavus and A. parasiticus grown in the presence of specific cotton-leaf volatiles exhibit
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