131210
1-Nonanol
98%
Synonym(s):
Alcohol C9, Nonyl alcohol
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£40.30
500 ML
£64.60
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100 ML
£40.30
500 ML
£64.60
About This Item
Linear Formula:
CH3(CH2)8OH
CAS Number:
Molecular Weight:
144.25
Beilstein:
969213
EC Number:
MDL number:
UNSPSC Code:
12352100
eCl@ss:
39020223
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
vapor density
5 (vs air)
vapor pressure
13 mmHg ( 104 °C)
Assay
98%
form
liquid
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.)
functional group
hydroxyl
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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General description
1-Nonanol inhibited the bacterial luciferase (BL) reaction in a dose-dependent manner[1].
Application
1-Nonanol can be used:
- As a reference material in the determination of airborne fungal spore levels using GC-MS method.[2]
- To prepare polysulfone capsules as ideal adsorbents used in the removal of phenol from an aqueous solution.[3]
- As a solvent in the study of swelling properties of hummers graphene oxide membranes.[4]
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 3 - Eye Irrit. 2
Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Flash Point(F)
208.4 °F - closed cup
Flash Point(C)
98 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Swelling of graphene oxide membranes in alcohols: effects of molecule size and air ageing
Iakunkov A, et al.
Journal of Material Chemistry A, 7(18), 11331-11337 (2019)
A L Sunesson et al.
The Annals of occupational hygiene, 40(4), 397-410 (1996-08-01)
Two fungal species commonly found in indoor environments, Penicillium commune and Paecilomyces variotü, were cultivated on pine wood and on a combination of gypsum board and mineral wool. Air from the cultures was adsorbed on Tenax TA and analysed using
M Hori et al.
Journal of pharmaceutical sciences, 81(4), 330-333 (1992-04-01)
The fluxes of representative hydrophilic (propranolol hydrochloride) and lipophilic (diazepam or indomethacin) drugs, administered as ethanolic solutions containing putative penetration enhancers (n-nonane, 1-nonanol, and 1-decanol), were measured across hairless mouse skin in vitro. Propranolol transport was augmented significantly by the
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
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
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