131210
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
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39020223
UNSPSC Code:
12352100
EC Number:
205-583-7
MDL number:
Beilstein/REAXYS Number:
969213
Assay:
98%
Form:
liquid
vapor density
5 (vs air)
Quality Level
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
General description
1-Nonanol inhibited the bacterial luciferase (BL) reaction in a dose-dependent manner.
Application
1-Nonanol can be used:
- As a reference material in the determination of airborne fungal spore levels using GC-MS method.
- To prepare polysulfone capsules as ideal adsorbents used in the removal of phenol from an aqueous solution.
- As a solvent in the study of swelling properties of hummers graphene oxide membranes.
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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
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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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
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