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Sigma-Aldrich

1-Nonanol

98%

Synonym(s):

Alcohol C9, Nonyl alcohol

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About This Item

Linear Formula:
CH3(CH2)8OH
CAS Number:
143-08-8
Molecular Weight:
144.25
Beilstein:
969213
EC Number:
205-583-7
MDL number:
MFCD00002990
UNSPSC Code:
12352100
eCl@ss:
39020223
PubChem Substance ID:
24848002
NACRES:
NA.22

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.)

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.

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.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H319,H412

Precautionary Statements

P273 - P305 + P351 + P338

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
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
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