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W278904

Sigma-Aldrich

Nonyl alcohol

≥98%, FCC

Synonym(s):

1-Nonanol, 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
FEMA Number:
2789
Beilstein:
969213
EC Number:
205-583-7
Council of Europe no.:
55
MDL number:
MFCD00002990
UNSPSC Code:
12164502
PubChem Substance ID:
24901330
Flavis number:
2.007
NACRES:
NA.21

biological source

synthetic

Quality Level

400

grade

Halal
Kosher

Agency

meets purity specifications of JECFA

reg. compliance

FCC
FDA 21 CFR 172.515

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.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

Organoleptic

citrus; floral

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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Application


  • Synthesis, X-ray crystal structures, thermal and electrochemical properties of thiosemicarbazidatodioxouranium(VI) complexes.: The article details the synthesis and characterization of uranium complexes involving Nonyl alcohol. The study provides insights into the structural and electrochemical properties of these complexes, contributing to the field of coordination chemistry. (Sahin et al., 2010).

Disclaimer

For R&D or non-EU Food use. Not for retail sale.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H319,H412

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)

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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
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
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
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
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