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Merck
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131210

Sigma-Aldrich

1-Nonanol

98%

Sinônimo(s):

Alcohol C9, Nonyl alcohol

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About This Item

Fórmula linear:
CH3(CH2)8OH
Número CAS:
Peso molecular:
144.25
Beilstein:
969213
Número CE:
Número MDL:
Código UNSPSC:
12352100
eCl@ss:
39020223
ID de substância PubChem:
NACRES:
NA.22

densidade de vapor

5 (vs air)

pressão de vapor

13 mmHg ( 104 °C)

Ensaio

98%

forma

liquid

índice de refração

n20/D 1.433 (lit.)

pb

215 °C (lit.)

pf

−8-−6 °C (lit.)

densidade

0.827 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

CCCCCCCCCO

InChI

1S/C9H20O/c1-2-3-4-5-6-7-8-9-10/h10H,2-9H2,1H3

chave InChI

ZWRUINPWMLAQRD-UHFFFAOYSA-N

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Descrição geral

1-Nonanol inhibited the bacterial luciferase (BL) reaction in a dose-dependent manner.

Aplicação

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.

Pictogramas

Exclamation mark

Palavra indicadora

Warning

Frases de perigo

Declarações de precaução

Classificações de perigo

Aquatic Chronic 3 - Eye Irrit. 2

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

208.4 °F - closed cup

Ponto de fulgor (°C)

98 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


Certificados de análise (COA)

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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
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
Shinya Yamasaki et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 27(4), 357-357 (2011-04-12)
An electrochemical system has been developed in order to assay the effect of hydrophobic molecules on the bioluminescence of bacterial luciferase (BL). The inhibition of BL luminescence by the long-chain n-alkyl alcohol has been examined using this system. The 1-heptanol

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