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Supelco

Nonane

analytical standard

Synonym(s):

n-Nonane

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About This Item

Linear Formula:
CH3(CH2)7CH3
CAS Number:
111-84-2
Molecular Weight:
128.26
Beilstein/REAXYS Number:
1696917
EC Number:
203-913-4
MDL number:
MFCD00009574
UNSPSC Code:
41116107
PubChem Substance ID:
329765577
NACRES:
NA.24

grade

analytical standard

Quality Level

100

vapor density

4.41 (vs air)

vapor pressure

0.18 psi ( 37.7 °C)

assay

≥99.8% (GC)

autoignition temp.

401 °F

shelf life

limited shelf life, expiry date on the label

expl. lim.

2.9 %

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.405 (lit.)
n20/D 1.405

bp

151 °C (lit.)

mp

−53 °C (lit.)

density

0.718 g/mL at 25 °C (lit.)

application(s)

petroleum

format

neat

SMILES string

CCCCCCCCC

InChI

1S/C9H20/c1-3-5-7-9-8-6-4-2/h3-9H2,1-2H3

InChI key

BKIMMITUMNQMOS-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

signalword

Danger

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Central nervous system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

87.8 °F - closed cup

flash_point_c

31.0 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK3932
BCCK0529
BCCC8731
BCBZ2023
BCBV1972

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Jeongmi Choi et al.
Journal of chromatography. A, 1218(41), 7227-7233 (2011-09-13)
In order to analyze amino acids sensitively without derivatization, we have developed carrier-mediated single drop microextraction (SDME). Nonane-1-sulfonic acid was added to an acidic sample donor solution as a carrier to form neutral ion pair complexes with amino acids. The
Johanna Faist et al.
European journal of medicinal chemistry, 45(1), 179-185 (2009-11-03)
N-Alkyl and N-(2-dialkylaminoethyl) derivatives of 5-amino-2-azabicyclo-nonanes were prepared and tested in vitro for their activities against the multidrug-resistant K1 strain of Plasmodium falciparum and Trypanosoma brucei rhodesiense (STIB 900). Most of the new compounds showed lower antitrypanosomal activity than their
Daniel H Ess et al.
Organic letters, 11(23), 5538-5541 (2009-11-11)
Density functional theory was used to locate transition states for hydroboration reactions of allenes with 9-borabicyclo[3.3.1]nonane and 10-R-9-borabicyclo[3.3.2]decane, as well as transition states for [1,3]-boratropic shift and aldehyde addition reactions of the derived allylboranes. The origin of kinetic versus thermodynamic
Arif Baran et al.
The Journal of organic chemistry, 77(3), 1244-1250 (2012-01-11)
1,3,3a,7a-Tetrahydro-2-benzofuran was used as key compound for the synthesis of various bishomoinositol derivatives. The diene was subjected to an epoxidation reaction for further functionalization of the diene unit. The bisepoxide obtained was submitted to a ring-opening reaction with acid in
Franck Slowinski et al.
Organic letters, 12(21), 5004-5007 (2010-10-14)
New azabicyclo[2.2.1]heptane and -[3.3.1]nonane derivatives containing a pyridinyl substituent at the bridgehead position have been synthesized via an efficient ten chemical steps pathway. Both chemical series were then evaluated in vitro for their affinity at α7 nicotinic receptors revealing nanomolar
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