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Merck
CN

N4004

Nonane

≥99% (GC)

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
EC Number:
203-913-4
UNSPSC Code:
12352200
MDL number:
MFCD00009574
Beilstein/REAXYS Number:
1696917

Key Documents

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InChI

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

InChI key

BKIMMITUMNQMOS-UHFFFAOYSA-N

SMILES string

CCCCCCCCC

vapor density

4.41 (vs air)

vapor pressure

0.18 psi ( 37.7 °C)

assay

≥99% (GC)

autoignition temp.

401 °F

expl. lim.

2.9 %

bp

151 °C (lit.)

mp

−53 °C (lit.)

density

0.718 g/mL at 25 °C (lit.)

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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

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

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
091K3687
062H3702
055H3715
053H3429
052K3694

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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
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
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
Lip Kim Lee et al.
Applied and environmental microbiology, 76(3), 794-802 (2009-12-17)
Polybrominated diphenyl ethers (PBDEs) have attracted attention recently due to their proven adverse effects on animals and their increasing concentrations in various environmental media and biota. To gain insight into the fate of PBDEs, microcosms established with soils and sediments
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
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