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74250

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:
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.

Signal Word

Danger

Hazard Statements

H226,H304,H315,H336,H410

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 Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

87.8 °F - closed cup

Flash Point(C)

31.0 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
Adrian A Accurso et al.
The Journal of organic chemistry, 76(11), 4392-4395 (2011-05-07)
Sulfur-, selenium-, and nitrogen-containing compounds bearing leaving groups in the β-position undergo facile substitution chemistry enabled by anchimeric assistance. Here we provide direct comparisons between such systems in the rigid bicyclo[3.3.1]nonane framework easily derived from 1,5-cyclooctadiene. For a series of
Arif Baran et al.
The Journal of organic chemistry, 77(11), 5086-5097 (2012-05-23)
Transformation of cyclohexa-2,4-diene-1,2-diylbis(methylene) diacetate to various carbasugars is described. Photooxygenation of a cyclohexadiene derivative gave a bicyclicendoperoxide, which was reduced with thiourea to [2-[(acetyloxy)methyl]cyclohexa-2,4-dien-1-yl]methyl acetate. Epoxidation of the remaining double bond followed by epoxide ring-opening and hydrolysis of the acetate
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