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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:
Molecular Weight:
128.26
Beilstein:
1696917
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

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

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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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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The Journal of organic chemistry, 77(11), 5086-5097 (2012-05-23)
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Cesar A López et al.
Carbohydrate research, 364, 1-7 (2012-11-07)
The molecular dynamics simulation technique was used to study the folding and complexation process of a short amylose fragment in the presence of lipids. In aqueous solution, the amylose chain remains as an extended left-handed helix. After the addition of

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