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136948

5-Nonanone

98%

Synonym(s):

Dibutyl ketone, Valerone

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25 G

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About This Item

Linear Formula:
CH3(CH2)3CO(CH2)3CH3
CAS Number:
502-56-7
Molecular Weight:
142.24
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24848303
EC Number:
207-946-5
Beilstein/REAXYS Number:
1743583
MDL number:
MFCD00009484
Assay:
98%
Form:
liquid

Key Documents

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InChI key

WSGCRAOTEDLMFQ-UHFFFAOYSA-N

InChI

1S/C9H18O/c1-3-5-7-9(10)8-6-4-2/h3-8H2,1-2H3

SMILES string

CCCCC(=O)CCCC

assay

98%

form

liquid

Quality Level

100

refractive index

n20/D 1.419 (lit.)

bp

186-187 °C (lit.)

mp

−50 °C (lit.)

density

0.826 g/mL at 25 °C (lit.)

functional group

ketone

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1 of 4

This Item
V659H6511M67001
5-Nonanone 98%

Sigma-Aldrich

136948

5-Nonanone

Valerophenone 99%

Sigma-Aldrich

V659

Valerophenone

3-Heptanone 98%

Sigma-Aldrich

H6511

3-Heptanone

3-Methyl-2-pentanone 99%

Sigma-Aldrich

M67001

3-Methyl-2-pentanone

assay

98%

assay

99%

assay

98%

assay

99%

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

mp

−50 °C (lit.)

mp

-

mp

−39 °C (lit.)

mp

-

density

0.826 g/mL at 25 °C (lit.)

density

0.975 g/mL at 20 °C (lit.)

density

0.818 g/mL at 25 °C (lit.)

density

0.815 g/mL at 25 °C (lit.)

bp

186-187 °C (lit.)

bp

244-245 °C (lit.)

bp

146-149 °C (lit.)

bp

118 °C/758 mmHg (lit.)

form

liquid

form

-

form

-

form

-

Application

5-Nonanone can be used as a reactant to prepare:
  • 5-nonanketoxime by reacting with hydroxylamine in water.
  • 4-Nitro-2,6-dipropylphenol by treating with a solution of formyl nitroenamine in the presence of a base.

Biochem/physiol Actions

5-Nonanone induces clinical neuropathy in rats[1].

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

141.8 °F - closed cup

flash_point_c

61 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB5673
STBL3913
STBK7006
STBK2607
STBJ9738

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A convenient method for synthesizing modified 4-nitrophenols
Nakaike Y, et al.
The Journal of Organic Chemistry, 70(24), 10169-10171 (2005)
Techno-economic analysis of 5-nonanone production from levulinic acid.
Patel AD, et al.
Chemical Engineering Journal, 160(1), 311-321 (2010)
Development of a general Pd (II)-catalyzed intermolecular hydroalkoxylation reaction of vinylphenols by using a sacrificial alcohol as the hydride source
Zhang Y and Sigman MS
Organic Letters, 8(24), 5557-5560 (2006)
Controlling selectivity in the reaction network of aldoxime hydrogenation to primary amines
Gebauer-Henke E, et al.
Catalysis Science & Technology, 2(12), 2539-2548 (2012)
Controlling Selectivity in the Consecutive Reaction Network of Aldoxime Hydrogenation to Primary Amines.
Gebauer-Henke E, et al.
Catalysis Science & Technology, 2, 2539-2548 (2012)
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