Structure

10-Undecen-1-Ol

CAS
112-43-6
Catalog Number
ACM112436
Category
Fatty Alcohols
Molecular Weight
170.29
Molecular Formula
C11H22O

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Specification

Synonyms
10-Undecylenic alcohol
IUPAC Name
Undec-10-en-1-ol
SMILES
C=CCCCCCCCCCO
InChI
InChI=1S/C11H22O/c1-2-3-4-5-6-7-8-9-10-11-12/h2,12H,1,3-11H2
InChI Key
GIEMHYCMBGELGY-UHFFFAOYSA-N
Boiling Point
245-248 °C(lit.)
Melting Point
-3 °C
Flash Point
200 °F
Density
0.85 g/mL at 25 °C(lit.)
Solubility
Miscible with alcohol and ether; immiscible with water
Appearance
Clear colorless liquid
Storage
Inert atmosphere, room temperature
Active Content
95%
Alcohol
10-Undecenol
Assay
0.98
Bond Position Cis Trans
∆ 10
CNo Chain
C11:1
Complexity
89
Exact Mass
170.167065321
Monoisotopic Mass
170.167065321
Packaging
1 kg
Physical State
Liquid
pKa
15.20±0.10(Predicted)
Refractive Index
n20/D 1.45(lit.)
Stability
Stable. Incompatible with strong acids, strong oxidizing agents.
Storage Conditions
Inert atmosphere,Room Temperature
Topological Polar Surface Area
20.2 Ų
What is the IUPAC name of 10-Undecen-1-Ol?

The IUPAC name of 10-Undecen-1-Ol is Undec-10-en-1-ol.

What is the CAS number of 10-Undecen-1-Ol?

The CAS number of 10-Undecen-1-Ol is 112-43-6.

What is the molecular weight of 10-Undecen-1-Ol?

The molecular weight of 10-Undecen-1-Ol is 170.29.

What is the molecular formula of 10-Undecen-1-Ol?

The molecular formula of 10-Undecen-1-Ol is C11H22O.

What is the boiling point of 10-Undecen-1-Ol?

The boiling point of 10-Undecen-1-Ol is 132-133 °C.

What is the melting point of 10-Undecen-1-Ol?

The melting point of 10-Undecen-1-Ol is -3 °C.

What is the flash point of 10-Undecen-1-Ol?

The flash point of 10-Undecen-1-Ol is 200 °F.

What is the purity of 10-Undecen-1-Ol?

The purity of 10-Undecen-1-Ol is 95%+.

What is the density of 10-Undecen-1-Ol at 25°C?

The density of 10-Undecen-1-Ol at 25°C is 0.85 g/mL.

What are some typical applications of 10-Undecen-1-Ol?

Some typical applications of 10-Undecen-1-Ol include use as a dispersing agent, emulsifying agent, lubricant, and intermediate in organic synthesis.

Downstream Synthesis Route 1

  • 112-43-6
  • 53463-68-6

Reference: [1] Bioorganic and Medicinal Chemistry, 2011, vol. 19, # 11, p. 3527 - 3539

Downstream Synthesis Route 2

  • 112-43-6
  • 7766-50-9

Reference: [1] Synthetic Communications, 1984, vol. 14, # 7, p. 591 - 598

Downstream Synthesis Route 3

  • 112-43-6
  • 74036-98-9
  • 7766-50-9

Reference: [1] Helvetica Chimica Acta, 1926, vol. 9, p. 1086

Downstream Synthesis Route 4

  • 112-43-6
  • 112-42-5

Reference: [1]Kobayashi, Juta; Mori, Yuichiro; Kobayashi, Shu
[Chemical Communications, 2005, # 20, p. 2567 - 2568]

Downstream Synthesis Route 5

  • 112-43-6
  • 112-44-7

Reference: [1]Landini, Dario; Rolla, Franco
[Journal of Organic Chemistry, 1980, vol. 45, # 17, p. 3527 - 3529]
[2]Chuit et al.
[Helvetica Chimica Acta, 1926, vol. 9, p. 1086]
[3]Chuit et al.
[Helvetica Chimica Acta, 1926, vol. 9, p. 1086]
[4]Chuit et al.
[Helvetica Chimica Acta, 1926, vol. 9, p. 1086]

Downstream Synthesis Route 6

  • 112-43-6
  • 872-17-3

Reference: [1]Bergbreiter, David E.; Chandran, Rama
[Journal of the American Chemical Society, 1985, vol. 107, # 16, p. 4792 - 4793]
[2]Hoffmann, H. M. R.; Koever, Andreas; Pauluth, Detlef
[Journal of the Chemical Society. Chemical communications, 1985, # 12, p. 812 - 814]
[3]Bouveault
[Bulletin de la Societe Chimique de France, 1908, vol. <4> 3, p. 123]

* For details of the synthesis route, please refer to the original source to ensure accuracy.

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