
111-87-5
- Product Name:Octanol
- Molecular Formula:C8H18O
- Purity:99%
- Molecular Weight:130.23
Product Details;
CasNo: 111-87-5
Molecular Formula: C8H18O
Appearance: colourless liquid
Perfect Factory Offer Excellent quality Octanol 111-87-5 with Safe Shipping
- Molecular Formula:C8H18O
- Molecular Weight:130.23
- Appearance/Colour:colourless liquid
- Melting Point:-15 °C(lit.)
- Refractive Index:n20/D 1.429(lit.)
- Boiling Point:194.665 °C at 760 mmHg
- PKA:15.27±0.10(Predicted)
- Flash Point:81.111 °C
- PSA:20.23000
- Density:0.824 g/cm3
- LogP:2.33920
1-Octanol(Cas 111-87-5) Usage
Safety Profile |
Poison by intravenous route.Moderately toxic by ingestion. Mutation data reported. Askin irritant. Combustible liquid when exposed to heat orflame; can react with oxidizing materials. To fight fire, usewater foam, fog, alcohol foam, dry chemical, CO2 |
InChI:InChI=1/C8H18O/c1-2-3-4-5-6-7-8-9/h9H,2-8H2,1H3
111-87-5 Relevant articles
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-
Gingras,Waters
, p. 3508,3511 (1954)
-
2-pyridylsilyl group as a multifunctional 'phase tag' for solution phase synthesis
Yoshida, Jun-ichi,Itami, Kenichiro,Mitsudo, Koichi,Suga, Seiji
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Brown, Herbert C.,Sikorski, James A.,Kulkarni, Surendra U.,Lee, Hsiupu D.
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Ogawa, Haruo,Tensai, Koh,Taya, Kazuo,Chihara, Teiji
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Soderquist, John A.,Medina, Jesus R.,Huertas, Ramon
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Shimoda, Kei,Kubota, Naoji,Hamada, Hiroki,Yamane, Shin-Ya,Hirata, Toshifumi
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111-87-5 Process route
-
- 67-56-1
methanol

-
- 629-82-3
di-n-octyl ether

-
- 111-87-5
octanol

-
- 10022-28-3
1,1-dimethoxyoctane
Conditions | Yield |
---|---|
In acetic acid; for 5.4h; Yield given; electrolysis: platinum-plate anode, carbon-rod cathode, Bu4NBF4, 20 F/mol, 0.5 A, 20 V;
|
-
- 3208-43-3,4527-76-8
4-tetrahydrofuran-2-yl-butan-2-ol

-
- 1004-29-1
2-butanyltetrahydrofuran

-
- 111-87-5
octanol

-
- 629-82-3
di-n-octyl ether
Conditions | Yield |
---|---|
With ruthenium-carbon composite; 1-(4-butylcarboxylic acid)-3-(n-butyl)-imidazolium bis(trifluoromethylsulfonyl)imide; hydrogen; at 150 ℃; for 15h; under 90009 Torr; Reagent/catalyst; Ionic liquid;
|
58.6% 27.1% 9.1% |
With 1-(4-butylcarboxylic acid)-3-(n-butyl)-imidazolium bis(trifluoromethylsulfonyl)imide; hydrogen; at 150 ℃; for 15h; under 90009 Torr; Reagent/catalyst; Ionic liquid;
|
25.8% 44.9% 26.1% |
With N,N,N-tributyl-1-(4-butylsulfonic acid)-aminium bis(trifluoromethylsulfonyl)imide; hydrogen; at 150 ℃; for 15h; under 90009 Torr; Reagent/catalyst; Ionic liquid;
|
11.7% 41.5% 34.5% |
With 5 wt% ruthenium/carbon; hydrogen; at 150 ℃; for 15h; under 90009 Torr; Ionic liquid;
|
111-87-5 Upstream products
-
75-21-8
oxirane
-
3761-92-0
n-hexylmagnesium bromide
-
123-91-1
1,4-dioxane
-
60-29-7
diethyl ether
111-87-5 Downstream products
-
10020-43-6
2-octyloxyethanol
-
929-56-6
1-methoxyoctane
-
123080-90-0
C6H5B(O-n-C8H17)2
-
16436-00-3
octyl 3-oxobutanoate
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AEO-9
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