Shopping on line can be easy, simple and save you lots of money. It can also take a lot of your time, frustrate you, and result in unwanted purchases. Now the same can be said for regular high street shopping, but with the vast opportunity presented by the Internet it will pay you to spend a few minutes reading this and understanding how to better optimize your Butanol shopping experience:
1. Compare - without doubt the biggest advantage that the Butanol offers shoppers today is the ability to compare thousands of Butanol at a time. This is a great thing, but not necessarily all the time! Too much can be daunting at times so take advantage of the great comparison sites and where possible let them do the hard work for you.
2. Research - if it has been said it will be on the internet. Ignorance is no longer a justifiable reason for buying the wrong thing. Take the time to research in detail everything that you could possible want to know about
3. Testimonials - don't know anybody that has bought a Butanol? Wrong! If the Butanol is good the internet will let you know. Use the Internet as a friend and get testimonials before you buy.
4. Questions - Got a question about Butanol then search the Forums, FAQ's, Blogs etc. Don't be afraid to ask .....
5. Reputation - Never heard of the company selling Butanol? Don't worry, no reason why you should know every company in the world, but you know someone that does! Use the internet to find out what people are saying about Butanol and build up a picture of their reputation for sales, returns, customer service, delivery etc.
6. Returns - still worried that even after all of the above your Butanol wont be what you want? Check out the returns policy. There is so much competition now that someone, somewhere is bound to offer the terms that you are comfortable with.
7. Feedback - happy with your Butanol then let people know, after all you are depending on others people input in your buying decision, so why not give a little back.
8. Security - check for the yellow padlock on the Butanol site before you buy, and the s after http:/ /i.e. https:// = a secure site
9. Contact - got a question about Butanol, or want to leave a comment then check out the sites contact page. Reputable companies have them and respond.
10. Payment - ready to pay for your Butanol, then use your credit card or PayPal! Be aware of companies that don't accept them, there may be genuine reasons but given the huge amount of choice you have when buying online there is no reason at all not to buy via credit card or PayPal.
{| class="toccolours" border="1" style="float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;"! | Butanol|-| align="center" colspan="2" bgcolor="#ffffff" |
|-! | General|-|
IUPAC nomenclature| 1-Butanol|-| Other names| Butanol
Butan-1-ol
n-Butanol
normal-Butanol
Butyl alcohol
Butyric alcohol
Propylcarbinol|-| Chemical formula| C4H10O|-| Simplified molecular input line entry specification| CCCCO|-| Molar mass| |-! | Properties|-| [Density and Phase (matter)| 0.8098 g/cm³ @ 20 °C, liquid|-| Solubility in Water (molecule)| 9.1 mL/100 mL H2O at 25 °C|-|-! | Structure|-| Orbital hybridisation#Molecule shape | ? |-| Coordination geometry | ? |-|
Crystal structure ],
monoclinic, orthorhombic, hexagonal,
rhombohedral, tetragonal,
cubic, and mention "close packed" or similar. You may also cite what class it belongs to, e.g. Cadmium_chloride#Crystal_structure -->|-|
Dipole#Molecular dipoles| 1.52
Debye (1-butanol)|-! | Hazards |-|
Material safety data sheet| External MSDS|-| Main
Worker safety and healths| flammable|-|
NFPA 704| 37 °C (99 °F)|-| [Risk and Safety Statements|
List of R-phrases:
List of S-phrases:
|-| RTECS number]|-|
Butanol (data page)#Structure and properties|
Refractive index,
Dielectric constant, etc.|-|
Butanol (data page)#Thermodynamic properties| Phase behaviour
Solid, liquid, gas|-|
Butanol (data page)#Spectral data|
UV/VIS spectroscopy,
Infrared spectroscopy,
nuclear magnetic resonance spectroscopy, Mass spectrometry|-! | Related compounds|-| Related
alcohols], Pentanol,
Isobutanol,
2-Butanol,
tert-Butanol, [Butyric acid,
Butylene
[wikipedia:Chemical infobox|-|}
Butanol or butyl alcohol (sometimes also called
biobutanol when produced biologically), is a primary
alcohol with a 4 carbon structure and the
molecular formula of
Carbon4Hydrogen10Oxygen. It is primarily used as a solvent, as an intermediate in chemical synthesis, and as a fuel. There are four
isomeric structures for butanol.
Isomers
The unmodified term
butanol usually refers to the straight chain isomer with the alcohol
functional group at the terminal carbon, which is also known as
n-butanol or 1-butanol. The straight chain isomer with the alcohol at an internal carbon is
sec-butanol or 2-butanol. The branched isomer with the alcohol at a terminal carbon is
isobutanol; 2-methyl-1-propanol, and the branched isomer with the alcohol at the internal carbon is
tert-butanol; 2-methyl-2-propanol.
{]|
isobutanol|}
Butanol isomers, due to their different structures, have somewhat different melting and boiling points. All are moderately miscible in water, less so than [ethanol, and more so than the higher (longer carbon chain) alcohols. This is because all alcohols have a hydroxyl group which makes them polar which in turn tends to promote solubility in water. At the same time the carbon chain of the alcohol resists solubility in water. Methanol, ethanol and propanol, are fully miscible in water because the hydroxyl group predominates while butanol is moderately miscible because of the balance between the two opposing solubility trends. Like many alcohols, butanol is toxic.
Uses
Biobutanol
Butanol is considered as a potential
biofuel (butanol fuel). Butanol at 85 percent strength can be used in cars without any change to the engine (unlike ethanol) and it produces more power than ethanol and almost as much power as gasoline.
Other uses
Butanol sees use as a
solvent for a wide variety of chemical and textile processes, in organic synthesis and as a chemical intermediate. It is also used as a
paint thinner and a solvent in other coating applications where it is used as a relatively slow evaporating latent solvent in lacquers and ambient-cured enamels. It finds other uses such as a component of
hydraulic fluid and brake fluids. Isobutanol at chemicalland21.com
It is also used as a base for
perfumes, but on its own has a highly alcoholic aroma.
Salts of butanol are chemical intermediates for example
alkali metal salts of tert-butanol are
tert-butoxides.
Production
Since the 1950s, most butanol in the
United States is produced commercially from fossil fuels. The most common process starts with
propene, which is run through an
hydroformylation reaction to form butanal, which is then reduced with hydrogen to butanol. Butanol can also be produced by
fermentation (biochemistry) of biomass by bacteria. Prior to the 1950s,
Clostridium acetobutylicum was used in industrial
fermentation (biochemistry) processes producing butanol. Research in the past few decades showed results of other microorganisms that can produce butanol through
fermentation (biochemistry).
See also
References
- Merck Index, 12th Edition, 1575.
{| class="toccolours" border="1" style="float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;"! | Butanol|-| align="center" colspan="2" bgcolor="#ffffff" |
|-! | General|-|
IUPAC nomenclature| 1-Butanol|-| Other names| Butanol
Butan-1-ol
n-Butanol
normal-Butanol
Butyl alcohol
Butyric alcohol
Propylcarbinol|-| Chemical formula| C4H10O|-|
Simplified molecular input line entry specification| CCCCO|-|
Molar mass| |-! | Properties|-| [Density and
Phase (matter)| 0.8098 g/cm³ @ 20 °C, liquid|-|
Solubility in
Water (molecule)| 9.1 mL/100 mL H2O at 25 °C|-|-! | Structure|-| Orbital hybridisation#Molecule shape | ? |-|
Coordination geometry | ? |-|
Crystal structure ],
monoclinic,
orthorhombic,
hexagonal, rhombohedral,
tetragonal, cubic, and mention "close packed" or similar. You may also cite what class it belongs to, e.g.
Cadmium_chloride#Crystal_structure -->|-| Dipole#Molecular dipoles| 1.52
Debye (1-butanol)|-! | Hazards |-|
Material safety data sheet| External MSDS|-| Main Worker safety and healths| flammable|-| NFPA 704| 37 °C (99 °F)|-| [Risk and Safety Statements| List of R-phrases:
List of S-phrases:
|-| RTECS number]|-| Butanol (data page)#Structure and properties| Refractive index,
Dielectric constant, etc.|-|
Butanol (data page)#Thermodynamic properties| Phase behaviour
Solid, liquid, gas|-|
Butanol (data page)#Spectral data|
UV/VIS spectroscopy,
Infrared spectroscopy,
nuclear magnetic resonance spectroscopy,
Mass spectrometry|-! | Related compounds|-| Related alcohols],
Pentanol,
Isobutanol, 2-Butanol,
tert-Butanol, [Butyric acid,
Butylene
[wikipedia:Chemical infobox|-|}
Butanol or butyl alcohol (sometimes also called
biobutanol when produced biologically), is a primary
alcohol with a 4
carbon structure and the
molecular formula of
Carbon4Hydrogen10
Oxygen. It is primarily used as a solvent, as an intermediate in chemical synthesis, and as a fuel. There are four
isomeric structures for butanol.
Isomers
The unmodified term
butanol usually refers to the straight chain isomer with the alcohol
functional group at the terminal carbon, which is also known as
n-butanol or 1-butanol. The straight chain isomer with the alcohol at an internal carbon is
sec-butanol or
2-butanol. The branched isomer with the alcohol at a terminal carbon is
isobutanol; 2-methyl-1-propanol, and the branched isomer with the alcohol at the internal carbon is
tert-butanol; 2-methyl-2-propanol.
{]|
isobutanol|}
Butanol isomers, due to their different structures, have somewhat different melting and boiling points. All are moderately miscible in water, less so than [ethanol, and more so than the higher (longer carbon chain) alcohols. This is because all alcohols have a hydroxyl group which makes them polar which in turn tends to promote solubility in water. At the same time the carbon chain of the alcohol resists solubility in water. Methanol, ethanol and propanol, are fully miscible in water because the hydroxyl group predominates while butanol is moderately miscible because of the balance between the two opposing solubility trends. Like many alcohols, butanol is toxic.
Uses
Biobutanol
Butanol is considered as a potential biofuel (
butanol fuel). Butanol at 85 percent strength can be used in cars without any change to the engine (unlike ethanol) and it produces more power than ethanol and almost as much power as gasoline.
Other uses
Butanol sees use as a solvent for a wide variety of chemical and textile processes, in organic synthesis and as a chemical intermediate. It is also used as a
paint thinner and a solvent in other coating applications where it is used as a relatively slow evaporating latent solvent in lacquers and ambient-cured enamels. It finds other uses such as a component of hydraulic fluid and
brake fluids. Isobutanol at chemicalland21.com
It is also used as a base for perfumes, but on its own has a highly alcoholic aroma.
Salts of butanol are chemical intermediates for example alkali metal salts of tert-butanol are
tert-butoxides.
Production
Since the 1950s, most butanol in the
United States is produced commercially from
fossil fuels. The most common process starts with propene, which is run through an
hydroformylation reaction to form butanal, which is then reduced with
hydrogen to butanol. Butanol can also be produced by fermentation (biochemistry) of
biomass by bacteria. Prior to the 1950s,
Clostridium acetobutylicum was used in industrial fermentation (biochemistry) processes producing butanol. Research in the past few decades showed results of other microorganisms that can produce butanol through fermentation (biochemistry).
See also
References
- Merck Index, 12th Edition, 1575.
Butanol - Wikipedia, the free encyclopedia
Butanol or butyl alcohol (sometimes also called biobutanol when produced biologically), is a primary alcohol with a 4 carbon structure and the molecular formula of C 4 H 10 O.
Butanol fuel - Wikipedia, the free encyclopedia
Butanol may be used as a fuel in an internal combustion engine. Because its longer hydrocarbon chain causes it to be fairly nonpolar, it is more similar to gasoline than is ethanol ...
ButylFuel,LLC Main Page
Working to produce butanol using common agricultural feedstocks not only for use as a solvent, but as a fuel that can replace gasoline. Compares butanol to gasoline, future plans ...
Safety (MSDS) data for 1-butanol
Safety (MSDS) data for 1-butanol ... Glossary of terms on this data sheet. The information on this web page is provided to help you to work safely, but it is intended to be an ...
Chemical Safety Data: 1-butanol
Chemical Safety Data: 1-butanol ... Common synonyms: n-butanol, butanol, butyl alcohol, 1-butyl acohol, n-butyl alcohol, butan-1-ol
Butanol production for use as a Biofuel in Europe
Butanol is an alcohol that can be used as a transport fuel. It is a higher member of the series of straight chain alcohols with each molecule of butanol (C 4 H 10 O) containing ...
Definition: butanol dehydrogenase from Online Medical Dictionary
The Online Medical Dictionary is a searchable dictionary of definitions from medicine, science and technology.
Definition: butanol-extractable iodine from Online Medical Dictionary
The Online Medical Dictionary is a searchable dictionary of definitions from medicine, science and technology.
ButylFuel FAQ
Butanol, biobutanol ... Two sources: Sharon Haydu Sales Associate Ashland Chemicals 1842 Enterprise Pkwy Twinsburg, OH 44087
GCSE SCIENCE CHEMISTRY HIGH SCHOOL - Alcohol - Isomers - Butanol ...
gcsescience.com 38 ...