Yes - it's rubbing alcohol. But, no I would not use it on the printer as it is pretty strong stuff and might damage your printer elements.
2007-01-07 23:34:17
·
answer #1
·
answered by David B 5
·
0⤊
0⤋
Isopropyl alcohol (also isopropanol or rubbing alcohol) is a common name for propan-2-ol, a colorless, flammable chemical compound with a strong odor. It has the chemical formula CH3CHOHCH3, and is the simplest example of a secondary alcohol, where the alcohol carbon is attached to two other carbons. It is an isomer of propanol.
Sterilizing pads typically contain a 60-70% solution of isopropanol in water. Isopropyl alcohol is also commonly used as a cleaner and solvent in industry. It is also used as a gasoline additive for dissolving water or ice in fuel lines. Isopropanol is the main ingredient in rubbing alcohol. It is used as a disinfectant, and is a common solvent.
Isopropanol is a major ingredient in "dry-gas" fuel additive. In significant quantities, water is a problem in fuel tanks as it separates from the gasoline. If the engine tried to combust the water instead of gasoline serious engine problems could result, as water cannot be compressed by an engine (see hydrolock). The isopropanol does not remove the water from the gasoline. Rather, the isopropanol solubilizes the water in the gasoline. Once soluble, the water does not pose the same risk as insoluble water.
It is also a very good cleaning agent and often used for cleaning electronic devices such as contact pins (like those on ROM cartridges), magnetic tape deck and floppy disk drive heads, the lenses of lasers in optical disc drives (e.g. CD, DVD) and removing thermal paste from CPUs. It is also used to clean glass computer monitor screens (at some risk to the anti-reflection coating of the screen), and used by many music shops to give second-hand or worn records newer looking sheens. It cleans dry-erase boards very well and other unwanted ink related marks.
2007-01-08 07:36:34
·
answer #2
·
answered by rahul_rd2002 1
·
0⤊
0⤋
Isopropyl alcohol or isopropanol is a common name for 2-propanol, an alcohol which is the main component of rubbing alcohol. Its chemical structure is: Its formula is C3H8O or more descriptively, CH3.CHOH.CH3.
Artificial fatty alcohol. Used as an antiseptic, a solvent, a rubbing alcohol and as a source for acetone..
2007-01-10 03:09:50
·
answer #3
·
answered by Anonymous
·
0⤊
0⤋
You can find great information about isopropyl alcohol at http://en.wikipedia.org/wiki/Isopropyl_alcohol
Michael,
Get Professional Website within 3 to 4 Days at a Reasonable Price.
http://www.designsitepro.com/
2007-01-08 07:35:05
·
answer #4
·
answered by Anonymous
·
0⤊
1⤋
No! Just use rubbing alcohol....it IS isopropyl alcohol!
2007-01-08 07:30:57
·
answer #5
·
answered by misteri 5
·
0⤊
0⤋
it is your basic rubbing alcohol you get in the little white bottles at any drug store....you could use those forced air cans but i wouldnt use anything else but what the manufacturer recommeneds or it could void you warranty
2007-01-08 07:28:22
·
answer #6
·
answered by clevelandrocksgirl 3
·
0⤊
0⤋
Isopropyl alcohol
General
Systematic name Propan-2-ol
Other names 2-propanol, isopropanol,
Isopropyl alcohol
Molecular formula C3H8O
SMILES CC(O)C
Molar mass 60.10 g/mol
Appearance Colorless liquid
CAS number 67-63-0
Properties
Density and phase 0.785 g/cm3, liquid
Solubility in water Fully miscible
Solubility in brine Slightly soluble
In ethanol, ether
In acetone, toluene Fully miscible
Soluble
Melting point -89 °C (185 K)
Boiling point 82.3 °C (355 K)
Acidity (pKa) 16.5 for H on hydroxyl
Viscosity 2.86 cP at 15 °C
1.77 cP at 30 °C
Dipole moment 1.66 D (gas)
Hazards
MSDS External MSDS
Main hazards Flammable
NFPA 704
310
Flash point 12 °C
R/S statement R11 R36 R67
S7 S16 S24 S25 S26
RTECS number NT8050000
Supplementary data page
Structure and
properties n, εr, etc.
Thermodynamic
data Thermal Conductivity: 0.14 W/m-K
Specific Heat: 2.56 kJ/kg-K
Heat of Vaporization: 664 kJ/kg[1]
Spectral data UV, IR, NMR, MS
Related compounds
Related alcohols 1-propanol,
ethanol, 2-butanol
Other compounds acetone, propylene,
diisopropyl ether,
2-bromopropane
Except where noted otherwise, data are given for
materials in their standard state (at 25°C, 100 kPa)
Infobox disclaimer and references
Isopropyl alcohol (also isopropanol or rubbing alcohol) is a common name for propan-2-ol, a colorless, flammable chemical compound with a strong odor. It has the chemical formula CH3CHOHCH3, and is the simplest example of a secondary alcohol, where the alcohol carbon is attached to two other carbons. It is an isomer of propanol.
Contents [hide]
1 Uses
2 Chemistry
3 Safety
4 Medicine/Toxicology
5 References
6 External links
[edit] Uses
Sterilizing pads typically contain a 60-70% solution of isopropanol in water. Isopropyl alcohol is also commonly used as a cleaner and solvent in industry. It is also used as a gasoline additive for dissolving water or ice in fuel lines. Isopropanol is the main ingredient in rubbing alcohol. It is used as a disinfectant, and is a common solvent.
Isopropanol is a major ingredient in "dry-gas" fuel additive. In significant quantities, water is a problem in fuel tanks as it separates from the gasoline. If the engine tried to combust the water instead of gasoline serious engine problems could result, as water cannot be compressed by an engine (see hydrolock). The isopropanol does not remove the water from the gasoline. Rather, the isopropanol solubilizes the water in the gasoline. Once soluble, the water does not pose the same risk as insoluble water.
It is also a very good cleaning agent and often used for cleaning electronic devices such as contact pins (like those on ROM cartridges), magnetic tape deck and floppy disk drive heads, the lenses of lasers in optical disc drives (e.g. CD, DVD) and removing thermal paste from CPUs. It is also used to clean glass computer monitor screens (at some risk to the anti-reflection coating of the screen), and used by many music shops to give second-hand or worn records newer looking sheens. It cleans dry-erase boards very well and other unwanted ink related marks.
[edit] Chemistry
Isopropyl alcohol forms an azeotrope with water at 87.4% alcohol. It is impossible to dehydrate isopropanol further using standard distillation methods. For this reason, more expensive means, such as using a desiccant, are necessary for production of 100% isopropyl alcohol.
Being a secondary alcohol, isopropanol can be oxidised to the ketone acetone. This can be achieved using oxidising agents such as chromic acid, or by dehydrogenation of isopropanol over a heated copper catalyst:
(CH3)2CH-OH â (CH3)2C=O + H2
Isopropanol may be converted to 2-bromopropane using phosphorus tribromide, or dehydrated to propylene by heating with sulfuric acid. With sodium hydroxide and a halogen, or with sodium hypochlorite, it undergoes the haloform reaction. This means it would give a positive result for an iodoform test.
Isopropanol is often used as a hydride source in the Meerwein-Ponndorf-Verley reduction.
Like most alcohols, isopropyl alcohol reacts with active metals such as potassium to form alkoxides which can be called isopropoxides. The reaction with aluminium (initiated by a trace of mercury) is used to prepare the catalyst aluminium isopropoxide.
Isopropanol has a maximal absorbance at 204 nm in an ultraviolet-visible spectrum.
[edit] Safety
Isopropyl alcohol vapour is heavier than air and is highly flammable with a very wide combustible range. It should be kept away from heat and open flame. When mixed with air or other oxidizers it can explode through deflagration. [1]
Isopropyl alcohol is oxidized by the liver into acetone. Symptoms of isopropyl alcohol poisoning include flushing, headache, dizziness, CNS depression, nausea, vomiting, anesthesia, and coma. Use in well-ventilated areas and use protective gloves while using. Poisoning can occur from ingestion, inhalation, or absorption.
Long term application to the skin can cause defatting.
[edit] Medicine/Toxicology
Isopropyl alcohol is about twice as toxic as ethanol. Isopropyl alcohol does not cause an anion gap acidosis (like ethanol or methanol). It produces an elevated osmolal gap, but generally no abnormal anion gap (though this may be seen as a result of hypotension and lactic acidosis). Overdoses may cause a fruity, acetone-like odor on the breath.
[edit] References
^ Safety (MSDS) data for 2-propanol. Retrieved on 2006-09-28.
[edit] External links
Molview from bluerhinos.co.uk See Propan-2-ol in 3D
Safety (MSDS) data for 2-propanol
The US government's Occupational Safety and Health Administration's guidelines for isopropyl alcohol.
Links to external chemical sources.
2007-01-08 07:45:31
·
answer #7
·
answered by shanekeavy 5
·
0⤊
0⤋