

Introduction of Butane
Butane is a hydrocarbon with molecular formula C4H10. It is an alkane and found in gaseous state at room temperature. It was discovered by British Chemist Edward Frankland in 1849. Although its various properties were described by Edmund Ronalds who was an English Industrial chemist. He found butane in the crude petroleum and studied its properties.
In other words, we can define butane as a member of the paraffin hydrocarbon series (or alkane series) which has 4 carbon atoms and 10 hydrogen atoms. Butane is a saturated hydrocarbon as single bonds are found between all carbon atoms of butane.
Butane Structure
As we have discussed, the molecular formula of butane is C4H10. Its IUPAC name is butane. In the word butane, prefix ‘But’ stands for 4 carbon atoms present in butane and suffix ‘ane’ comes from the alkane series which represent that butane belongs from alkane homologous series and is saturated in nature. Butane can be easily represented by the general formula of alkanes which is CnH2n+2 where n = any positive integer or number of carbon atoms. For butane n = 4, on putting the value of ‘n’ in the general formula C4H2.4+2 = C4H10. Thus, butane is a saturated hydrocarbon (single bond between carbon atoms) with four carbon atoms and ten hydrogen atoms. Therefore, its structure will be as follows –
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Butane or n-butane has a linear chain structure and covalent bonds between C – C and C – H. Each carbon atom has 4 sigma bonds. So, each carbon atom is sp3 hybridized and has a tetrahedral shape.
Properties of Butane
Various physical properties of butane are listed below –
Its molecular formula is C4H10 and empirical formula is C2H5.
Boiling point of butane is -1 to 1℃.
It is highly flammable.
It is gas at room temperature and atmospheric pressure.
It is a colorless gas.
It has an odor like gasoline.
It can be easily liquified and liquified butane gas can be easily converted into vapor at room temperature.
Molar mass of butane is 58.124g/mol.
Its density is 2.48kg/m3 at 15℃.
It is very less soluble in water. Its solubility in water is 61mg per liter at 68℉.
Chemical Properties of Butane
Few chemical properties of butane are listed below
Reaction with oxygen – Butane reacts with oxygen and forms carbon dioxide and water vapor. Reaction is given below -
2C4H10 + 13O2 🡪 8CO2 + 10H2O + Energy
If the amount of oxygen is limited, then it forms carbon monoxide and water vapor. Reaction is given below –
2C4H10 + 13O2 🡪 8CO2 + 10H2O
Reaction with chlorine – Butane reacts with chlorine and forms butyl chloride and HCl. Reaction is given below –
2C4H10 + Cl2 🡪 C4H9Cl + HCl
Reaction with iodine – Butane reacts with iodine and forms 2-iodobutane and hydrogen iodide. Reaction is given below –
2C4H10 + I2 🡪 C4H9I + HI
Production of Butane
Butane is a fossil fuel produced naturally by dead remains of the plants and animals deep inside the earth. It is found as natural gas deep inside the earth. We obtain butane by fractional distillation of crude oil. During this process we get many other products as well such as kerosene, diesel, heavy gas oil etc.
Fractional distillation is the process of separating various components of a liquid mixture on the basis of their different boiling points using a fractionating column. Fractional distillation of crude oil is also called petroleum refining.
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Uses of Butane
Butane is a fossil fuel and is very useful in many fields. Few of its applications are listed below
It is widely used as a fuel for various purposes.
It is one of the components of LPG (Liquified petroleum gas).
It is used for gasoline blending.
It is a key raw material of synthetic rubber.
Isobutane is used in refineries.
It is used in steam cracking.
It is used in deodorants or aerosol sprays as propellant.
It is used as fuel in cigarette lighters.
Its isomer isobutane is used in refrigerants.
It is used in air conditioning systems as well.
It is used as fuel in a butane torch as well.
It is used as fuel in camping stoves, barbecues etc. Although transportation of butane must be done very carefully.
Butane is not a greenhouse gas and does not produce smoke on burning. It does not affect the ozone layer of the atmosphere as well. Therefore, we can say, butane is an environmentally friendly gas or fuel.
Disadvantages of Butane: Is Butane Toxic to Humans?
As we discussed earlier, butane has numerous applications and makes our life easier. But it has some disadvantages as well. Although the toxicity of butane is very low, and its low or medium concentrations of butane exposure does not give any harmful effects. But exposure to its large concentrations can cause cardiac effects, cancer or central nervous system depression. Euphoria, drowsiness, unconsciousness, asphyxia etc. can be caused if you inhale butane. It may cause temporary memory loss, fluctuations in blood pressure or death. If it enters in the blood, then within seconds it causes intoxication. Burning of butane in a limited amount of oxygen forms carbon monoxide and prolonged inhalation of carbon monoxide may cause death. Contact of liquefied butane gas may cause permanent eye damage. It may cause itching of skin or numbness as well.
This ends our coverage on the topic “Butane”. We hope you enjoyed learning and were able to grasp the concepts. We hope after reading this article you will be able to solve problems based on the topic. If you are looking for solutions to NCERT Textbook problems based on this topic, then log on to Vedantu website or download Vedantu Learning App. By doing so, you will be able to access free PDFs of NCERT Solutions as well as Revision notes, Mock Tests and much more.
FAQs on Butane
1. What is the chemical formula and molecular structure of butane?
The chemical formula for butane is C₄H₁₀. Structurally, butane is an alkane, meaning it consists of carbon and hydrogen atoms connected by single bonds. The prefix 'but-' indicates it has four carbon atoms, which are linked in a chain. Each carbon atom is sp³ hybridized, resulting in a zigzag chain with a tetrahedral geometry around each carbon.
2. What are the main uses of butane in daily life and industry?
Butane is a versatile hydrocarbon with several common applications. Its primary uses include:
- Fuel: It is a major component of Liquefied Petroleum Gas (LPG) used for heating and cooking.
- Portable Fuel: It is the fuel used in cigarette lighters and portable camping stoves.
- Aerosol Propellant: It is used in products like deodorants and spray paints to propel the contents out of the can.
- Chemical Feedstock: It serves as a raw material for producing synthetic rubber and other organic chemicals.
3. How is butane related to LPG (Liquefied Petroleum Gas)?
Butane is one of the primary components of LPG. LPG is not a single compound but a flammable mixture of hydrocarbon gases, most commonly propane and butane. These gases are liquefied under moderate pressure for easy storage and transport. The specific ratio of propane to butane in LPG can vary depending on the region and climate.
4. What are the key differences between butane and butene?
Butane and butene are both hydrocarbons with four carbon atoms, but they differ significantly in their chemical structure and properties:
- Saturation: Butane (C₄H₁₀) is a saturated hydrocarbon (an alkane), meaning it only has single bonds between its carbon atoms. Butene (C₄H₈) is an unsaturated hydrocarbon (an alkene), containing one carbon-carbon double bond.
- Reactivity: The presence of the double bond makes butene more chemically reactive than the relatively inert butane.
- Hydrogen Atoms: Butane has 10 hydrogen atoms, while butene has 8, due to the presence of the double bond.
5. Why is butane a popular fuel for lighters and portable stoves?
Butane is ideal for portable applications like lighters and camping stoves because it can be easily liquefied under relatively low pressure. This allows a large amount of fuel to be stored in a small, lightweight canister. When the valve is opened, the pressure is released, and the liquid butane instantly vaporizes back into a flammable gas, ready for ignition.
6. How do butane and propane differ as common fuels, and when is one preferred?
The main practical difference between butane and propane lies in their boiling points. Propane has a much lower boiling point (-42°C) compared to butane (-1°C). This means propane will continue to vaporize and function as a gas in very cold conditions, making it the preferred choice for outdoor activities in winter. Butane can struggle to vaporize below freezing, making it more suitable for indoor or milder weather conditions.
7. How does the sp³ hybridization of carbon atoms determine the structure of butane?
In butane, every carbon atom undergoes sp³ hybridization, where one s-orbital and three p-orbitals mix to form four equivalent hybrid orbitals. These orbitals arrange themselves in a tetrahedral geometry around each carbon atom, with bond angles of approximately 109.5°. This tetrahedral arrangement at each carbon atom in the chain results in the overall molecule having a zigzag shape rather than a straight, linear one.
8. What are the structural isomers of butane, and how do their properties differ?
Butane has two structural isomers, which are compounds with the same molecular formula (C₄H₁₀) but different structural arrangements:
- n-butane: A straight-chain alkane where all four carbon atoms are arranged in a continuous chain.
- Isobutane (2-methylpropane): A branched-chain alkane with three carbons in the main chain and one methyl group attached to the central carbon.
9. Why is the incomplete combustion of butane considered hazardous?
When butane burns in a limited supply of oxygen (incomplete combustion), it produces carbon monoxide (CO) and soot (carbon) instead of the usual products of carbon dioxide (CO₂) and water. Carbon monoxide is a highly toxic gas that is colorless and odorless. If inhaled, it binds to haemoglobin in the blood more effectively than oxygen, leading to oxygen deprivation, which can be fatal. This is why proper ventilation is crucial when using butane-burning appliances.
10. What are the conformational isomers of butane, and why is the 'anti' form the most stable?
Conformational isomers, or conformers, are different spatial arrangements of a molecule that arise from rotation around a single C-C bond. For butane, the most notable conformers are the 'eclipsed,' 'gauche,' and 'anti' forms. The 'anti' conformation is the most stable because the two large methyl (-CH₃) groups at either end of the central C-C bond are positioned 180° apart from each other. This arrangement minimizes steric hindrance, which is the repulsive force between electron clouds of bulky groups, making it the lowest energy and most preferred state for the molecule.

















