ChemicalBook > Product Catalog >Organic Chemistry >Hydrocarbons and derivatives >Acyclic hydrocarbons >Kerosene

Kerosene

Kerosene Structure
CAS No.
8008-20-6
Chemical Name:
Kerosene
Synonyms
KEROSINE;jp-5;KEROSENE OIL;jp-8;jeta;Kerosene(Technical);Avtur;nafta;jeta-1;coaloil
CBNumber:
CB6854421
Molecular Formula:
N/A
Molecular Weight:
0
MOL File:
Mol file
Modify Date:
2024/3/14 15:18:27

Kerosene Properties

Melting point 24-25 °C
Boiling point 175-325 °C(lit.)
Density 0.8 g/mL at 25 °C(lit.)
vapor density 4.5 (vs air)
vapor pressure 0.23 mm Hg ( 20 °C)
refractive index n20/D 1.436
Flash point 179 °F
storage temp. 2-8°C
form Liquid
color Light Yellow
Odor Characteristic; like fuel oil.
explosive limit 5%
Merck 14,5294
Dielectric constant 1.8(21℃)
Stability Stable. Flammable. Incompatible with strong oxidizing agents.
EPA Substance Registry System Kerosene (8008-20-6)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07,GHS08,GHS09
Signal word  Danger
Hazard statements  H304-H315-H336-H411
Precautionary statements  P261-P264-P273-P301+P310-P302+P352-P331
Hazard Codes  Xn,N,F
Risk Statements  65-67-62-51/53-48/20-38-11-40
Safety Statements  23-24-62-61-36/37-16
RIDADR  1223
OEB A
OEL TWA: 100 mg/m3
WGK Germany  3
RTECS  OA5500000
Autoignition Temperature 442 °F
HazardClass  3
PackingGroup  III
HS Code  27101919
Toxicity LD50 orally in rabbits: 28 ml/kg (Deichmann)
NFPA 704
2
2 0

Kerosene Chemical Properties,Uses,Production

Description

Kerosene is primarily derived from refined petroleum. Kerosene was discovered in 1853 by Abraham Gesner, a British physician, through an extraction process of inflammable liquid from asphalt, a waxy petroleum mixture. Kerosene, therefore, is often called coal or fuel oil because of its asphalt origins. Kerosene was the first material to be chemically extracted on a large commercial scale.

Chemical Properties

Kerosene is a white to pale yellow, mobile flammable, and combustible liquid. Kerosene (hydrodesulfurized) is a complex combination of hydrocarbons obtained from a petroleum stock by treating with hydrogen to convert organic sulfur to hydrogen sulfide, which is removed. Kerosene generally consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 150–290℃ (302–554°F).

Uses

In kerosene lamps, flares, and stoves; as degreaser and cleaner; Deobase formerly used as a solvent in cosmetics and in fly spray.

Production Methods

Kerosene is produced by direct fractionation of the “middle distillate fraction”. Individual kerosene composition varies widely, but consists mainly of linear and branched aliphatics, olefins, cycloparaffins, and aromatics in the C10–C16 range. For indoor heating fuels it is desirable to remove the olefins, aromatics, and sulfur compounds, because they promote the evolution of soot and sulfur oxides. For some purposes, highly refined or “deodorized” kerosene is manufactured by treatment with activated charcoal or by clay filtration and is generally less toxic than untreated kerosene.

General Description

A clear colorless to light amber liquid with a petroleum odor. Flash point 100°F. Less dense than water and insoluble in water. Vapors are heavier than air.

Air & Water Reactions

Highly flammable. Insoluble in water.

Reactivity Profile

Saturated aliphatic hydrocarbons, contained in Kerosene, may be incompatible with strong oxidizing agents like nitric acid. Charring of the hydrocarbon may occur followed by ignition of unreacted hydrocarbon and other nearby combustibles. In other settings, aliphatic saturated hydrocarbons are mostly unreactive. They are not affected by aqueous solutions of acids, alkalis, most oxidizing agents, and most reducing agents.

Hazard

Moderate fire risk, explosive limits in air 0.7–5.0%. Toxic by inhalation. Questionable carcinogen.

Health Hazard

Vapor causes slight irritation of eyes and nose. Liquid irritates stomach; if taken into lungs, causes coughing, distress, and rapidly developing pulmonary edema.

Chemical Reactivity

Reactivity with Water No reaction; Reactivity with Common Materials: No reactions; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.

Environmental Fate

Kerosene is composed of aliphatic hydrocarbons with 10–16 carbons per molecule and benzene and naphthalene derivatives. Because kerosene is a complex mixture of various hydrocarbon fractions, its transport and transformation in the environment are dependent on the environment fate of the individual hydrocarbons that comprise it. Kerosene can enter the environment because of its uses – engine fuels, domestic heating, pesticide, and solvent. Environmental releases of kerosene predominantly results in portioning to air. The halflife reaction is calculated to be 0.27–2.2 days. Photodegeneration is rapid in the air phase. Kerosene is expected to have low mobility and some immobility when released to soil. Volatilization does occur. Kerosene is biodegradable in soil, although some components of the mixture adhere strongly to the soil. Kerosene is also biodegradable in surface water. However, some components of the mixture may bioconcentrate in fish and other aquatic organisms. Hydrolysis is insignificant because kerosene lacks the functional groups that hydrolyze under environmental conditions.

Purification Methods

Stir it with conc H2SO4 until a fresh portion of acid remains colourless, then wash with water, dry with solid KOH and distil it in a Claisen flask. For more complete drying, the kerosene can be refluxed with Na, and distilled from Na.

Global( 112)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
Alfa Aesar 1 800 209 7001 Maharashtra, India 6913 58 Inquiry
Central Drug House(P) Ltd. 91-11-49404040 New Delhi, India 6160 58 Inquiry
Skand Oil And Petro Chemical 08047634003 Haryana, India 1 58 Inquiry
Ruhani Lubricants 08048609518 Ahmedabad, India 5 58 Inquiry
Henan Tianfu Chemical Co.,Ltd. +86-0371-55170693 +86-19937530512 China 21676 55 Inquiry
Xiamen AmoyChem Co., Ltd +86-592-6051114 +8618959220845 China 6387 58 Inquiry
Shaanxi Dideu Medichem Co. Ltd +86-029-81138252 +86-18789408387 China 2316 58 Inquiry
SIMAGCHEM CORP +86-13806087780 China 17367 58 Inquiry
Hefei TNJ Chemical Industry Co.,Ltd. 0551-65418671 China 34571 58 Inquiry
Aladdin Scientific +1-+1(833)-552-7181 United States 57511 58 Inquiry
straight-runkerosene straight-runkerosine ultrasene WAX-OUT CLEANING SOLUTION Kerosene (PetroleuM Distillate) AF 100 (pesticide) KEROSENE, LOW ODOR Kerosene-Dyed KEROSENE EP Kerosene Odorless JP-5SHALE-DERIVEDJETFUEL SHALE-DERIVEDJP-5JETFUEL JETFUELJP-5 DIESELFUELNO1 AVIATIONKEROSENE NAVYFUELJP-5 PETROLEUM-DERIVEDJP-5JETFUEL KEROSENECOMBUSTION Kerosene (on conversion to C) Kerosine (petroleum) Straight run kerosine kerosene, deodorised Glycogen 6-glucano Hydrolase Sweatening kerosene Petroleum ether, boiling range ca. 180-280°c Petroleum etherboiling range ca. 180-280°Cpure Petroleum ether,pure,boiling range ca. 180-280°C Kerosene, pure Kerosene 5g [8008-20-6] PetroleuM ether, boiling range ca. 180-280レ pure 1LT PetroleuM ether, boiling range ca. 180-280レ pure 5LT Avtur Avtur (pesticide) Bayol 35 Kerosene 5000 μg/mL in methylene chloride Kerosene 50000 μg/mL in methylene chloride Kerosene 〔Kerosine〕 KEROSENE KEROSENE WHITE aviationturbinefuel(non-specificname) coaloil coal-oil deobase deodorizedkerosene deodorizedkerosine deodourizedkerosene distillatefueloils,light(non-specificname) fueloil,[no.1] fueloilno1 jeta-1 jetfuel5 jetfuel8 jetfuela jetfuela-1 jetfueltypea jetkerosine(non-specificname) jp5jetfuel jp-5jetfuel jp-8jetfuel