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Eicosane

HCID 8222
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Basic information

CAS
112-95-8
Standard SMILES
CCCCCCCCCCCCCCCCCCCC
InChIKey
CBFCDTFDPHXCNY-UHFFFAOYSA-N
Molecular formula
C20H42
Average molar mass
282.5 g/mol
Monoisotopic mass
282.32865134

Overview

N-eicosane appears as colorless crystals or white crystalline solid. (NTP, 1992)

Names & identifiers

Preferred name
Eicosane
IUPAC
icosane
English name
N-EICOSANE
Molecular formula
C20H42
Molecular weight
282.55

Names & synonyms

EICOSANEn-EicosaneIcosane112-95-83AYA9KEC48DIDECYLNSC-62789DTXSID1025227CHEBI:43619RefChem:5787DTXCID305227204-018-1
Show more names
n-IcosanN-EICOSANE STANDARD MATERIALNSC 62789ALKANE C20
Nonadecane, methyl-n-icosaneoctyldodecaneMFCD00009344PARAFOL 20ZNCIOpen2_003284Eicosane, analytical standardLFA

Database identifiers

CAS
112-95-8
PubChem CID
8222
DTXSID
DTXSID1025227
ChEBI
CHEBI:43619
UNII
3AYA9KEC48
EC Number
204-018-1
Nikkaji
J1.999B

Properties

Computed structural properties

XLogP
10.4
Topological polar surface area
0 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
0
Rotatable bonds
17
Heavy atoms
20
Formal charge
0
Complexity
132

Experimental & physicochemical properties

Chemical Classes · 2 items

Other Classes -> Aliphatics, Saturated (>C11)

n-Alkane

LipidsFatty Acyls [FA] -> Hydrocarbons [FA11]
FragrancesFragrance Ingredient (Eicosane) -> IFRA transparency List
OdorOdorless
Density · 2 items

0.7886 at 68 °F (NTP, 1992) - Less dense than water; will float

0.7886 g/cu cm at 20 °C

Color/Form · 2 items

Leaflets from alcohol

White crystalline solid

Solubility · 4 items

less than 1 mg/mL at 77 °F (NTP, 1992)

In water, 1.9X10-3 mg/L at 25 °C

Insoluble in water

Soluble in ether, petroleum ether, benzene; slightly soluble in chloroform; very soluble acetone

Flash Point · 2 items

212 °F (NTP, 1992)

> 113.00 °C (> 235.40 °F) - closed cup

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

GHS classification

GHS Classification · 5 items

This chemical does not meet GHS hazard criteria for 40.4% (116 of 287) of reports.

Danger

H304 (59.6%): May be fatal if swallowed and enters airways [Danger Aspiration hazard]

P301+P316, P331, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 287 reports by companies from 3 notifications to the ECHA C&L Inventory.

Hazard information

Regulatory Information · 4 items

Chemical: Eicosane

Eicosane is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Eicosane are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

REACH registered substance: Icosane (EC: 204-018-1)

Eicosane: Does not have an individual approval but may be used under an appropriate group standard

Other Safety InformationIMAP assessments - Eicosane: Human health tier I assessment
Fire HazardsThis chemical is combustible. (NTP, 1992)
Hazards SummaryThe commercial product is usually a mixture of primarily straight-chain hydrocarbons with an average of 20 carbons/molecule; [NTP] May cause irritation; [Acros Organics MSDS]
Reactive GroupHydrocarbons, Aliphatic Saturated
Reactivity Profile · 1 item

Saturated aliphatic hydrocarbons, such as N-EICOSANE, 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. When heated sufficiently or when ignited in the presence of air, oxygen or strong oxidizing agents, they burn exothermically to produce carbon dioxide and water.

Chemistry & industry

Pharmacology

Absorption, Distribution and Excretion · 2 items

Arthrobacter nicotianae KCC B35 isolated from blue-green mats densely covering oil sediments along the Arabian Gulf coast grew well on C10 to C40 n-alkanes as sole sources of carbon and energy. Growth on C20 to C40 alkanes was even better than on C10 to C18 alkanes. Biomass samples incubated for 6 hr with n-octacosane (C28) or n-nonacosane (C29) accumulated these compounds as the predominant constituent alkanes of the cell hydrocarbon fractions. The even chain hexadecane C16 and the odd chain pentadecane C15 were the second dominant constituent alkanes in C28 and C29 incubated cells, respectively. n-Hexadecane-incubated cells accumulated in their lipids higher proportions of C16-fatty acids than control cells not incubated with hydrocarbons. On the other hand, C28 and C29-incubated cells did not contain any fatty acids with the equivalent chain lengths, but the fatty acid patterns of the cell lipids suggest that there should have been mid-chain oxidation of these very long chain alkanes. This activity qualifies A. nicotianae KCC B35 to be used in cocktails for bioremediating environments polluted with heavy oil sediments.

Liver, heart, kidneys, muscle and adipose (perirenal and s.c.) /bovine/ tissues were collected from 6 animals for analysis of their hydrocarbon composition. Qualitative and quantitative determinations were carried out by gas chromatography and combined gas chromatography-mass spectrometry. Although differing in the proportions, a homologous series of n-alkanes ranging from n-C12-n-C31 was found in all samples. The isoprenoid hydrocarbons phytane and phytene (phyt-1-ene and phyt-2-ene) were also identified. (These findings have relevance to the health of humans consuming hydrocarbon-contaminated meats.) /n-Alkanes/

Cellular LocationsMembrane

Uses & manufacturing

Uses · 4 items

Used in cosmetics, lubricants, and plasticizers; [NTP]

Cosmetic, lubricants, plasticizers.

They are used mainly in applications for which isoalkanes are not acceptable for biological reasons, e.g., the production of detergents or proteins. /Higher n-Alkanes/

Solid n-alkanes (paraffin waxes) are used in a variety of applications, e.g., ... oxidation, and chlorination reactions. /Higher n-Alkanes/

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Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
Boiling Point · 3 items

648.9 °F at 760 mmHg (NTP, 1992)

344.1 °C

BP: 220 °C at 30 mm Hg

DecompositionHazardous decomposition products formed under fire conditions. - Carbon oxides
Melting Point · 2 items

98.1 °F (NTP, 1992)

36.48 °C

Vapor Density9.75 (NTP, 1992) - Heavier than air; will sink (Relative to Air)

Physicochemical properties

Melting point
35 · 35-37 °C(lit.)
Boiling point
220 °C30 · 220 °C30 mm Hg(lit.)
Density
0.7886 · 0.7886
vapor density
9.8 · 9.8 (vs air)
vapor pressure
0.001 hPa · <0.001 hPa (25 °C)
refractive index
1.4425 · 1.4425
Flash point
230 °F · >230 °F
storage temp.
30 °C · Store below +30°C.
solubility
100 mg/mL, · hexane: soluble100mg/mL, clear
form
Crystalline Solid
color
White
Odor
100 % · at 100.00%. waxy
Water Solubility
Soluble in ether, petroleum ether and benzene. Slightly soluble in acetone and chloroform. Insoluble in water.
BRN
1700722 · 1700722
Henry's Law Constant
5 · 5.0×10-6 mol/(m3Pa) at 25℃, Eastcott et al. (1988)
Stability
Stable. Combustible. Incompatible with strong oxidizing agents.
Cosmetics Ingredients Functions
FRAGRANCESOLVENTSKIN CONDITIONING - EMOLLIENTPERFUMING
InChI
1S/C20H42/c1-3-5-7-9-11-13-15-17-19-20-18-16-14-12-10-8-6-4-2/h3-20H2,1-2H3
InChIKey
CBFCDTFDPHXCNY-UHFFFAOYSA-N
SMILES
CCCCCCCCCCCCCCCCCCCC
LogP
11.46 at · 11.46 at 25℃
CAS DataBase Reference
112 · 112-95-8(CAS DataBase Reference)
Indirect Additives used in Food Contact Substances
EICOSANE
FDA 21 CFR
177.121 · 177.1210
EWG's Food Scores
1 · 1
FDA UNII
3 AYA9KEC48 · 3AYA9KEC48
EPA Substance Registry System
Eicosane (112-95-8)
UNSPSC Code
41116107 · 41116107
NACRES
24 · NA.24
Symbol(GHS)
8 · GHS08
Signal word
Danger
Hazard statements
304 · H304
Precautionary statements
301 · P301+P310-P331-P405-P501
PPE
95 · Eyeshields, Gloves, type N95 (US)
Hazard Codes
Xi
Risk Statements
36 · 36/37/38
Safety Statements
24 · 24/25-36/37-26
WGK Germany
3 · 3
TSCA
TSCA listed
HS Code
29011000 · 29011000
Storage Class
11 · 11 - Combustible Solids
Hazard Classifications
1 · Asp. Tox. 1
Hazardous Substances Data
112 · 112-95-8(Hazardous Substances Data)
REACH Registrations
Active
Air and Water ReactionsInsoluble in water.
Hazard Classes and CategoriesAsp. Tox. 1 (59.6%)
Skin, Eye, and Respiratory Irritations/Higher alkanes/ may cause eye and skin irritation.
Hazardous Reactivities and IncompatibilitiesIncompatible materials: Strong oxidizing agents.

Safety & protection

Fire FightingFires involving this material can be controlled with a dry chemical, carbon dioxide, or Halon extinguisher. (NTP, 1992)
First Aid · 1 item

EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.

Fire Fighting Procedures · 2 items

Suitable extinguishing media: Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.

Advice for firefighters: Wear self-contained breathing apparatus for firefighting if necessary.

Storage ConditionsKeep container tightly closed in a dry and well-ventilated place. Storage class (TRGS 510): Non Combustible Solids.
Cleanup Methods · 1 item

ACCIDENTAL RELEASE MEASURES Personal precautions, protective equipment and emergency procedures: Avoid dust formation. Avoid breathing vapors, mist or gas. Environmental precautions No special environmental precautions required. Methods and materials for containment and cleaning up: Sweep up and shovel. Keep in suitable, closed containers for disposal.

Nonfire Spill Response · 1 item

SMALL SPILLS AND LEAKAGE: If a spill of this chemical occurs, FIRST REMOVE ALL SOURCES OF IGNITION, then you should dampen the solid spill material with acetone and transfer the dampened material to a suitable container. Use absorbent paper dampened with acetone to pick up any remaining material. Seal your contaminated clothing and the absorbent paper in a vapor-tight plastic bag for eventual disposal. Solvent wash all contaminated surfaces with acetone followed by washing with a soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned.

Disposal Methods · 2 items

SRP: Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air quality; potential migration in air, soil or water; effects on animal, aquatic and plant life; and conformance with environmental and public health regulations. If it is possible or reasonable use an alternative chemical product with less inherent propensity for occupational harm/injury/toxicity or environmental contamination.

Product: Offer surplus and non-recyclable solutions to a licensed disposal company. Contaminated packaging: Dispose of as unused product.

Preventive Measures · 5 items

ACCIDENTAL RELEASE MEASURES Personal precautions, protective equipment and emergency procedures: Avoid dust formation. Avoid breathing vapors, mist or gas. Environmental precautions No special environmental precautions required.

Precautions for safe handling: Further processing of solid materials may result in the formation of combustible dusts. The potential for combustible dust formation should be taken into consideration before additional processing occurs. Provide appropriate exhaust ventilation at places where dust is formed.

Appropriate engineering controls: General industrial hygiene practice.

Gloves must be inspected prior to use. Use proper glove removal technique (without touching glove's outer surface) to avoid skin contact with this product. Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices. Wash and dry hands.

For more Preventive Measures (Complete) data for n-Eicosane (6 total), please visit the HSDB record page.

Personal Protective Equipment (PPE) · 5 items

RECOMMENDED RESPIRATOR: Where the neat test chemical is weighed and diluted, wear a NIOSH-approved half face respirator equipped with an organic vapor/acid gas cartridge (specific for organic vapors, HCl, acid gas and SO2) with a dust/mist filter. (NTP, 1992)

Eye/face protection: Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).

Handle with gloves.

Body Protection: Choose body protection in relation to its type, to the concentration and amount of dangerous substances, and to the specific work-place.

Respiratory protection: Respiratory protection is not required. Where protection from nuisance levels of dusts are desired, use type N95 (US) or type P1 (EN 143) dust masks. Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).

Toxicology

Environmental Fate · 3 items

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 5.9X10+5(SRC), determined from a structure estimation method(2), indicates that eicosane is expected to be immobile in soil(SRC). Volatilization of eicosane from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 90 atm-cu m/mole(SRC), using a fragment constant estimation method(3). However, adsorption to soil is expected to attenuate volatilization(SRC). Eicosane is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 4.62X10-6 mm Hg at 25 °C(4). Utilizing the Japanese MITI test, eicosane reached 89% of its Theoretical BOD in 4 weeks(5). Eicosane achieved 6 to 27% biodegradation after 28 days in sediment and marine-water inoculums(6), indicating that biodegradation is an important environmental fate process in soil.

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 5.9X10+5(SRC), determined from a structure estimation method(2), indicates that eicosane is expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces may occur(3) based upon an estimated Henry's Law constant of 90 atm-cu m/mole(SRC), using a fragment constant estimation method(4). Using this Henry's Law constant and an estimation method(3), volatilization half-lives for a model river and model lake are 1.7 hours and 6.7 days, respectively(SRC). However, adsorption to soil is expected to attenuate volatilization(SRC). The estimated volatilization half-life from a model pond is greater than 2 years if adsorption is considered(5). According to a classification scheme(6), an estimated BCF of 94(SRC), from an estimated log Kow of 10.16(2) and a regression-derived equation(2), suggests the potential for bioconcentration in aquatic organisms is moderate(SRC). Eicosane has a calculated half-life of 2.8 days(7) in unacclimated pond-water, indicating that biodegradation is an important environmental fate process under certain conditions in water.

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), eicosane, which has a vapor pressure of 4.62X10-6 mm Hg at 25 °C(2), will exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase eicosane is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 15 hours(SRC), calculated from its rate constant of 2.52X10-11 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). Particulate-phase eicosane may be removed from the air by wet and dry deposition(SRC). Eicosane does not contain chromophores that absorb at wavelengths >290 nm(4) and, therefore, is not expected to be susceptible to direct photolysis by sunlight(SRC).

Food Survey Values · 1 item

Eicosane was identified as a volatile component in the edible extract of Korean Chamchwi (Aster scaber Thunb)(1). Eicosane was detected in the extract of 6 out of 8 Australian yellow box honey samples, and 8 out of 8 Australian blue gum honey samples at average concentrations of 0.2 mg/kg and 0.1 mg/kg, respectively(2).

Toxicity Summary · 2 items

IDENTIFICATION AND USE: Eicosane is a solid n-alkane containing 20 carbon atoms (C20). It is used in cosmetic, lubricants, plasticizers. Solid n-alkanes (paraffin waxes) are also used as feeds for cracking them to gasoline blendstock materials, oxidation, and chlorination reactions. Recently, it has been reported that n-alkanes are principal components of diesel exhaust nanoparticles. HUMAN EXPOSURE AND TOXICITY: There are no data available. ANIMAL STUDIES: The addition of increasing amounts of eicosane to mouse surfactant increases surface compressibility at 30 mN/m during the second compression, suggesting that the deposition of alkane-rich nanoparticles onto pulmonary surfactants may be related to dysfunction of surfactant activity during breathing. A structure activity relationship of pure n-alkanes was undertaken in a mouse ear edema model to investigate the mechanism of cumulative irritancy. Alkanes were applied twice daily over a 4-day period. Hexadecane, octadecane, and eicosane exhibited progressively decreasing activity.

The existing information was reviewed by the independent Expert Panel for Fragrance Safety and supports the use of eicosane as described in this fragrance ingredient safety assessment. It is not genotoxic. Data from read-across analog heneicosane provide a calculated Margin of Exposure (MOE) greater than 100 for the repeated dose toxicity endpoint. Data from read-across analog undecanea provide a calculated Margin of Exposure (MOE) greater than 100 for the reproductive toxicity endpoint. Also, data from read-across analog paraffin wax show that there are no safety concerns for for skin sensitization under the current declared levels of use. Based on the lack of a chromophore, eicosane does not present a photoirritation/photoallergy concern. The local respiratory toxicity endpoint was evaluated using the Threshold of Toxicological Concern (TTC) for a Cramer Class I material, and the exposure is below the TTC.

Plant Concentrations · 2 items

Eiscosane detections in plants used in food and medicinal applications(1). /Eicosane/[Table#8365]

n-Eiscosane detections in plants used in food and medicinal applications(1).

Effluent Concentrations · 1 item

Eicosane was identified in the extract of some plastic materials from Concon, Chile(1); it was detected in the surface extract of new plastic bags, roadside litter, and landfill trash at concentrations of 55.9, 50.5, and 83.1 ug/g, respectively; it was detected in the particulate matter of open burn smoke from new plastic bags, roadside litter, and landfill trash, at concentrations of 9.2, 6.5, and 14.2 ng/mg, respectively; eicosane was detected in the surface extract and the open burn smoke of new plastic bags from the United States at a concentration of 123.2 ug/g and 65.0 ng/mg, respectively(1).

Soil Adsorption/Mobility · 1 item

The Koc of eicosane is estimated as 5.9X10+5(SRC), using an estimated log Kow of 10.16(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that eicosane is expected to be immobile in soil.

Natural Pollution SourcesEicosane is detected in various plants used in food and medicinal applications(1).
Atmospheric Concentrations · 2 items

URBAN/SUBURBAN: A mean ambient air concentration of 84.4 ng/cubic m was reported for eicosane from monitoring data measured on September 9, 1993 at Central Los Angeles, Azusa, and Claremont(1). In 2002, eicosane was detected in the gas-phase and the particulate-phase of urban and industrial air samples from Prato, Italy, at average concentrations of approximately 33.5 and 0.1 ng/cu m, respectively(2). Eicosane was detected in the particulate matter of ambient urban air sampled daily from January 2003 through December 2004 in Augsburg, Germany; average concentrations reported for spring, summer, fall and winter were 2.37, 0.41, 0.98, and 4.41 ng/cu m, respectively(3). During late fall and winter seasons eicoscane was monitored in the particulate matter of ambient atmospheres in urban areas of Corvallis OR, Guangzhou China, Beijing China, and Taiyuan China, with reported concentrations of not detected, 20.6, 102.1, and 25.2 ng/cu m, respectively(4).

SOURCE DOMINATED: Eicosane was detected in the gas and particle phase of tailpipe emissions from catalyst equipped gasoline powered motor vehicles at concentrations of 1.8 and 0.8 ug/km, respectively; and in the gas and particle phase of tailpipe emissions from non-catalyst equipped gasoline powered motor vehicles at concentrations of 100 and 190 ug/km, respectively; it was also detected in the gasoline at 2.5 ug/g(1). Average concentrations of eicosane emitted as a result of Chinese cooking styles were reported as 97, 65, 36, and 39 ng/mg, for Cantonese style, Sichuan style, Dongbei style, and Hunan style cooking, respectively(2).

Fish/Seafood Concentrations · 1 item

Barnacle samples collected from five locations in the Arabian Gulf had concentrations of eicosane ranging from not detected to 480 ng/g(1). Catfish samples collected from seven locations in the Arabian Gulf had concentrations of eicosane ranging from <0.1 to 14 ng/g(2).

Artificial Pollution Sources · 1 item

Alkanes such as eicosane may be components in petroleum products(1) and may be released to the environment through the processing and combustion of petroleum products(SRC). Eicosane's production and use in the manufacture of cosmetics, lubricants, and plasticizers(2) may result in its release to the environment through various waste streams.

Environmental Biodegradation · 1 item

AEROBIC: Eicosane, present at 100 mg/L, reached 89% of its theoretical BOD in 4 weeks using an activated sludge inoculum at 30 mg/L in the Japanese MITI test(1). Biodegradation of eicosane will occur under certain environmental conditions. Using a sediment sample and marine-water taken from Colgate Creek, Maryland (a relatively oil polluted environment), 27% eicosane was utilized by bacteria after 28 days; using a sediment sample and marine-water taken from Eastern Bay, Maryland (a relatively oil free environment), 6% eicosane was utilized by bacteria after 28 days; using the sediment sample from Colgate Creek in water taken from Eastern Bay, 22% eicosane was utilized by bacteria after 28 days; using a sediment sample from Eastern Bay and water from Colgate Creek, 11% eicosane was utilized by bacteria after 28 days(2). Eicosane, present as a component of Biodiesel, has a calculated half-life of 2.8 days, from examination of the primary aerobic biodegradation of commercial biodiesel fuel at 100 ppm, using unacclimated pond-water(3). Biodegradation of eicosane was measured by the biological oxygen demand using a suspension of Hudson-Collamer silt loam soil in water; oxidation of eicosane by microorganisms was achieved, resulting in 8.2 ug/mL oxygen consumed after 20 days(4).

Sediment/Soil Concentrations · 2 items

SEDIMENTS: Eicosane was detected in sediment samples from 14 sites along the Shinano River in Japan, from Nov 2005 to April 2006, at concentrations ranging from less than 0.2 to 22 ng/g(2).

SOIL: During winter 2002 soil and sand samples, from six locations in the Riyadh metropolitan area of Saudi Arabia, were examined for extractable organic matter; eicosane was detected at relative concentrations between 0.04 to 1.07% (of total extractable organic matter) at five of six locations(1).

Safety data

PPE
Eyeshields, Gloves, type N95 (US)
wgk
3
tsca
TSCA listed
hs_code
29011000
risk_code
36/37/38
Signal word
Danger
Symbol(GHS)
GHS08
hazard_code
Xi
safety_code
24/25-36/37-26
Storage Class
11 - Combustible Solids
Hazard statements
H304
REACH Registrations
Active
Hazard Classifications
Asp. Tox. 1
Precautionary statements
P301+P310-P331-P405-P501
Hazardous Substances Data
112-95-8(Hazardous Substances Data)
U.S. Production2021: 35,675 lb
Consumer UsesNot Known or Reasonably Ascertainable
Industry UsesNot Known or Reasonably Ascertainable
Methods of Manufacturing · 2 items

The liquefaction of coal provides the greatest variety of saturated hydrocarbons. The Fischer-Tropsch synthesis produces alkanes from syngas (CO + H2) in the range C1 to C30 or higher depending on the process variant: depending on the catalyst employed, the synthesis yields predominantly liquid hydrocarbons in the gasoline range, along with gases from C1 to C4 when iron-based catalysts are used, while cobalt-based catalysts produce longer chain hydrocarbons in the diesel and wax range that often undergo, depending of the desired product slate, further processing, especially for gasoline generation. While iron-based Fischer-Tropsch catalysts generate complex mixtures that also include branched and olefinic hydrocarbons, cobalt-based catalysts produce streams that are rich in n-alkanes and are therefore suitable raw materials for detergents and for wax products. /Saturated Hydrocarbons/

Suitable sources for n-alkanes with more than six carbon atoms are the appropriate petroleum distillate fractions, from which the n-paraffins can be isolated in high isomeric purity (= 95% linearity) by selective separation techniques, especially fractional distillation. /Higher n-Alkanes/

Formulations/PreparationsGrade: Pure normal (99+%), technical.
Use ClassificationFragrance Ingredients
General Manufacturing Information · 4 items

Not Known or Reasonably Ascertainable

Eicosane: ACTIVE

Recently, it has been reported that n-alkanes are principal components of diesel exhaust nanoparticles. /n-Alkanes/

Gas-phase dehydrogenation of n-alkanes over noble-metal catalysts yield the corresponding n-alkenes at low conversion rates (ca. 10%) with predominantly internal double bonds. The corresponding alkenes can be isolated in high purity by selective molecular-sieve processes. /Higher n-Alkanes/

Applications · 3 items

Usesn-Eicosane is a saturated aliphatic hydrocarbon, which is used to form candles and paraffin waxes with solar energy storage capacity. It is also used in cosmetics, lubricants, plasticizers and in the petrochemical industry. Further, it is useful for special surfactants and in the preparation of certain organic chemicals. In addition to this, it is used as a chromatographic analysis reference material.

UsesEicosane is a long chain saturated aliphatic hydrocarbon. Eicosane has a high flashpoint which makes it an inefficient fuel for use in the petrochemical industry. Eicosane is used to form candles and paraffin waxes with solar energy storage capacity.

General DescriptionColorless crystals or white crystalline solid.

Upstream & downstream products

Downstream products

Decane

Additional notes

DefinitionChEBI: Icosane is a straight chain alkane composed of 20 carbon atoms. It has been isolated from the leaves of Agave attenuata. It has a role as a plant metabolite.