Difference between revisions of "Limonene"

From CAMEO
Jump to navigation Jump to search
 
(5 intermediate revisions by 2 users not shown)
Line 1: Line 1:
 
== Description ==
 
== Description ==
  
A colorless solvent with a lemon-like odor that is occurs naturally from the oils of [[lemon oil|lemon]], orange, caraway, dill, and [[bergamot oil|bergamot]]. Limonene is used as a wetting and dispersing agent in liquid [[soap|soaps]], [[ink|inks]], perfumes, [[paint|paints]], [[varnish|varnishes]], floor waxes, and furniture polishes. It is also used as a solvent for [[alkyd resin|alkyd resins]], [[rosin]], [[wax|waxes]], and [[rubber, natural|rubber]] compounds.
+
A colorless solvent with a lemon-like odor that is occurs naturally from the oils of [[lemon oil|lemon]], orange, caraway, dill, and [[bergamot oil|bergamot]]. Limonene is used as a wetting and dispersing agent in liquid [[soap|soaps]], [[ink|inks]], perfumes, [[paint|paints]], [[varnish|varnishes]], floor waxes, and furniture polishes. It is also used as a solvent for [[alkyd resin|alkyd resins]], [[rosin]], [[wax|waxes]], and [[rubber|rubber]] compounds.
 +
[[[SliderGallery rightalign|limonene.jpg~Chemical structure]]]== Synonyms and Related Terms ==
  
== Synonyms and Related Terms ==
+
cinene; D-limonene; cajeputene; kautschin; dipentene (isomer mixture); Diene; carvene; 4-Isopropenyl-1-methylcyclohexene
  
cinene; D-limonene; cajeputene; kautschin; dipentene (isomer mixture); Diene; carvene; 4-Isopropenyl-1-methylcyclohexene
+
== Risks ==
  
[[[SliderGallery rightalign|limonene.jpg~Chemical structure]]]
+
* Skin contact will cause irritation. 
 +
* Flammable.  Flash point = 48C
 +
* ThermoFisher: [https://www.fishersci.com/shop/msdsproxy?productName=AC179390050&productDescription=(%2B)-LIMONENE+STABILI+97%25+5ML&catNo=AC17939-0050&vendorId=VN00032119&storeId=10652 SDS]
 +
* Most references consider limonene a green solvent because it is obtained often from food industry waste and biodegradable
  
== Other Properties ==
+
==Physical and Chemical Properties==
  
 
Miscible with ethanol. Insoluble in water.
 
Miscible with ethanol. Insoluble in water.
Line 22: Line 26:
 
|-
 
|-
 
! scope="row"| Melting Point
 
! scope="row"| Melting Point
| -75
+
| -75 C
 
|-
 
|-
 
! scope="row"| Density
 
! scope="row"| Density
| 0.8402
+
| 0.8402 g/ml
 
|-
 
|-
 
! scope="row"| Molecular Weight
 
! scope="row"| Molecular Weight
Line 34: Line 38:
 
|-
 
|-
 
! scope="row"| Boiling Point
 
! scope="row"| Boiling Point
| 175.5-176.5
+
| 175.5-176.5 C
 
|}
 
|}
  
== Hazards and Safety ==
+
== Resources and Citations ==
 
 
Skin contact will cause irritation.  Flammable.  Flash point = 48C
 
 
 
LINK: [http://www.cdc.gov/niosh/ipcsneng/neng0918.html International Chemical Safety Card]
 
 
 
== Authority ==
 
  
 
* Richard S. Lewis, ''Hawley's Condensed Chemical Dictionary'', Van Nostrand Reinhold, New York, 10th ed., 1993
 
* Richard S. Lewis, ''Hawley's Condensed Chemical Dictionary'', Van Nostrand Reinhold, New York, 10th ed., 1993

Latest revision as of 13:32, 17 April 2024

Description

A colorless solvent with a lemon-like odor that is occurs naturally from the oils of lemon, orange, caraway, dill, and bergamot. Limonene is used as a wetting and dispersing agent in liquid soaps, inks, perfumes, paints, varnishes, floor waxes, and furniture polishes. It is also used as a solvent for alkyd resins, Rosin, waxes, and Rubber compounds.

Chemical structure

Limonene.jpg

Synonyms and Related Terms

cinene; D-limonene; cajeputene; kautschin; dipentene (isomer mixture); Diene; carvene; 4-Isopropenyl-1-methylcyclohexene

Risks

  • Skin contact will cause irritation.
  • Flammable. Flash point = 48C
  • ThermoFisher: SDS
  • Most references consider limonene a green solvent because it is obtained often from food industry waste and biodegradable

Physical and Chemical Properties

Miscible with ethanol. Insoluble in water.

Composition C10H16
CAS 5989-27-5
Melting Point -75 C
Density 0.8402 g/ml
Molecular Weight mol. wt. = 136.23
Refractive Index 1.471
Boiling Point 175.5-176.5 C

Resources and Citations

  • Richard S. Lewis, Hawley's Condensed Chemical Dictionary, Van Nostrand Reinhold, New York, 10th ed., 1993
  • The Merck Index, Martha Windholz (ed.), Merck Research Labs, Rahway NJ, 10th edition, 1983 Comment: entry 5518
  • CRC Handbook of Chemistry and Physics, Robert Weast (ed.), CRC Press, Boca Raton, Florida, v. 61, 1980 Comment: ref. index=1.471