Difference between revisions of "Camphor" - New World Encyclopedia

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{{Copyedited}}{{Images OK}}{{Submitted}}{{Approved}}
 
{{Chembox new
 
{{Chembox new
|   Reference=<ref>''The Merck Index'', 7th edition, Merk & Co, Rahway, New Jersey, USA, 1960</ref><ref>''Handbook of Chemistry and Physics'', CRC Press, Ann Arbor, Michigan</ref>
+
| Reference=<ref>Maryadele J. O'Neil (ed.), ''The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals'', 14th ed. (Whitehouse Station, NJ: Merck, ISBN 978-0911910001).</ref><ref>David R. Lide (ed.), ''CRC Handbook of Chemistry and Physics'', 88th ed.(Boca Raton, FL: CRC, 2007, ISBN 978-0849304880).</ref>
|   Name = Camphor
+
| Name = Camphor
|   ImageFile = camphor structure.png
+
| ImageFile = camphor structure.png
 
| ImageSize = 80px
 
| ImageSize = 80px
|   ImageName = Structure of camphor
+
| ImageName = Structure of camphor
|   IUPACName = 1,7,7-trimethylbicyclo<br /><nowiki>[2.2.1]heptan-2-one</nowiki>
+
| IUPACName = 1,7,7-trimethylbicyclo<br /><nowiki>[2.2.1]heptan-2-one</nowiki>
|   OtherNames = 2-bornanone, 2-camphanone<br />bornan-2-one, Formosa
+
| OtherNames = 2-bornanone, 2-camphanone<br />bornan-2-one, Formosa
 
| Section1 = {{Chembox Identifiers
 
| Section1 = {{Chembox Identifiers
|   SMILES = O=C1CC2CCC1(C)C2(C)(C)
+
| SMILES = O=C1CC2CCC1(C)C2(C)(C)
|   CASOther = [76-22-2] (unspecified)<br />[464-49-3] ((1''R'')-Camphor)<br />[464-48-2] ((1''S'')-Camphor}
+
| CASOther = [76-22-2] (unspecified)<br />[464-49-3] ((1''R'')-Camphor)<br />[464-48-2] ((1''S'')-Camphor}
|   RTECS = EX1260000 (''R'')<br />EX1250000 (''S'')
+
| RTECS = EX1260000 ''(R)''<br />EX1250000 ''(S)''
  }}
+
}}
 
| Section2 = {{Chembox Properties
 
| Section2 = {{Chembox Properties
|   Formula = C<sub>10</sub>H<sub>16</sub>O
+
| Formula = C<sub>10</sub>H<sub>16</sub>O
|   MolarMass = 152.23
+
| MolarMass = 152.23
|   Appearance = White or colorless crystals
+
| Appearance = White or colorless crystals
|   Density = 0.990 (solid)
+
| Density = 0.990 (solid)
|   Solubility = 0.12 [[gram|g]] in 100 ml
+
| Solubility = 0.12 [[gram|g]] in 100 ml
|   SolubilityOther = ~200 g in 100 ml
+
| SolubleOther = ~200 g in 100 ml
|   Solvent = acetic acid
+
| Solvent = acetic acid
|   SolubilityOther = ~100 g in 100 ml
+
| SolubilityOther = ~100 g in 100 ml
|   Solvent = ethanol
+
| Solvent = ethanol
|   SolubilityOther = ~250 g in 100 ml
+
| SolubilityOther = ~250 g in 100 ml
|   Solvent = acetone
+
| Solvent = acetone
|   Solvent = [[Diethyl ether|ether]]
+
| SolubleOther = ~100 g in 100 ml
|   SolubleOther = ~100 g in 100 ml
+
Solvent = [[Diethyl ether]]
SolubilityOther = ~200 g in 100 ml
+
| SolubilityOther = ~200 g in 100 ml
|   Solvent = chloroform
+
| Solvent = chloroform
|   MeltingPt = 179.75 °C (452.9 K)
+
| MeltingPt = 179.75 °C (452.9 K)
|   BoilingPt = 204 °C (477 K)
+
| BoilingPt = 204 °C (477 K)
|   pKa =  
+
| pKa =  
|   SpecRotation = +44.1°|(1''R'')-Camphor
+
| SpecRotation = +44.1°|(1''R'')-Camphor
  }}
+
}}
 
| Section7 = {{Chembox Hazards
 
| Section7 = {{Chembox Hazards
|   MainHazards = flammable
+
| MainHazards = flammable
|   EUClass =  
+
| EUClass =  
|   NFPA-H = 2
+
| NFPA-H = 2
|   NFPA-F = 2
+
| NFPA-F = 2
|   NFPA-R = 0
+
| NFPA-R = 0
|   RPhrases = 11-20/21/22-36/37/38
+
| RPhrases = 11-20/21/22-36/37/38
|   SPhrases = 16-26-36
+
| SPhrases = 16-26-36
  }}
+
}}
 
| Section8 = {{Chembox Related
 
| Section8 = {{Chembox Related
|   Function = ketone
+
| Function = ketone
|   OtherFunctn = [[fenchone]],[[thujone]]
+
| OtherFunctn = [[fenchone]],[[thujone]]
|   OtherCmpds = [[camphene]], [[pinene]]<br />[[borneol]], [[isoborneol]]<br />[[10-Camphorsulfonic acid]]
+
| OtherCmpds = [[camphene]], [[pinene]]<br />[[borneol]], [[isoborneol]]<br />[[10-Camphorsulfonic acid]]
  }}
+
}}
 
}}
 
}}
 +
'''Camphor''' is a waxy, white or transparent [[solid]] with a strong, aromatic odor.<ref>J. Mann, et al., ''Natural Products: Their Chemistry and Biological Significance'' (Harlow, Essex, UK: Longman Scientific & Technical, ISBN 0582060095), 309-311.</ref> Chemically, it is classified as a [[terpenoid]], and its [[chemical formula]] is [[carbon|C]]<sub>10</sub>[[hydrogen|H]]<sub>16</sub>[[oxygen|O]]. It is found in the [[bark]] and [[wood]] of the ''camphor laurel'' [[tree]] and other related trees of the laurel family. It can also be synthetically produced from oil of [[turpentine]]. It is used for its scent, as an ingredient in cooking (mainly in [[India]]), as an embalming fluid, and for medicinal purposes. It is also used in some religious ceremonies.
 +
{{toc}}
 +
If ingested in relatively large quantities, camphor is [[toxic|poisonous]], leading to [[seizure]]s, confusion, irritability, and even death.
  
'''Camphor''' is a waxy, white or transparent solid with a strong, aromatic odor.<ref>J. Mann, R. S. Davidson, J. B. Hobbs, D. V. Banthorpe, J. B. Harborne, ''Natural Products'', pp. 309-311, Addison Wesley Longman Ltd., Harlow, UK, 1994.  ISBN 0-582-06009-5</ref> It is a [[terpenoid]] with the [[chemical formula]] [[carbon|C]]<sub>10</sub>[[hydrogen|H]]<sub>16</sub>[[oxygen|O]].  It is found in wood of the '''camphor laurel''' (''[[Cinnamomum camphora]]''), a large [[evergreen]] tree found in Asia (particularly in [[Borneo]] and [[Taiwan]], hence its alternate name). It also occurs in some other related trees in the laurel family, notably ''[[Ocotea usambarensis]]''.  It can also be synthetically produced from oil of [[turpentine]]. It is used for its scent, as an ingredient in cooking (mainly in India), as an embalming fluid, in religious ceremonies and for medicinal purposes. A major source of camphor in Asia is [[Ocimum kilimandscharicum|camphor basil]].
+
== Etymology and history ==
  
==History==
+
The word camphor derives from the [[French language|French]] word ''camphre'', itself from Medieval [[Latin]] ''camfora'', from [[Arabic language|Arabic]] ''kafur'', from Malay ''kapur Barus'' meaning "Barus chalk." In fact Malay traders from whom Indian and Middle East merchants would buy camphor called it ''kapur'', "chalk" because of its white color.<ref>[http://www.etymonline.com/index.php?search=camphor&searchmode=none Camphor] ''Online Etymology Dictionary''. Retrieved June 11, 2008.</ref> Barus was the port on the western coast of the [[Indonesia|Indonesian]] island of [[Sumatra]] where foreign traders would call to buy camphor. In the Indian language [[Sanskrit]], the word ''karpoor'' is used to denote Camphore. An adaptation of this word, ''karpooram'', has been used for camphor in many South Indian ([[Dravidian languages|Dravidian]]) languages, such as [[Telugu language|Telugu]], [[Tamil language|Tamil]], [[Kannada language|Kannada]], and [[Malayalam language|Malayalam]].
The word camphor derives from the French word ''camphre'', itself from Medieval Latin ''camfora'', from Arabic ''kafur'', from Malay ''kapur Barus'' meaning "Barus chalk". In fact Malay traders from whom Indian and Middle East merchants would buy camphor called it ''kapur'', "chalk" because of its white colour [http://www.etymonline.com/index.php?search=camphor&searchmode=none]. Barus was the port on the western coast of the [[Indonesia|Indonesian]] island of [[Sumatra]] where foreign traders would call to buy camphor. In the Indian language Sanskrit, the word ''karpoor'' is used to denote Camphore. A South-Indian adaptation of this word, ''karpooram'', has been used for camphor in many South-Indian/[[Dravidian languages]] (like [[Telugu language|Telugu]], [[Tamil language|Tamil]], [[Kannada language|Kannada]] and [[Malayalam language|Malayalam]]).
 
  
 
Camphor was first synthesized by [[Gustaf Komppa]] in 1903. Previously, some organic compounds (such as [[urea]]) had been synthesized in the laboratory as a [[proof of concept]], but camphor was a scarce natural product with a worldwide demand. The synthesis was the first industrial [[total synthesis]], when Komppa began industrial production in [[Tainionkoski]], [[Finland]], in 1907.
 
Camphor was first synthesized by [[Gustaf Komppa]] in 1903. Previously, some organic compounds (such as [[urea]]) had been synthesized in the laboratory as a [[proof of concept]], but camphor was a scarce natural product with a worldwide demand. The synthesis was the first industrial [[total synthesis]], when Komppa began industrial production in [[Tainionkoski]], [[Finland]], in 1907.
  
'''Norcamphor''' is a camphor derivative with the three [[methyl]] groups replaced by hydrogen.
+
== Sources ==
  
Other substances deriving from trees are sometimes wrongly sold as camphor.
+
Camphor is extracted from the bark and wood of the camphor laurel ''([[Cinnamonum camphora]])'', a large [[evergreen]] tree found in [[Asia]], particularly, [[Borneo]] and [[Taiwan]]. It is also obtained from other related trees of the laurel family, notably ''[[Ocotea usambarensis]]'', and from the shrub known as ''camphor basil'' ''(Ocimum kilmandscharicum)''. Chemists have developed methods of synthesizing camphor from other compounds, such as from oil of [[turpentine]].
  
 +
Other substances derived from trees are sometimes wrongly sold as camphor.
  
==Uses==
+
== Properties ==
Modern uses include as a plasticizer for [[Nitrocellulose]], as a [[mothball|moth repellent]], as an antimicrobial substance, in embalming, and in [[fireworks]]. Solid camphor releases fumes that form a [[rust]]-preventative coating and is therefore stored in tool chests to protect tools against rust.<ref>[http://www.cabinetshoptips.com/ Tips for Cabinet Making Shops]</ref> Camphor crystals are also used to prevent damage to [[insect collecting|insect collections]] by other small insects.
 
  
It is also used in [[medicine]]. Camphor is readily absorbed through the skin and produces a feeling of cooling similar to that of [[menthol]] and acts as slight local [[anesthetic]] and [[antimicrobial]] substance. A form of [[antipruritic|anti-itch gel]] currently on the market uses camphor as its [[active ingredient]]. Camphor is an active ingredient (along with menthol) in vapor-steam products, such as [[Vicks]] VapoRub, and it is effective as a cough suppressant.  It may also be administered orally in small quantities (50 mg) for minor heart symptoms and fatigue.<ref>[http://spc.nam.fi/indox/english/html/nam/humspc/1/90151.shtml National Agency for Medicines]</ref>
+
Purified camphor takes the form of white or colorless [[crystal]]s, with a [[melting point]] of 179.75 °C (452.9 K) and a [[boiling point]] of 204 °C (477 K). It is poorly soluble in [[water]], but it is highly soluble in organic [[solvent]]s such as [[acetone]], [[acetic acid]], [[diethyl ether]], and [[chloroform]].
  
In the 18th Century, it was used by [[Leopold_Auenbrugger|Auenbrugger]] in the treatment of [[mania]].{{Fact|date=March 2007}}
+
'''Norcamphor''' is a camphor derivative with the three [[methyl]] groups replaced by [[hydrogen]] [[atom]]s.
  
It is also believed that camphor will deter snakes and other reptiles due to its strong odor. Similarly, camphor is believed to be toxic to insects and is thus sometimes used as a repellent.{{Fact|date=March 2007}}
+
=== Chemical reactions ===
  
Camphor is also used in the Mahashivratri celebrations of Shiva, the Hindu god of destruction of (re)creation. As a natural pitch substance it burns cool without leaving an ash residue, which symbolizes consciousness.
+
Camphor can undergo various reactions, some of which are given below.
  
It is also found in clarifying masks used for skin.
+
* [[Bromination]]:
 +
:[[Image:Camphor-3-Brominecampher.png|500px]]
  
Recently, [[carbon nanotubes]] were successfully synthesized using camphor in [[chemical vapor deposition]] process.<ref>Mukul Kumar, Yoshinori Ando, ''Carbon Nanotubes from Camphor: An Environment-Friendly Nanotechnology'', Journal of Physics: Conference Series 61 (2007) 643–646</ref>
+
* [[Oxidation]] with [[nitric acid]]:
 
+
:[[Image:Camphor-Camphor_acid.png]]
===Culinary===
 
Currently, camphor is mostly used as a flavoring for sweets in Asia. In ancient and medieval Europe it was widely used as ingredient for sweets but it is now mainly used for medicinal purposes. Camphor was used as a flavoring in confections resembling [[ice cream]] in [[China]] during the [[Tang dynasty]] (A.D. 618-907).{{Fact|date=June 2007}} Camphor is widely used in cooking (mainly for dessert dishes) in India where it is known as ''Pachha Karpooram'' (literally meaning "green camphor" though "Pachha" in Tamil can also be translated to mean "raw" which is "Pachha Karpooram's" intended meaning). It is widely available at Indian grocery stores and is labeled as "Edible Camphor." In Hindu [[pooja]]s and ceremonies, camphor is burned in a ceremonial spoon for performing [[aarti]]. This type of camphor is also sold at Indian grocery stores but it is not suitable for cooking. The only type that should be used for food are those which are labeled as "Edible Camphor."
 
  
==Toxicology==
+
* Conversion to isonitrosocamphor:
In larger quantities, it is [[toxic|poisonous]] when ingested and can cause seizures, confusion, irritability, and [[neuromuscular]] [[hyperactivity]]. In 1980, the [[United States]] [[Food and Drug Administration]] set a limit of 11% allowable camphor in consumer products and totally banned products labeled as camphorated oil, camphor oil, camphor [[liniment]], and camphorated liniment (but "white camphor [[essential oil]]" contains no significant amount of camphor). Since alternative treatments exist, medicinal use of camphor is discouraged by the FDA, except for skin-related uses, such as medicated powders, which contain only small amounts of camphor. Lethal doses in adults are in the range 50–500 mg/kg (orally). Generally, 2 g causes serious toxicity and 4 g is potentially lethal.
 
 
 
==Reactions==
 
Typical camphor reactions are:
 
* [[bromination]]
 
:[[Image:Camphor-3-Brominecampher.png|500px]]
 
* [[oxidation]] with [[nitric acid]]
 
:[[Image:Camphor-Camphor_acid.png]]
 
* conversion to isonitrosocamphor
 
 
:[[Image:Camphor-Isonitrosocamphor.png|550px]]
 
:[[Image:Camphor-Isonitrosocamphor.png|550px]]
  
Camphor can also be reduced to [[isoborneol]] using [[sodium borohydride]].
+
* Camphor can also be reduced to [[isoborneol]] using [[sodium borohydride]].
  
 
==Biosynthesis==
 
==Biosynthesis==
In [[biosynthesis]] camphor is produced from [[geranyl pyrophosphate]], via cyclisation of [[linalool|linaloyl]] pyrophosphate to [[Borneol|bornyl]] pyrophosphate, followed by hydrolysis to [[borneol]] and oxidation to camphor.
+
 
 +
In [[biosynthesis]], camphor is produced from [[geranyl pyrophosphate]]. The reactions involve cyclization of [[linalool|linaloyl]] pyrophosphate to [[Borneol|bornyl]] pyrophosphate, followed by hydrolysis to borneol and oxidation to camphor. The reactions may be written as shown below.
  
 
[[Image:CamphorBiosynthesis.png|700px|center|Biosynthesis of camphor from geranyl pyrophosphate]]
 
[[Image:CamphorBiosynthesis.png|700px|center|Biosynthesis of camphor from geranyl pyrophosphate]]
 +
 +
==Uses==
 +
 +
Currently, camphor is useful for a variety of applications. For instance, it is a [[mothball|moth repellent]], an antimicrobial agent, an embalming agent, and a component of [[fireworks]]. It is also added as a plasticizer for [[nitrocellulose]]. Solid camphor releases fumes that form a [[rust]]-preventative coating and is therefore stored in tool chests to protect tools against rust.<ref>[http://www.cabinetshoptips.com/ Keeping rust off your tools] Retrieved June 11, 2008.</ref> Camphor is believed to be toxic to [[insect]]s, and its crystals are used to prevent damage to [[insect collecting|insect collections]] by other small insects. The strong odor of camphor is thought to deter [[snake]]s and other [[reptile]]s.
 +
 +
Recently, [[carbon nanotubes]] were successfully synthesized using camphor by a [[chemical vapor deposition]] process.<ref>Mukul Kumar and Yoshinori Ando, Carbon Nanotubes from Camphor: An Environment-Friendly Nanotechnology, ''Journal of Physics'' Conference Series, (2007) 61: 643–646.</ref>
 +
 +
=== Medical uses ===
 +
 +
Camphor has several uses in [[medicine]]. It is readily absorbed through the skin and produces a cool feeling, similar to that of [[menthol]], and it acts as a slight local [[anesthetic]] and [[antimicrobial]] substance. A form of anti-itch gel ([[antipruritic]]) currently on the market uses camphor as its [[active ingredient]]. Camphor is an active ingredient (along with menthol) in vapor-steam products, such as [[Vicks]] VapoRub, and it is effective as a cough suppressant. It may also be administered orally in small quantities (50 mg) for minor heart symptoms and fatigue.<ref>Summaries of Product Characteristics (SPC) for Human medicinal products ''National Agency for Medicines'' (Finnish).</ref> Camphor is also used in clarifying masks used for the skin.
 +
 +
=== Culinary uses ===
 +
 +
Camphor was used as a flavoring in confections resembling [[ice cream]] in [[China]] during the [[Tang dynasty]] (C.E. 618-907). In ancient and medieval [[Europe]], it was widely used as an ingredient for sweets, but it is now mainly used for medicinal purposes in European countries. In [[Asia]], however, it continues to be used as a flavoring for sweets.
 +
 +
In [[India]], camphor is widely used in cooking, mainly for dessert dishes. In South India, it is known as ''Pachha Karpooram'', meaning "green camphor" or "raw camphor." (The latter appears to be the intended meaning, as translated from Tamil.) It is widely available at Indian grocery stores and is labeled as "Edible Camphor." The type of camphor used for Hindu ceremonies is also sold at Indian grocery stores, but it is not suitable for cooking. The only type that should be used for food is that labeled as "Edible Camphor."
 +
 +
=== Religious ceremonies ===
 +
 +
In [[Hinduism|Hindu]] worship ceremonies ([[pooja]]s), camphor is burned in a ceremonial spoon for performing [[aarti]]. It is used in the Mahashivratri celebrations of [[Shiva]], the Hindu god of destruction and re-creation. As a natural pitch substance, it burns cool without leaving an ash residue, which symbolizes consciousness.
 +
 +
==Toxicity==
 +
 +
In larger quantities, it is [[toxic|poisonous]] when ingested and can cause seizures, confusion, irritability, and [[neuromuscular]] [[hyperactivity]]. In 1980, the [[United States]] [[Food and Drug Administration]] set a limit of 11 percent allowable camphor in consumer products and totally banned products labeled as camphorated oil, camphor oil, camphor [[liniment]], and camphorated liniment (but "white camphor [[essential oil]]" contains no significant amount of camphor). Since alternative treatments exist, medicinal use of camphor is discouraged by the FDA, except for skin-related uses, such as medicated powders, which contain only small amounts of camphor. Lethal, orally ingested doses in adults are in the range 50–500 milligrams per kilogram (mg/kg) of body weight. Generally, two grams (g) causes serious toxicity and four grams is potentially lethal.
  
 
== See also ==
 
== See also ==
Line 107: Line 125:
  
 
==References==
 
==References==
 +
* Lide, David R. (ed.). 2007. ''CRC Handbook of Chemistry and Physics'', 88th ed. Boca Raton, FL: CRC. ISBN 978-0849304880
 +
* Mann, J., et al. 1994. ''Natural Products: Their Chemistry and Biological Significance''. Harlow, Essex, UK: Longman Scientific & Technical. ISBN 0582060095
 +
* O'Neil, Maryadele J. (ed.). 2006. ''The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals'', 14th ed. Whitehouse Station, NJ: Merck. ISBN 978-0911910001
 +
* Sell, Charles. 2003. ''A Fragrant Introduction to Terpenoid Chemistry.'' Cambridge: Royal Society of Chemistry. ISBN 978-0854046812
 +
* Smith, Michael, and Jerry March. 2001. ''March's Advanced Organic Chemistry: Reactions, Mechanisms, and Structure'', 5th ed. New York: Wiley. ISBN 978-0471585893
  
 
==External links==
 
==External links==
 
+
All links retrieved November 25, 2023.
*[http://www.naturaldatabase.com/ce/ceNDMono.aspx?mono_id=709&view=m Camphor Evidence-based Monograph] from ''Natural Medicines Comprehensive Database''
+
* [http://www.naturaldatabase.com/ce/ceNDMono.aspx?mono_id=709&view=m Camphor] ''Natural Medicines Comprehensive Database''.
 +
* [http://www.wisegeek.com/what-is-camphor.htm What is Camphor?] ''wiseGEEK''.
  
 
[[Category:Physical sciences]]
 
[[Category:Physical sciences]]

Latest revision as of 18:58, 25 November 2023


Camphor[1][2]
Camphor structure.png
IUPAC name 1,7,7-trimethylbicyclo
[2.2.1]heptan-2-one
Other names 2-bornanone, 2-camphanone
bornan-2-one, Formosa
Identifiers
CAS number [76-22-2] (unspecified)
[464-49-3] ((1R)-Camphor)
[464-48-2] ((1S)-Camphor}
RTECS number EX1260000 (R)
EX1250000 (S)
SMILES O=C1CC2CCC1(C)C2(C)(C)
Properties
Molecular formula C10H16O
Molar mass 152.23
Appearance White or colorless crystals
Density 0.990 (solid)
Melting point

179.75 °C (452.9 K)

Boiling point

204 °C (477 K)

Solubility in water 0.12 g in 100 ml
Solubility in chloroform ~100 g in 100 ml
Chiral rotation [α]D +44.1°
Hazards
Main hazards flammable
NFPA 704

NFPA 704.svg

2
2
0
 
R-phrases 11-20/21/22-36/37/38
S-phrases 16-26-36
Related Compounds
Related ketone fenchone,thujone
Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Camphor is a waxy, white or transparent solid with a strong, aromatic odor.[3] Chemically, it is classified as a terpenoid, and its chemical formula is C10H16O. It is found in the bark and wood of the camphor laurel tree and other related trees of the laurel family. It can also be synthetically produced from oil of turpentine. It is used for its scent, as an ingredient in cooking (mainly in India), as an embalming fluid, and for medicinal purposes. It is also used in some religious ceremonies.

If ingested in relatively large quantities, camphor is poisonous, leading to seizures, confusion, irritability, and even death.

Etymology and history

The word camphor derives from the French word camphre, itself from Medieval Latin camfora, from Arabic kafur, from Malay kapur Barus meaning "Barus chalk." In fact Malay traders from whom Indian and Middle East merchants would buy camphor called it kapur, "chalk" because of its white color.[4] Barus was the port on the western coast of the Indonesian island of Sumatra where foreign traders would call to buy camphor. In the Indian language Sanskrit, the word karpoor is used to denote Camphore. An adaptation of this word, karpooram, has been used for camphor in many South Indian (Dravidian) languages, such as Telugu, Tamil, Kannada, and Malayalam.

Camphor was first synthesized by Gustaf Komppa in 1903. Previously, some organic compounds (such as urea) had been synthesized in the laboratory as a proof of concept, but camphor was a scarce natural product with a worldwide demand. The synthesis was the first industrial total synthesis, when Komppa began industrial production in Tainionkoski, Finland, in 1907.

Sources

Camphor is extracted from the bark and wood of the camphor laurel (Cinnamonum camphora), a large evergreen tree found in Asia, particularly, Borneo and Taiwan. It is also obtained from other related trees of the laurel family, notably Ocotea usambarensis, and from the shrub known as camphor basil (Ocimum kilmandscharicum). Chemists have developed methods of synthesizing camphor from other compounds, such as from oil of turpentine.

Other substances derived from trees are sometimes wrongly sold as camphor.

Properties

Purified camphor takes the form of white or colorless crystals, with a melting point of 179.75 °C (452.9 K) and a boiling point of 204 °C (477 K). It is poorly soluble in water, but it is highly soluble in organic solvents such as acetone, acetic acid, diethyl ether, and chloroform.

Norcamphor is a camphor derivative with the three methyl groups replaced by hydrogen atoms.

Chemical reactions

Camphor can undergo various reactions, some of which are given below.

  • Bromination:
Camphor-3-Brominecampher.png
Camphor-Camphor acid.png
  • Conversion to isonitrosocamphor:
Camphor-Isonitrosocamphor.png
  • Camphor can also be reduced to isoborneol using sodium borohydride.

Biosynthesis

In biosynthesis, camphor is produced from geranyl pyrophosphate. The reactions involve cyclization of linaloyl pyrophosphate to bornyl pyrophosphate, followed by hydrolysis to borneol and oxidation to camphor. The reactions may be written as shown below.

Biosynthesis of camphor from geranyl pyrophosphate

Uses

Currently, camphor is useful for a variety of applications. For instance, it is a moth repellent, an antimicrobial agent, an embalming agent, and a component of fireworks. It is also added as a plasticizer for nitrocellulose. Solid camphor releases fumes that form a rust-preventative coating and is therefore stored in tool chests to protect tools against rust.[5] Camphor is believed to be toxic to insects, and its crystals are used to prevent damage to insect collections by other small insects. The strong odor of camphor is thought to deter snakes and other reptiles.

Recently, carbon nanotubes were successfully synthesized using camphor by a chemical vapor deposition process.[6]

Medical uses

Camphor has several uses in medicine. It is readily absorbed through the skin and produces a cool feeling, similar to that of menthol, and it acts as a slight local anesthetic and antimicrobial substance. A form of anti-itch gel (antipruritic) currently on the market uses camphor as its active ingredient. Camphor is an active ingredient (along with menthol) in vapor-steam products, such as Vicks VapoRub, and it is effective as a cough suppressant. It may also be administered orally in small quantities (50 mg) for minor heart symptoms and fatigue.[7] Camphor is also used in clarifying masks used for the skin.

Culinary uses

Camphor was used as a flavoring in confections resembling ice cream in China during the Tang dynasty (C.E. 618-907). In ancient and medieval Europe, it was widely used as an ingredient for sweets, but it is now mainly used for medicinal purposes in European countries. In Asia, however, it continues to be used as a flavoring for sweets.

In India, camphor is widely used in cooking, mainly for dessert dishes. In South India, it is known as Pachha Karpooram, meaning "green camphor" or "raw camphor." (The latter appears to be the intended meaning, as translated from Tamil.) It is widely available at Indian grocery stores and is labeled as "Edible Camphor." The type of camphor used for Hindu ceremonies is also sold at Indian grocery stores, but it is not suitable for cooking. The only type that should be used for food is that labeled as "Edible Camphor."

Religious ceremonies

In Hindu worship ceremonies (poojas), camphor is burned in a ceremonial spoon for performing aarti. It is used in the Mahashivratri celebrations of Shiva, the Hindu god of destruction and re-creation. As a natural pitch substance, it burns cool without leaving an ash residue, which symbolizes consciousness.

Toxicity

In larger quantities, it is poisonous when ingested and can cause seizures, confusion, irritability, and neuromuscular hyperactivity. In 1980, the United States Food and Drug Administration set a limit of 11 percent allowable camphor in consumer products and totally banned products labeled as camphorated oil, camphor oil, camphor liniment, and camphorated liniment (but "white camphor essential oil" contains no significant amount of camphor). Since alternative treatments exist, medicinal use of camphor is discouraged by the FDA, except for skin-related uses, such as medicated powders, which contain only small amounts of camphor. Lethal, orally ingested doses in adults are in the range 50–500 milligrams per kilogram (mg/kg) of body weight. Generally, two grams (g) causes serious toxicity and four grams is potentially lethal.

See also

Notes

  1. Maryadele J. O'Neil (ed.), The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals, 14th ed. (Whitehouse Station, NJ: Merck, ISBN 978-0911910001).
  2. David R. Lide (ed.), CRC Handbook of Chemistry and Physics, 88th ed.(Boca Raton, FL: CRC, 2007, ISBN 978-0849304880).
  3. J. Mann, et al., Natural Products: Their Chemistry and Biological Significance (Harlow, Essex, UK: Longman Scientific & Technical, ISBN 0582060095), 309-311.
  4. Camphor Online Etymology Dictionary. Retrieved June 11, 2008.
  5. Keeping rust off your tools Retrieved June 11, 2008.
  6. Mukul Kumar and Yoshinori Ando, Carbon Nanotubes from Camphor: An Environment-Friendly Nanotechnology, Journal of Physics Conference Series, (2007) 61: 643–646.
  7. Summaries of Product Characteristics (SPC) for Human medicinal products National Agency for Medicines (Finnish).

References
ISBN links support NWE through referral fees

  • Lide, David R. (ed.). 2007. CRC Handbook of Chemistry and Physics, 88th ed. Boca Raton, FL: CRC. ISBN 978-0849304880
  • Mann, J., et al. 1994. Natural Products: Their Chemistry and Biological Significance. Harlow, Essex, UK: Longman Scientific & Technical. ISBN 0582060095
  • O'Neil, Maryadele J. (ed.). 2006. The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals, 14th ed. Whitehouse Station, NJ: Merck. ISBN 978-0911910001
  • Sell, Charles. 2003. A Fragrant Introduction to Terpenoid Chemistry. Cambridge: Royal Society of Chemistry. ISBN 978-0854046812
  • Smith, Michael, and Jerry March. 2001. March's Advanced Organic Chemistry: Reactions, Mechanisms, and Structure, 5th ed. New York: Wiley. ISBN 978-0471585893

External links

All links retrieved November 25, 2023.

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