Adverts

Open Access Articles- Top Results for Butylated hydroxytoluene

Butylated hydroxytoluene

Template:Chembox UNII
Butylated hydroxytoluene
Skeletal formula of butylated hydroxytoluene
Ball-and-stick model of the butylated hydroxytoluene molecule
colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. Names

#REDIRECTmw:Help:Magic words#Other
This page is a soft redirect.-

IUPAC name
2,6-Bis(1,1-dimethylethyl)-4-methylphenol
Other names
2,6-Di-tert-butyl-4-methylphenol
2,6-Di-tert-butyl-p-cresol (DBPC)
3,5-Di-tert-butyl-4-hydroxytoluene
BHT
E321
AO-29
Avox BHT
Additin RC 7110
Dibutylated hydroxytoluene
4-Methyl-2,6-di-tert-butyl phenol
colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. Identifiers#REDIRECTmw:Help:Magic words#Other
This page is a soft redirect.-



128-37-0 7pxY
ChEBI CHEBI:34247 7pxY
ChEMBL ChEMBL146 7pxY
ChemSpider 13835296 7pxY
EC number 204-881-4
Jmol-3D images Image
KEGG D02413 7pxY
RTECS number GO7875000
colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. Properties

#REDIRECTmw:Help:Magic words#Other
This page is a soft redirect.-

C15H24O
Molar mass Lua error in Module:Math at line 495: attempt to index field 'ParserFunctions' (a nil value). g·mol−1
Appearance White to yellow powder
Odor slight, phenolic
Density 1.048 g/cm3
Melting point Script error: No such module "convert". [3]
Boiling point Script error: No such module "convert". [3]
1.1 mg/L (20 °C)[1]
Vapor pressure 0.01 mmHg (20°C)[2]
colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. Hazards

#REDIRECTmw:Help:Magic words#Other
This page is a soft redirect.-

SDS External MSDS
Main hazards Flammable
R-phrases R22-R36-R37-R38
S-phrases S26-S36
NFPA 704

Error: Must specify an image in the first line.

1
2
0
Flash point Script error: No such module "convert". [3]
US health exposure limits (NIOSH):

#REDIRECTmw:Help:Magic words#Other
This page is a soft redirect.-

#REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. style="padding-left:0.5em;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect.

#REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. none[2] #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect.-

#REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. style="padding-left:0.5em;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect.

#REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. TWA 10 mg/m3[2] #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect.-

#REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. style="padding-left:0.5em;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect.

#REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. N.D.[2] #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect.-

colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. Related compounds

#REDIRECTmw:Help:Magic words#Other
This page is a soft redirect.-


Related compounds
Butylated hydroxyanisole
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
 14pxY verify (what is10pxY/10pxN?)
Infobox references

Butylated hydroxytoluene (BHT), also known as butylhydroxytoluene, is a lipophilic organic compound, chemically a derivative of phenol, that is useful for its antioxidant properties. European and U.S. regulations allow small amounts to be used as a food additive. In addition to this use, BHT is widely used to prevent oxidation in fluids (e.g. fuel, oil) and other materials where free radicals must be controlled.

Occurrence

Phytoplankton, including the green algae Botryococcus braunii, as well as three different cyanobacteria (Cylindrospermopsis raciborskii, Microcystis aeruginosa and Oscillatoria sp.) are capable of producing BHT. Confirmation was made via gas chromatography–mass spectrometry analysis.[4]

Production

Industrially, BHT is prepared by the reaction of p-cresol (4-methylphenol) with isobutylene (2-methylpropene) catalyzed by sulfuric acid: [5]

CH3(C6H4)OH + 2 CH2=C(CH3)2 → ((CH3)3C)2CH3C6H2OH

Alternatively, BHT is prepared from 2,6-di-tert-butylphenol by hydroxymethylation or aminomethylation followed by hydrogenolysis.

Applications

Food additive

BHT is primarily used as a food additive that exploits its antioxidant properties. In the United States, it is classified as generally recognized as safe (GRAS).[6] It is approved for use in European Union under E321 and in the U.S. by the Food and Drug Administration via regulation: For example, 21 CFR §137.350(a)(4) allows BHT up to 0.0033% by weight in "enriched rice", while 9 CFR §381.147(f)(1) allows up to 0.01% in poultry "by fat content". Some food companies have voluntarily eliminated this additive from their products, and since the 1970s, it has been steadily replaced with BHA.

Antioxidant

BHT is also used as an antioxidant additive in such diverse products as cosmetics, pharmaceuticals, rubber, electrical transformer oil (at 0.35%),[7] and embalming fluid. In the petroleum industry, where BHT is known as the fuel additive AO-29, it also finds uses in hydraulic fluids, turbine and gear oils, and jet fuels,[8] among other applications. BHT is also used to prevent peroxide formation in diethyl ether and other laboratory chemicals.[9]

Some additive products contain BHT as their primary ingredient, while others contain the chemical merely as a component of their formulation, sometimes alongside butylated hydroxyanisole (BHA).

Reactions

The species behaves as a synthetic analog of vitamin E, primarily acting as a terminating agent that suppresses autoxidation, a process whereby unsaturated (usually) organic compounds are attacked by atmospheric oxygen. BHT stops this autocatalytic reaction by converting peroxy radicals to hydroperoxides. It effects this function by donating a hydrogen atom:

RO2. + ArOH → ROOH + ArO.
RO2. + ArO. → nonradical products

where R is alkyl or aryl, and where ArOH is BHT or related phenolic antioxidants. Each BHT consumes two peroxy radicals.[10]

Research

Debate surrounds the link of BHT to cancer risk, asthma and behavioral issues in children;[11] some studies show a potential to increase and some showing a decreased risk.[12][13][14] The National Toxicology Program has determined that it is noncarcinogenic in a mouse model.[6]

BHT is marketed as a health food supplement in capsule form. It has been reported to have anti-viral effects, particularly in use against herpes family viruses, sometimes in combination with L-lysine and vitamin C.[15][16][17][18][19][20][21] This latter use has made it into some of the more popular literature.[22][23][24]

Closely related phenol antioxidants exhibit low toxicity. For example, the LD50 of 2,6-di-tert-butylphenol is greater than 9 g/kg.[5]

See also

References

  1. ^ KEMI - Swedish Chemicals Agency - read the 1'st of Marts 2010 on
  2. ^ a b c d "NIOSH Pocket Guide to Chemical Hazards #0246". National Institute for Occupational Safety and Health (NIOSH). 
  3. ^ a b c BUTYLATED HYDROXYTOLUENE (ICSC)
  4. ^ Babu B, Wu JT (December 2008). "Production of Natural Butylated Hydroxytoluene as an Antioxidant by Freshwater Phytoplankton" (PDF). Journal of Phycology 44 (6): 1447–1454. doi:10.1111/j.1529-8817.2008.00596.x. 
  5. ^ a b Helmut Fiege, Heinz-Werner Voges, Toshikazu Hamamoto, Sumio Umemura, Tadao Iwata, Hisaya Miki, Yasuhiro Fujita, Hans-Josef Buysch, Dorothea Garbe, Wilfried Paulus "Phenol Derivatives" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2002. doi:10.1002/14356007.a19_313 Article Online Posting Date: June 15, 2000.
  6. ^ a b Bioassay of Butylated Hydroxytoluene (BHT) for Possible Carcinogenicity, National Toxicology Program, National Institutes of Health
  7. ^ Ficha de Datos de Seguridad, Transformador 64, page 1, retrieved December 29, 2008, (español).
  8. ^ Michael Ash, Irene Ash, Handbook of Preservatives, Synapse Information Resources, 2004. ISBN 1-890595-66-7.
  9. ^ "Diethyl ether, contains 1 ppm BHT as inhibitor, anhydrous, ≥99.7%". Sigma Aldrich. Retrieved 11 September 2012. 
  10. ^ Burton, G. W.; Ingold, K. U., "Autoxidation of biological molecules. 1. Antioxidant activity of vitamin E and related chain-breaking phenolic antioxidants in vitro", Journal of the American Chemical Society, 1981, volume 103, pp 6472 - 6477. doi:10.1021/ja00411a035
  11. ^ "Butylated hydroxytoluene (BHT)", IARC Monographs on the Evaluation of Carcinogenic Risks to Humans, 1986;40:161-206.
  12. ^ Kensler TW, Egner PA, Trush MA, Bueding E, Groopman JD, "Modification of aflatoxin B1 binding to DNA in vivo in rats fed phenolic antioxidants, ethoxyquin and a dithiothione", Carcinogenesis, 1985;6(5):759-63.
  13. ^ Williams GM, Iatropoulos MJ, "Inhibition of the hepatocarcinogenicity of aflatoxin B1 in rats by low levels of the phenolic antioxidants butylated hydroxyanisole and butylated hydroxytoluene", Cancer Lett. 1996;104(1):49-53.
  14. ^ Franklin RA, "Butylated hydroxytoluene in sarcoma-prone dogs", Lancet. 1976;1(7972):1296.
  15. ^ Snipes W, Person S, Keith A, Cupp J, "Butylated hydroxytoluene inactivates lipid-containing viruses", Science. 1975;188(4183):64-6.
  16. ^ Brugh M Jr, "Butylated hydroxytoluene protects chickens exposed to Newcastle disease virus. Science", 1977;197(4310):1291-2.
  17. ^ Richards JT, Katz ME, Kern ER, "Topical butylated hydroxytoluene treatment of genital herpes simplex virus infections of guinea pigs", Antiviral Res. 1985;5(5):281-90.
  18. ^ Kim KS, Moon HM, Sapienza V, Carp RI, Pullarkat R, "Inactivation of cytomegalovirus and Semliki Forest virus by butylated hydroxytoluene", J Infect Dis. 1978;138(1):91-4.
  19. ^ Pirtle EC, Sacks JM, Nachman RJ, "Antiviral effectiveness of butylated hydroxytoluene against pseudorabies (Aujeszky’s disease) virus in cell culture, mice, and swine", Am J Vet Res. 1986;47(9):1892-5.
  20. ^ Chetverikova LK, Ki’ldivatov II, Inozemtseva LI, Kramskaia TA, Filippov VK, et al. "Factors of antiviral resistance in the pathogenesis of influenza in mice", Vestn Akad Med Nauk SSSR. 1989;(11):63-8. [in Russian]
  21. ^ Chetverikova LK, Inozemtseva LI, "Role of lipid peroxidation in the pathogenesis of influenza and search for antiviral protective agents" Vestn Ross Akad Med Nauk. 1996;(3):37-40. [in Russian]
  22. ^ Pearson D, Shaw S, "Life Extension: A Practical Scientific Approach", New York, NY: Warner Books, Inc.; 1982:206-207.
  23. ^ Mann JA, Fowkes SW, "Wipe Out Herpes with BHT", Manhattan Beach, Calif: MegaHealth Society; 1983.
  24. ^ Fowkes SW, "The BHT Book", 2010, a free PDF e-publication, downloadable from Project Wellbeing (/steve page).

External links