4-Aminobenzoic acid

4-Aminobenzoic acid (also known as para-aminobenzoic acid or PABA because the number 4 carbon in the benzene ring is also known as the para position) is an organic compound with the formula H2NC6H4CO2H. PABA is a white solid, although commercial samples can appear gray. It is slightly soluble in water. It consists of a benzene ring substituted with amino and carboxyl groups. The compound occurs extensively in the natural world.

4-Aminobenzoic acid
Skeletal formula of PABA
C=black, H=white, O=red, N=blue
Names
Preferred IUPAC name
4-Aminobenzoic acid
Other names
para-Aminobenzoic acid
p-Aminobenzoic acid
PABA
Vitamin B10
Vitamin Bx
Bacterial vitamin H1
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.005.231
KEGG
UNII
Properties
C7H7NO2
Molar mass 137.138 g·mol−1
Appearance White-grey crystals
Density 1.374 g/mL
Melting point 187 to 189 °C (369 to 372 °F; 460 to 462 K)
Boiling point 340 °C (644 °F; 613 K)
1 g/170 mL (25 °C)
1 g/90 mL (90 °C)
Acidity (pKa)
  • 2.50 (carboxyl; H2O)
  • 4.87 (amino; H2O)[1]
Hazards
Main hazards eye irritant, some persons may be allergic to this compound
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)
Infobox references

Production and occurrence

In industry, PABA is prepared mainly by two routes:

Food sources of PABA include liver, brewer's yeast (and unfiltered beer), kidney, molasses, mushrooms, and whole grains.[3]

A review on this compound.[4]

Biology

Biochemistry
Tetrahydrofolate synthesis pathway

PABA is an intermediate in the synthesis of folate by bacteria, plants, and fungi.[5] Many bacteria, including those found in the human intestinal tract such as E. coli, generate PABA from chorismate by the combined action of the enzymes 4-amino-4-deoxychorismate synthase and 4-amino-4-deoxychorismate lyase.[6] Plants produce PABA in their chloroplasts, and store it as a glucose ester (pABA-Glc) in their tissues. Humans lack the enzymes to convert PABA to folate, so require folate from dietary sources such as green leafy vegetables. In humans, PABA is considered nonessential and, although it has been referred to historically as "vitamin Bx", is no longer recognized as a vitamin,[5] because most people have a microbiome that will generate PABA.

Sulfonamide drugs are structurally similar to PABA, and their antibacterial activity is due to their ability to interfere with the conversion of PABA to folate by the enzyme dihydropteroate synthetase. Thus, bacterial growth is limited through folate deficiency.[7]

Medical use

The potassium salt is used as a drug against fibrotic skin disorders, such as Peyronie's disease, under the trade name Potaba.[8] PABA is also occasionally used in pill form by sufferers of irritable bowel syndrome to treat its associated gastrointestinal symptoms, and in nutritional epidemiological studies to assess the completeness of 24-hour urine collection for the determination of urinary sodium, potassium, or nitrogen levels.

Nutritional supplement

Despite the lack of any recognized syndromes of PABA deficiency in humans, except for those who lack the colonic bacteria that generate PABA, many claims of benefit are made by commercial suppliers of PABA as a nutritional supplement. The benefit is claimed for fatigue, irritability, depression, weeping eczema (moist eczema), scleroderma (premature hardening of the skin), patchy pigment loss in the skin (vitiligo), and premature grey hair.[9]

Commercial and industrial use

PABA finds use mainly in the biomedical sector. Other uses include its conversion to specialty azo dyes and crosslinking agents. PABA is also used as a biodegradable pesticide, though its use is now limited due to evolution of new variants of bio-pesticides.

In the past, PABA was widely used in sunscreens as a UV filter. It is a UVB absorber, meaning it can absorb wavelengths between 290 and 320 nm.[10] while still allowing UVA wavelengths between 320-400 nm to pass through, producing a tan.[11] Patented in 1943, PABA was one of the first active ingredients to be used in sunscreen.[12] The first in vivo studies on mice showed that PABA reduced UV damage. In addition, it was shown to protect against skin tumors in rodents.[13] Animal and in vitro studies in the early 1980s suggested PABA might increase the risk of cellular UV damage.[14] On the basis of these studies, as well as problems with allergies and clothing discoloration, PABA fell out of favor as a sunscreen. However, water-insoluble PABA derivatives such as padimate O are currently used in some cosmetic products including mascara, concealer, and matte lipsticks. [15]


As of 2008, the advancement of new sunscreen is focused on developing a broad spectrum of active ingredients that provide consistent protection across all wavelengths, including UVA. Researchers are considering the PABA–TiO2 Hybrid Nanostructures that result from the method of aqueous in situ synthesis with PABA and TiO2.[16]

Safety considerations

PABA is largely nontoxic; the median lethal dose of PABA in dogs (oral) is 2 g/kg.[2] Allergic reactions to PABA can occur. It is formed in the metabolism of certain ester local anesthetics, and many allergic reactions to local anesthetics are the result of reactions to PABA.[17]

See also

References
  1. Haynes, William M., ed. (2016). CRC Handbook of Chemistry and Physics (97th ed.). CRC Press. p. 5–89. ISBN 978-1498754286.
  2. Maki, T.; Takeda, K. (2000). "Benzoic Acid and Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Wiley-VCH. doi:10.1002/14356007.a03_555. ISBN 3527306730.
  3. "Nutritional Health Resource". Archived from the original on 2009-12-16. Retrieved 2009-11-21.
  4. Kluczyk, Alicja; Popek, Tomasz; Kiyota, Taira; de Macedo, Pierre; Stefanowicz, Piotr; Lazar, Carmen; Konishi, Yasuo (2002). "Drug Evolution: p-Aminobenzoic Acid as a Building Block". Current Medicinal Chemistry. 9 (21): 1871–1892. doi:10.2174/0929867023368872. ISSN 0929-8673. PMID 12369873.
  5. "Para-aminobenzoic acid". Medline Plus Medical Encyclopedia. United States National Institutes of Health. Retrieved 24 January 2014.
  6. Folate Synthesis (Abstract)
  7. Brown GM (1962). "The biosynthesis of folic acid. II. Inhibition by sulfonamides". J. Biol. Chem. 237 (2): 536–40. doi:10.1016/S0021-9258(18)93957-8. PMID 13873645.
  8. "Compound Summary on PubChem". PubChem. National Institute of Health: National Library of Medicine. 2006. Retrieved 2006-04-05.
  9. "Health Library (Supplements) PABA". Archived from the original on 2017-08-04. Retrieved 2017-08-04.
  10. Melanoma Madness The scientific flap over sunscreens and skin cancer -- Chemical studies, Science News Online, 6/6/98 (accessed 10/1/2009, 2009)
  11. Rahal, R.; Daniele, S.; Hubert-Pfalzgraf, L. G.; Guyot-Ferréol, V.; Tranchant, J (2008). "Synthesis of para-Amino Benzoic Acid–TiO2 Hybrid Nanostructures of Controlled Functionality by an Aqueous One-Step Process". European Journal of Inorganic Chemistry. 2008 (6): 980–987. doi:10.1002/ejic.200700971.CS1 maint: uses authors parameter (link)
  12. F. P.; Mitchnick, M.; Nash, J. F. A Review of Sunscreen Safety and Efficacy Photochem. Photobiol. 1998, 68, 243 <last_page> 256.
  13. H.; Thune, P.; Eeg Larsen, T. The inhibiting effect of PABA on photocarcinogenesis Arch. Dermatol. Res. 1990, 282, 38 <last_page> 41
  14. Osgood, Pauline J.; Moss, Stephen H.; Davies, David J. G. (1982). "The Sensitization of Near-Ultraviolet Radiation Killing of Mammalian Cells by the Sunscreen Agent Para-aminobenzoic Acid". Journal of Investigative Dermatology. 79 (6): 354–7. doi:10.1111/1523-1747.ep12529409. PMID 6982950.
  15. , "Matte cosmetic compositions"
  16. Rahal, R.; Daniele, S.; Hubert-Pfalzgraf, L. G.; Guyot-Ferréol, V.; Tranchant, J (2008). "Synthesis of para-Amino Benzoic Acid–TiO2 Hybrid Nanostructures of Controlled Functionality by an Aqueous One-Step Process". European Journal of Inorganic Chemistry. 2008 (6): 980–987. doi:10.1002/ejic.200700971.CS1 maint: uses authors parameter (link)
  17. Toxicity, Local Anesthetics: eMedicine Emergency Medicine
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.