6-Benzylaminopurine

6-Benzylaminopurine
Skeletal formula of 6-benzylaminopurine
Ball-and-stick model of the 6-benzylaminopurine molecule
Names
Systematic IUPAC name
N-(Phenylmethyl)-7H-purin-6-amine
Other names
Benzyl adenine; 6-Benzyladenine
Identifiers
1214-39-7 YesY
ChEBI CHEBI:29022 YesY
ChEMBL ChEMBL228862 YesY
ChemSpider 56177 YesY
Jmol interactive 3D Image
KEGG C11263 YesY
PubChem 62389
Properties
C12H11N5
Molar mass 225.26 g·mol−1
Appearance White to off-white powder
Hazards
Safety data sheet External MSDS
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

6-Benzylaminopurine, benzyl adenine or BAP is a first-generation synthetic cytokinin that elicits plant growth and development responses, setting blossoms and stimulating fruit richness by stimulating cell division. It is an inhibitor of respiratory kinase in plants, and increases post-harvest life of green vegetables. Influence of cytokinin as 6-benzylaminopurine (BAP) in combination with other methods on postharvest green color retention on broccoli heads and asparagus spears, showed positive results for quality retention. Treatment with 10 and 15 ppm BAP can be used to extend shelf life of fresh-cut broccoli florets and shredded cabbage during storage at 6±1°C at commercial level.[1][2]

6-Benzylaminopurine was first synthesized and tested in the laboratories of plant physiologist Folke K. Skoog.

See also

References

  1. Siddiqui, M. W.; Bhattacharjya, A.; Chakraborty, I. and Dhua, R. S. 2011. 6-benzylaminopurine improves shelf life, organoleptic quality, and health-promoting compounds of fresh-cut broccoli florets. Journal of Scientific and Industrial Research, 70 (6): 461–465.
  2. Siddiqui, M.W.; Bhattacharjya, A. and Chakraborty, I. 2011. Maintaining organoleptic quality of minimally processed cabbage using 6-benzylaminopurine. International Symposium on System Intensification towards Food and Security, Feb. 24- 27, 2011, Kalyani, Nadia, West Bengal, India, p. 405.


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