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3-Benzyladenine (CAS 7280-81-1)

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Alternate Names:
3-Benzyl-3H-purin-6-amine
Application:
3-Benzyladenine is a nucleic acid derivative
CAS Number:
7280-81-1
Molecular Weight:
225.25
Molecular Formula:
C12H11N5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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3-Benzyladenine (3-BA) is an extensively utilized plant growth regulator and hormone in various scientific research applications. As a naturally occurring plant hormone, it assumes a role in the regulation of plant growth and development. The versatile nature of 3-Benzyladenine has found applications in numerous plant biotechnological endeavors, including crop production and genetic engineering. Moreover, 3-Benzyladenine serves as useful for investigating the biochemical and physiological effects of plant hormones on plants. The applications of 3-Benzyladenine span a wide array of scientific research domains, encompassing crop production, genetic engineering, and plant physiology. Its utilization has proven instrumental in studying the intricate interplay between plant hormones and the growth and development of plants. Furthermore, 3-Benzyladenine has shed light on the effects of environmental stressors on plants, facilitating a deeper understanding of their resilience mechanisms. In the realm of genetic engineering, 3-Benzyladenine has provided insights into the transformative effects of manipulating plant genetics. Mechanistically, 3-Benzyladenine exerts its influence by binding to and activating specific receptors responsible for plant growth hormones. Activation of these receptors triggers a cascade of events, leading to the production of plant hormones that, in turn, impact plant growth and development. Additionally, 3-Benzyladenine exerts control over the expression of specific genes, thereby instigating changes in plant morphology and physiology.


3-Benzyladenine (CAS 7280-81-1) References

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  3. Urinary markers for measuring exposure to endogenous and exogenous alkylating agents and precursors.  |  Shuker, DE., et al. 1993. Environ Health Perspect. 99: 33-7. PMID: 8319651
  4. Immunoaffinity purification and gas chromatography-mass spectrometric quantification of 3-alkyladenines in urine: metabolism studies and basal excretion levels in man.  |  Prevost, V., et al. 1993. Carcinogenesis. 14: 199-204. PMID: 8435861
  5. N-Nitrosobenzylmethylamine is activated to a DNA benzylating agent in rats.  |  Peterson, LA. 1997. Chem Res Toxicol. 10: 19-26. PMID: 9074798
  6. Activity of Escherichia coli DNA-glycosylases on DNA damaged by methylating and ethylating agents and influence of 3-substituted adenine derivatives.  |  Tudek, B., et al. 1998. Mutat Res. 407: 169-76. PMID: 9637245
  7. Cyclobutane Formation from Mercury-Photosensitized Reactions of Ethylene  |  Chesick, J. P. 1963. Journal of the American Chemical Society. 85(22): 3718-3719.
  8. Synthesis of 3-(2'-deoxy-D-erythro-pentofuranosyl)adenine. Application of a new protecting group, pivaloyloxymethyl(Pom)  |  Rasmussen, M., & Leonard, N. J. 1967. Journal of the American Chemical Society. 89(21): 5439-5445.
  9. Specific dealkylation of 3-benzyladenines in the presence of 9-benzyladenines  |  Weinstock, L. M., Tull, R. J., Douglas, A. W., & Shinkai, I. 1980. The Journal of Organic Chemistry. 45(26): 5419-5421.
  10. Purines. LXVI. Adenine 7-Oxide: Its Synthesis, Chemical Properties, and X-ray Molecular Structure  |  FUJII, T., OGAWA, K., SAITO, T., KoBAYAsHI, K., ITAYA, T., DATE, T., & OKAMURA, K. 1995. Chemical and pharmaceutical bulletin. 43(1): 53-62.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

3-Benzyladenine, 100 mg

sc-231480
100 mg
$152.00