Name | N-benzyl-9-(2-tetrahydropyranyl)adenine plant cel |
Synonyms | BPA PBA Pyranyl Benzyladenine PYRANYL BENZYLADENINE Pyranyl Benzyl Adenine N-BENZYL-9-(2'-TETRAHYDROPYRANYL)ADENINE 9-(oxan-2-yl)-N-(phenylmethyl)purin-6-amine n-benzyl-9-(tetrahydro-2h-pyran-2-yl)adenine N-Benzyl-9-(tetrahydro-2H-pyran-2-yl)adenine N6-BENZYL-9-(2-TETRAHYDROPYRANYL)ADENINE (BPA) benzyl-(9-tetrahydropyran-2-ylpurin-6-yl)amine N-benzyl-9-(2-tetrahydropyranyl)adenine plant cel 2-(phenylmethyl)-8-(2H-pyran-2-yl)-7H-purin-6-amine N-benzyl-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine N-(Phenylmethyl)-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine |
CAS | 2312-73-4 |
InChI | InChI=1/C17H19N5O/c1-2-6-13(7-3-1)10-18-16-15-17(20-11-19-16)22(12-21-15)14-8-4-5-9-23-14/h1-3,6-7,11-12,14H,4-5,8-10H2,(H,18,19,20) |
Molecular Formula | C17H19N5O |
Molar Mass | 309.37 |
Density | 1.0874 (rough estimate) |
Melting Point | 108-110 °C |
Boling Point | 449.64°C (rough estimate) |
Flash Point | 281.1°C |
Vapor Presure | 8.96E-12mmHg at 25°C |
pKa | 3.51±0.10(Predicted) |
Storage Condition | −20°C |
Refractive Index | 1.7500 (estimate) |
In vitro study | The cytokinin derivative BAP9THP is an important component of these protocols: culture of isolated apical meristem or growing shoot apices on media containing this compound resulted in signifcant shoot multiplication. both BAP9THP and BAP9THF are found to delay senescence and induce several growth responses more strongly than BAP. |
Hazard Symbols | Xn - Harmful |
Risk Codes | 22 - Harmful if swallowed |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. |
WGK Germany | 3 |
RTECS | UO7510000 |
Toxicity | LD50 orl-rat: 1640 mg/kg 85AREA 3,48,76/77 |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
biological activity | BAP9THP is a synthetic cytokinin derivative and growth regulator. The promoting effect of BAP9THP on chlorophyll retention (and delayed senescence) in plant tissues was unusually strong, while the growth of tobacco callus was almost as strong as that of 6-benzylaminopurine (BAP). The induction effect of BAP9THP on adventitious buds was significantly stronger than that of N6-isopentenyladenine or Kinetin. |
use | is a commonly used growth regulator for flowers. it has the effects of inducing callus differentiation and germination, promoting fruit setting of some fruit trees and delaying chlorophyll degradation |
category | pesticide |
toxicity classification | poisoning |
acute toxicity | oral-rat LD50: 1640 mg/kg |
flammability hazard characteristics | combustible; combustion produces toxic nitrogen oxide smoke |
storage and transportation characteristics | ventilation and low temperature drying |
fire extinguishing agent | dry powder, foam, sand, carbon dioxide, mist water |