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691941

Sigma-Aldrich

3-Benzyladenine

95%

Synonym(s):

3-Benzyl-3H-purin-6-amine

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About This Item

Empirical Formula (Hill Notation):
C12H11N5
CAS Number:
7280-81-1
Molecular Weight:
225.25
MDL number:
MFCD02167626
UNSPSC Code:
12352100
PubChem Substance ID:
329761451
NACRES:
NA.22

Quality Level

100

Assay

95%

form

solid

mp

268-275 °C

SMILES string

Nc1ncn(Cc2ccccc2)c3ncnc13

InChI

1S/C12H11N5/c13-11-10-12(15-7-14-10)17(8-16-11)6-9-4-2-1-3-5-9/h1-5,7-8H,6,13H2

InChI key

ZRRXJVVXTVXDII-UHFFFAOYSA-N

Related Categories

Pictograms

Exclamation markHealth hazard
GHS07,GHS08

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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C J Li et al.
Shi yan sheng wu xue bao, 27(4), 457-462 (1994-12-01)
The effect of purine on the meiosis of mouse oocytes was studied. When adenine and benzyladenine, a similar substance of adenine, was microinjected into the germinal vesicle of oocytes, the meiotic maturation of oocytes could be obviously arrested depending on
Yuki Ishii et al.
Biochimica et biophysica acta, 1643(1-3), 11-24 (2003-12-05)
Cytokinins are important purine derivatives that act as hormones to control many processes in plants. Cytokinins such as isopentenyladenine (IPA), kinetin and benzyladenine were very effective at inducing the granulocytic differentiation of human myeloid leukemia HL-60 cells. The metabolism of
V Prevost et al.
Carcinogenesis, 14(2), 199-204 (1993-02-01)
Immunoaffinity gels were prepared by coupling monoclonal antibody (Mab) EM-6-47 to protein A-Sepharose, and were used to make small columns retaining 3-alkyladenines (3-alkAde) of diverse structure. An analytical procedure for determination of 3-methyladenine (3-MeAde), 3-ethyladenine (3-EtAde), 3-(2-hydroxyethyl)adenine (3-HOEtAde) and 3-benzyladenine
H Yamada et al.
Plant & cell physiology, 42(9), 1017-1023 (2001-09-29)
Common histidine-to-aspartate (His-->Asp) phosphorelay is a paradigm of signal transduction in both prokaryotes and eukaryotes for the propagation of certain environmental stimuli, in which histidine (His)-kinases play central roles as sensors for environmental signals. For the higher plant, Arabidopsis thaliana

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