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6-Benzylaminopurine - for plant cell culture,≥99.0%, high purity , CAS No.1214-39-7
Basic Description
Synonyms
CBDivE_001815 | HMS1667I06 | HY-B0941 | STK858495 | BPBio1_000129 | HMS2095F19 | KXG6A989PS | EINECS 214-927-5 | N(sup 6)-Benzyladenine | N(Sup 6)-benzyl-Adenine | Benzyl(purin-6-yl)amine | BSPBio_000117 | BA (Growth stimulant) | GEO-00296 | N-(Phenylmeth
Specifications & Purity
for plant cell culture, ≥99%
Biochemical and Physiological Mechanisms
Plant cell division factor. Widely used synthetic cytokinin supplement for plant growth media. Stimulates Ca 2+ influx (K M = 1 nM) by moss protoplasts. Induces positive inotropic effects through activation of P2X and P2Y (P2-purinergic receptors) in rat
Storage Temp
Desiccated
Shipped In
Normal
Grade
for plant cell culture
Note
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description
6-Benzylaminopurine is a plant growth regulator that belongs to the class of first generation synthetic cytokinin used in agriculture.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Imidazopyrimidines
Subclass
Purines and purine derivatives
Intermediate Tree Nodes
6-aminopurines
Direct Parent
6-alkylaminopurines
Alternative Parents
Benzylamines Secondary alkylarylamines Aminopyrimidines and derivatives Imidolactams Imidazoles Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
6-alkylaminopurine - Benzylamine - Aminopyrimidine - Secondary aliphatic/aromatic amine - Monocyclic benzene moiety - Pyrimidine - Benzenoid - Imidolactam - Imidazole - Heteroaromatic compound - Azole - Secondary amine - Azacycle - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organopnictogen compound - Amine - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 6-alkylaminopurines. These are compounds that contain an alkylamine group attached at the 6-position of a purine. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring.
External Descriptors
a small molecule
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Associated Targets(non-human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
Pubchem Sid
488183573
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488183573
IUPAC Name
N-benzyl-7H-purin-6-amine
INCHI
InChI=1S/C12H11N5/c1-2-4-9(5-3-1)6-13-11-10-12(15-7-14-10)17-8-16-11/h1-5,7-8H,6H2,(H2,13,14,15,16,17)
InChIKey
NWBJYWHLCVSVIJ-UHFFFAOYSA-N
Smiles
C1=CC=C(C=C1)CNC2=NC=NC3=C2NC=N3
Isomeric SMILES
C1=CC=C(C=C1)CNC2=NC=NC3=C2NC=N3
WGK Germany
2
RTECS
AU6252200
Packing Group
III
Molecular Weight
225.25
Beilstein
19406
Reaxy-Rn
19406
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=19406&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
Soluble in water, methanol and acetone. Slightly soluble in ethyl acetate and dichloromethane and toluene. Insoluble in n-hexane.
Melt Point(°C)
230-233°C
Molecular Weight
225.250 g/mol
XLogP3
2.100
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
3
Exact Mass
225.101 Da
Monoisotopic Mass
225.101 Da
Topological Polar Surface Area
66.500 Ų
Heavy Atom Count
17
Formal Charge
0
Complexity
241.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
Citations of This Product
1.
Xiao Xu, Zhang Chunling, Liu Yang, Wang Xiaofei, You Chunxiang.
(2023)
Functional identification of apple Baby Boom in genetic transformation and somatic embryogenesis. IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-PLANT,
59
(1):
(1-13).
2.
Yuzhang Yang, Yunqian Gong, Xingliang Li, Minji Li, Qinping Wei, Beibei Zhou, Junke Zhang.
(2022)
Alkaline-Stable Peroxidase Mimics Based on Biological Metal–Organic Frameworks for Recyclable Scavenging of Hydrogen Peroxide and Detecting Glucose in Apple Fruits. ACS Sustainable Chemistry & Engineering,
10
(32):
(10685–10698).
3.
Li Xiuyu, Zhang Zijie, Ren Yunhui, Feng Yue, Guo Qi, Dong Li, Sun Yuhan, Li Yun.
(2021)
Induction and early identification of tetraploid black locust by hypocotyl in vitro. IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-PLANT,
57
(3):
(372-379).
4.
Yehong Han, Zhiqiang Wang, Jun Jia, Ligai Bai, Haiyan Liu, Shigang Shen, Hongyuan Yan.
(2020)
Newly designed molecularly imprinted 3-aminophenol-glyoxal-urea resin as hydrophilic solid-phase extraction sorbent for specific simultaneous determination of three plant growth regulators in green bell peppers. FOOD CHEMISTRY,
311
(125999).
5.
Mingwei Wang, Hailiang Nie, Dandan Han, Xiaoqiang Qiao, Hongyuan Yan, Shigang Shen.
(2019)
Cauliflower-like resin microspheres with tuneable surface roughness as solid-phase extraction adsorbent for efficient extraction and determination of plant growth regulators in cucumbers. FOOD CHEMISTRY,
295
(259).
6.
Yunlei Zhou, Huanshun Yin, Yue Wang, Chengji Sui, Minghui Wang, Shiyun Ai.
(2018)
Electrochemical aptasensors for zeatin detection based on MoS2 nanosheets and enzymatic signal amplification. ANALYST,
143
(21):
(5185-5190).
7.
Wang Mingwei, Zhang Hua, Jia Jun, Han Dandan, Han Yehong, Yan Hongyuan.
(2018)
An Extraction Method for Determination of 6-Benzyladenine in Bean Sprout by Graphene Oxide/Polypyrrole Composite Adsorbent. Food Analytical Methods,
11
(6):
(1832-1839).
8.
Bingchen Li, Huanshun Yin, Yunlei Zhou, Minghui Wang, Jun Wang, Shiyun Ai.
(2018)
Photoelectrochemical detection of miRNA-319a in rice leaf responding to phytohormones treatment based on CuO-CuWO4 and rolling circle amplification. SENSORS AND ACTUATORS B-CHEMICAL,
255
(1744).
9.
Jiangmei Hu, Junhuo Cai, Xinrui Hu, Lijun Wang, Qiangqiang Cheng, Xiuhua Tao.
(2024)
Efficient In Vitro Propagation of Turpinia arguta and Quantitative Analysis of Its Ligustroflavone and Rhoifolin Content. Horticulturae,
10
(6):
(587).
10.
Yan-Xia Zhang, Yi-Da Zhang, Yan-Ping Shi.
(2024)
Novel Small Molecule Matrix Screening for Simultaneous MALDI Mass Spectrometry Imaging of Multiple Lipids and Phytohormones. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,
72
(12):
(6762-6771).
11.
Huifeng Deng, Yanqun Yang, Jianbin Ju, Yu Jiang, Xiaowen Huang, Zhenyu Li, Rui Shi, Guihua Ruan, Yipeng Huang.
(2025)
Rapid analysis of six cytokinins in tomato plants using phenylboronic acid and ionic liquid functionalized monolithic capillary column combined with UHPLC-MS/MS. JOURNAL OF CHROMATOGRAPHY A,
1739
(465540).
12.
Linfan Guo, Ganhong Zheng, Xiujuan Wang, Yupeng Yuan, Chuhong Zhu.
(2024)
Uniform monolayer of branched silver nanoplates-assembled nanoparticles for sensitive and reproducible SERS detection of harmful molecules. MICROCHEMICAL JOURNAL,
203
(110873).
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12 Citations
I2104107