6-Benzylaminopurine - 10mM in DMSO , CAS No.1214-39-7

CAS: 1214-39-7 Cat. No.: B420930 Molecular Weight: 225.25 Beilstein Registry Number: 19406 EC Number: 214-927-5
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GRADE & PURITY 10mM in DMSO
Synonyms
6-Benzylaminopurine|1214-39-7|Benzyladenine|N6-Benzyladenine|6-Benzyladenine|N-Benzyladenine|N-Benzyl-9H-purin-6-amine|6-(Benzylamino)purine|Benzylaminopurine|Cytokinin B|6-BAP|Adenine, N-benzyl-|N-benzyl-7H-purin-6-amine|N(6)-Benzylaminopurine|Benzyl(pur
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
Status
Price
Qty
1ml
B420930-1ml
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 17 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

6-Benzylaminopurine is a plant growth regulator that belongs to the class of first generation synthetic cytokinin used in agriculture.

Specifications

Synonyms
6-Benzylaminopurine | 1214-39-7 | Benzyladenine | N6-Benzyladenine | 6-Benzyladenine | N-Benzyladenine | N-Benzyl-9H-purin-6-amine | 6-(Benzylamino)purine | Benzylaminopurine | Cytokinin B | 6-BAP | Adenine, N-benzyl- | N-benzyl-7H-purin-6-amine | N(6)-Benzylaminopurine | Benzyl(pur
Specifications & Purity
10mM in DMSO
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
Store at -80°C
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers
Canonical SmilesC1=CC=C(C=C1)CNC2=NC=NC3=C2NC=N3
IUPAC NameN-benzyl-7H-purin-6-amine
InChIKeyNWBJYWHLCVSVIJ-UHFFFAOYSA-N
INCHI1S/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)
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=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

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✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassImidazopyrimidines
SubclassPurines and purine derivatives
Intermediate Tree Nodes 6-aminopurines
Direct Parent6-alkylaminopurines
Alternative Parents Benzylamines  Secondary alkylarylamines  Aminopyrimidines and derivatives  Imidolactams  Imidazoles  Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic 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
DescriptionThis 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
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CDK2 Tchem Cyclin-dependent kinase 2 (9050 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CDK1 Tchem Cyclin-dependent kinase 1 (3927 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HL-60 (67320 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RD (1212 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BRD4 Tchem Bromodomain-containing protein 4 (13122 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
LMNA Tbio Prelamin-A/C (36751 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PI4K2A Tbio Phosphatidylinositol 4-kinase, PI4K (160 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NT5C2 Tbio Cytosolic purine 5'-nucleotidase (72 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Mapk1 MAP kinase ERK2 (650 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nicotiana tabacum (382 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Saccharomyces cerevisiae (19171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Enterovirus A71 (1246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
J774.A1 (2436 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CKX1 Cytokinin dehydrogenase 1 (36 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bacillus anthracis (2936 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Phytophthora citrophthora (55 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FTL Ferritin light chain (43324 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Tick-borne encephalitis virus (132 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
Melt Point(°C)230-233°C
Molecular Weight225.250 g/mol
XLogP32.100
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count3
Exact Mass225.101 Da
Monoisotopic Mass225.101 Da
Topological Polar Surface Area66.500 Ų
Heavy Atom Count17
Formal Charge0
Complexity241.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Documents & Articles
Citations of This Product
References
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).  [PMID:] [10.1007/s11627-022-10292-7]
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,      [PMID:] [10.1021/acssuschemeng.2c03184]
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).  [PMID:] [10.1007/s11627-020-10133-5]
4. Yehong Han, Zhiqiang Wang, Jun Jia, Ligai Bai, Haiyan Liu, Shigang Shen, Hongyuan Yan.  (2019)  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,      [PMID:31864185] [10.1016/j.foodchem.2019.125999]
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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).  [PMID:] [10.1007/s12161-018-1168-3]
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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).  [PMID:] [10.3390/horticulturae10060587]
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,      [PMID:38478706] [10.1021/acs.jafc.4c00309]
11. Huifeng Deng, Yanqun Yang, Jianbin Ju, Yu Jiang, Xiaowen Huang, Zhenyu Li, Rui Shi, Guihua Ruan, Yipeng Huang.  (2024)  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,      [PMID:39580982] [10.1016/j.chroma.2024.465540]
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,      [PMID:] [10.1016/j.microc.2024.110873]
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