Description

N6-Benzyladenine (CAS 1214-39-7) is a synthetic cytokinin plant growth regulator with the molecular formula C₁₂H₁₁N₅ and IUPAC name N-benzyl-7H-purin-6-amine. This high-purity compound is widely utilized in plant tissue culture and agricultural research due to its ability to promote cell division, shoot proliferation, and delayed senescence. As a benzyl-substituted adenine derivative, it exhibits superior stability and bioactivity compared to natural cytokinins. Our N6-Benzyladenine is rigorously tested for purity (>98% by HPLC) and is supplied as a white to off-white crystalline powder with excellent solubility in dilute acids or bases. Suitable for in vitro applications, this product is ideal for researchers studying plant morphogenesis, micropropagation protocols, and hormonal regulation in plant systems. Each batch is accompanied by comprehensive analytical documentation including NMR and MS spectra for verification.

Properties

• CAS Number: 1214-39-7
• Complexity: 241
• 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)
• InChI Key: NWBJYWHLCVSVIJ-UHFFFAOYSA-N
• LogP: log Kow = 1.57
• Exact Mass: 225.10144537
• Molecular Formula: C12H11N5
• Molecular Weight: 225.25
• SMILES: C1=CC=C(C=C1)CNC2=NC=NC3=C2NC=N3
• Topological: 66.5
• Monoisotopic Mass: 225.10144537
• Physical Description: Colorless solid; Technical product is off-white solid; White solid; Formulated as soluble concentrate/liquid; [Reference #1] Light yellow powder;
• Color/Form: Colorless, fine needles
• Melting Point: 234-235 °C
• Solubility: Insoluble in most common organic solvents; Soluble in dimethylformamide, dimethyl sulfoxide
• Vapor Pressure: 2.373X10-6 mPa at 20 °C
• Synonyms: 6-Benzylaminopurine, 1214-39-7, Benzyladenine, N6-Benzyladenine, 6-Benzyladenine, N-Benzyladenine, 6-(Benzylamino)purine, Benzylaminopurine, Adenine, N-benzyl-, 6-BAP, N-benzyl-7H-purin-6-amine, N(6)-Benzylaminopurine, Benzyl(purin-6-yl)amine, 6-(N-Benzylamino)purine, 1H-PURIN-6-AMINE, N-(PHENYLMETHYL)-, Pro-Shear, BA (Growth stimulant), BAP (growth stimulant), N(sup 6)-Benzyladenine, Verdan senescence inhibitor, Caswell No. 081EE, N-Benzyl-adenine, N(sup 6)-(Benzylamino)purine, N-(Phenylmethyl)-1H-purin-6-amine, N(6)-(benzylamino)purine, Adenine, N(sup 6)-benzyl-, Adenine, N6-benzyl-, CCRIS 4351, SD 4901, SQ 4609, ABG 3034, Benzyl Aminopurine, 6-[(phenylmethyl)amino]-9H-purine, EINECS 214-927-5, KXG6A989PS, NSC 40818, n(6)-benzyladenine, CYTOPURINE, CHEBI:29022, HSDB 7667, NSC-40818, BENZYLADENINE [MI], BENZYLADENINE, 6-, 9H-Purin-6-amine, N-(phenylmethyl)-, BENZYLADENINE [HSDB], BAP 99, 6-((phenylmethyl)amino)-9H-purine, NBenzyladenine, 6benzyladenine, ProShear, Adenine, Nbenzyl, 6-benzylaminopurin, 6(Benzylamino)purine, Benzyl(purin6yl)amine, 6(NBenzylamino)purine, N(6)Benzylaminopurine, 6-BA cpd, N(sup 6)Benzyladenine, Adenine, N(sup 6)benzyl, BENZYLADENINE [INCI], N(Phenylmethyl)1Hpurin6amine, N(sup 6)(Benzylamino)purine, 1HPurin6amine, N(phenylmethyl), 9HPurin6amine, N(phenylmethyl), N-benzyladenine, monosodium salt, N-benzyladenine, monopotassium salt, USEPA/OPP Pesticide Code: 116901, N-Benzyl-9H-purin-6-amine, Cytokinin B, Aminopurine, 6-benzyl, 6-Benzyl adenine, N-6-Benzyladenine, 6-(Benzylamino)-9H-purine, MFCD00005572, benzylpurin-6-ylamine, N-benzyl-1H-purin-6-amine, MLS000532693, CHEMBL228862, DTXSID7032630, SMR000140130, CAS-1214-39-7, 6-BA, 6-(n-benzyl)aminopurine, UNII-KXG6A989PS, benzyl-(7h-purin-6-yl)-amine, BAP (cytokinin), Prestwick_414, n6-benzylaminopurine, benzylaminopurine, 6-, N-Benzyladenine, 8CI, N(Sup6)-Benzyladenine, BA (growth stimulator), Opera_ID_868, Prestwick0_000189, Prestwick1_000189, Prestwick2_000189, Prestwick3_000189, 6-Benzylaminopurine6-BAP, N(Sup 6)-benzyl-Adenine, CBKinase1_000521, CBKinase1_012921, Cambridge id 5131951, TimTec1_001722, Oprea1_747691, Oprea1_785203, Oprea1_830563, SCHEMBL35562, SCHEMBL37357, SCHEMBL37358, BSPBio_000117, CBDivE_001815, MLS001074298, SPBio_002038, 6-Benzylaminopurine, 99.0%, 6-Benzylaminopurine (Standard), BPBio1_000129, DTXCID5012630, HY-B0941R, NWBJYWHLCVSVIJ-UHFFFAOYSA-, 6-Benzylaminopurine 100 microg/mL in Acetonitrile/Acetone, HMS1538O06, HMS1568F19, HMS1667I06, HMS2095F19, HMS2234B24, HMS3374C09, HMS3712F19, 6-benzyladenine 6-benzylaminopurine, HY-B0941, MSK24051, NSC40818, STR06184, N-(phenylmethyl)-7H-purin-6-amine, Tox21_301307, AC7620, BDBM50205363, CCG-55533, GEO-00296, MFCD00051031, N-(Phenylmethyl)-9H-Purin-6-amine, s4511, STK858495, AKOS002304241, AKOS005257767, 7H-purin-6-amine, N-(phenylmethyl)-, AC-5488, CCG-220189, FB02966, KS-5285, PS-3425, 6-Benzylaminopurine, analytical standard, N-benzyl-9H-purin-6-amine, AldrichCPR, NCGC00016571-01, NCGC00016571-02, NCGC00016571-03, NCGC00016571-04, NCGC00016571-05, NCGC00255357-01, ST020598, SY014632, 6-Benzylaminopurine, >=99.0% (HPLC), B1088, NS00005241, BA; N6-Benzyladenine; N6-Benzyladenine; BA, EN300-40176, 6-Benzylaminopurine, plant cell culture tested, Q419946, SR-01000644553, 6-Benzylaminopurine, Vetec(TM) reagent grade, 98%, SR-01000644553-1, SR-01000644553-2, BA ; N6-Benzyladenine ; N6-Benzyladenine ; BA, BRD-K62929068-001-05-8, BRD-K62929068-001-15-7, BRD-K62929068-001-16-5, Z57245233, 6-Benzylaminopurine, ReagentPlus(R), >=99.0% (HPLC), F0578-0089, 2B76FFBD-3C3A-4349-9047-E5B8945B54A7, ((2r,3s,4r,5r)-5-(4-amino-2-oxopyrimidin-1(2h)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyltriphosph, InChI=1/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)

Application

N6-Benzyladenine is primarily used as a plant growth regulator in tissue culture media to induce shoot formation and enhance axillary bud proliferation. It demonstrates particular efficacy in orchid micropropagation and woody plant tissue cultures. The compound also finds application in delaying post-harvest leaf yellowing in vegetables and cut flowers. Researchers employ this cytokinin analog to study cell cycle regulation and plant developmental processes. Its synthetic nature provides more consistent results than natural plant hormones in experimental systems.

Safety and Hazards

GHS Hazard Statements

• H402: Harmful to aquatic life [Hazardous to the aquatic environment, acute hazard]
• H412: Harmful to aquatic life with long lasting effects [Hazardous to the aquatic environment, long-term hazard]

Precautionary Statements

• P273, and P501

Hazard Classes and Categories

• Acute Tox. 4 (51%)
• Skin Irrit. 2 (52%)
• Eye Irrit. 2 (52%)
• STOT SE 3 (51%)
• Repr. 2 (28%)
• Aquatic Acute 1 (33%)
• Aquatic Chronic 2 (29%)

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.