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Atomfair Kinetin C10H9N5O CAS 525-79-1
Kinetin (CAS No. 525-79-1), also known as N -(furan-2-ylmethyl)-7 H -purin-6-amine, is a naturally occurring cytokinin plant growth regulator with the molecular formula C10H9N5O. This bioactive purine derivative plays a crucial role in promoting cell division, delaying senescence, and enhancing plant morphogenesis. With a purity grade suitable for research applications, our Kinetin is rigorously tested via HPLC and NMR to ensure optimal quality and consistency. Ideal for plant tissue culture, phytochemical studies, and agricultural research, this compound is supplied as a white to off-white crystalline powder with high solubility in dilute alkaline solutions and organic solvents like DMSO. Store in…
Description
Kinetin (CAS No. 525-79-1), also known as N-(furan-2-ylmethyl)-7H-purin-6-amine, is a naturally occurring cytokinin plant growth regulator with the molecular formula C10H9N5O. This bioactive purine derivative plays a crucial role in promoting cell division, delaying senescence, and enhancing plant morphogenesis. With a purity grade suitable for research applications, our Kinetin is rigorously tested via HPLC and NMR to ensure optimal quality and consistency. Ideal for plant tissue culture, phytochemical studies, and agricultural research, this compound is supplied as a white to off-white crystalline powder with high solubility in dilute alkaline solutions and organic solvents like DMSO. Store in a cool, dry environment to maintain stability.
Properties
- CAS Number: 525-79-1
- Complexity: 239
- IUPAC Name: N-(2-furylmethyl)-7H-purin-6-amine
- InChI: InChI=1S/C10H9N5O/c1-2-7(16-3-1)4-11-9-8-10(13-5-12-8)15-6-14-9/h1-3,5-6H,4H2,(H2,11,12,13,14,15)
- InChI Key: QANMHLXAZMSUEX-UHFFFAOYSA-N
- Exact Mass: 215.08070993
- Molecular Formula: C10H9N5O
- Molecular Weight: 215.21
- SMILES: C1=COC(=C1)CNC2=NC=NC3=C2NC=N3
- Topological: 79.6
- Monoisotopic Mass: 215.08070993
- Physical Description: Solid; White powder;
- Color/Form: Platelets from absolute ethanol
- Melting Point: 266-267 ยฐC
- Solubility: Slightly soluble in cold water, methanol, ethanol. Freely soluble in dilute aqueous hydrochloric acid or sodium hydroxide.
- Dissociation Constants: pKa1 = 2.7; pKa2 = 9.9
- Synonyms: kinetin, 6-Furfurylaminopurine, 6-Furfuryladenine, 6-(Furfurylamino)purine, N6-Furfuryladenine, Cytokinin, N-Furfuryladenine, N-(furan-2-ylmethyl)-7H-purin-6-amine, 1H-PURIN-6-AMINE, N-(2-FURANYLMETHYL)-, N6-(Furfurylamino)purine, Adenine, N-furfuryl-, Furfuryl(purin-6-yl)amine, Cytex, Kinetin (VAN), N(sup 6)-Furfuryladenine, n(6)-furfuryladenine, Caswell No. 272D, 2-Furanmethanamine, N-1H-purin-6-yl-, N-(2-Furanylmethyl)-1H-purin-6-amine, NSC 23119, N-(2-Furylmethyl)-9H-purin-6-amine, N(sup 6)-(Furfurylamino)purine, HSDB 7429, 9H-Purin-6-amine, N-(2-furanylmethyl)-, EINECS 208-382-2, n-furfuryl-Adenine, NSC-23119, EPA Pesticide Chemical Code 116801, UNII-P39Y9652YJ, DTXSID9035175, CHEBI:27407, P39Y9652YJ, KINETIN [HSDB], KINETIN [MI], KINETIN [MART.], KINETIN [WHO-DD], N-(2-furylmethyl)-1H-purin-6-amine, N(6)-(furfurylamino)purine, 6-[(Furan-2-ylmethyl)amino]-9H-purine, Furan-2-ylmethyl-(9H-purin-6-yl)-amine, DTXCID7015175, N-1H-purin-6-yl-2-Furanmethanamine, Furan-2-ylmethyl-(9H-purin-6-yl)-amin, KINETIN (MART.), N-(2-furylmethyl)-N-(9H-purin-6-yl)amine, 6-((Furan-2-ylmethyl)amino)-9H-purine, 6 furfurylaminopurine, NFurfuryladenine, 6Furfuryladenine, N6Furfuryladenine, 6 Furfuryladenine, Adenine, Nfurfuryl, 6(Furfurylamino)purine, Furfuryl(purin6yl)amine, N6(Furfurylamino)purine, KINETIN [INCI], N(sup 6)Furfuryladenine, 6-furfurylamino-9H-purine, N(sup 6)(Furfurylamino)purine, 2Furanmethanamine, N1Hpurin6yl, N(2Furanylmethyl)1Hpurin6amine, CHEBI:23530, DTXSID30109212, 1HPurin6amine, N(2furanylmethyl), 9HPurin6amine, N(2furanylmethyl), USEPA/OPP Pesticide Code: 116802, 69235-69-4, qanmhlxazmsuex-uhfffaoysa-n, 525-79-1, N-(furan-2-ylmethyl)-9H-purin-6-amine, Kinetin (6-Furfuryladenine), MFCD00075757, MLS000101228, CHEMBL228792, (2-furylmethyl)purin-6-ylamine, 6046-79-3, 6-Furfuryladenine;N6-Furfuryladenine, CAS-525-79-1, SMR000017633, N-(furan-2-ylmethyl)-1H-purin-6-amine, SR-01000622725, Kinerase, H35, Prestwick_965, Spectrum_001064, 2uy5, N6FFA, Kinetin, 99.0%, N(Sup6)-Furfuryladenine, Maybridge1_007141, Prestwick0_000659, Prestwick1_000659, Prestwick2_000659, Prestwick3_000659, Spectrum2_001364, Spectrum3_000610, Spectrum4_000820, Spectrum5_001599, cid_3830, Oprea1_761931, SCHEMBL15705, SCHEMBL15706, SCHEMBL23818, US9138393, Kinetin, US9144538, Kinetin, BSPBio_000697, BSPBio_002120, KBioGR_001339, KBioSS_001544, 6-Purinylamine, N-furfuryl-, MLS006011916, DivK1c_000011, SPECTRUM1500764, SPBio_001288, SPBio_002618, BPBio1_000767, N(Sup6)-(Furfurylamino)purine, SCHEMBL23014706, BDBM39302, HMS500A13, HMS561M13, KBio1_000011, KBio2_001544, KBio2_004112, KBio2_006680, KBio3_001620, NINDS_000011, BDBM181147, GLXC-20307, HMS1570C19, HMS1921G18, HMS2097C19, HMS2231E12, HMS3369D11, HMS3651K18, HMS3714C19, HMS5080B10, HMS5204B05, Kinetin, >=99.0% (HPLC), ALBB-020727, HY-N0160, NSC23119, TNP00302, Tox21_301214, AC2491, CCG-38842, GEO-04254, s2316, SBB005348, STK944589, 2-Furylmethyl-(7H-purin-6-yl)amine, AKOS000266263, AKOS008967503, AKOS025395637, N-(2-furylmethyl)-3h-purin-6-amine, AB02897, CCG-208509, CS-1567, DB11336, FF01915, KS-5279, SDCCGMLS-0066627.P001, IDI1_000011, N-(2-furanylmethyl)-7H-purin-6-amine, N-(2-furanylmethyl)-1h-purine-6 amine, NCGC00016488-01, NCGC00016488-02, NCGC00016488-03, NCGC00016488-04, NCGC00016488-05, NCGC00016488-06, NCGC00016488-07, NCGC00016488-08, NCGC00016488-09, NCGC00016488-10, NCGC00094553-01, NCGC00094553-02, NCGC00094553-03, NCGC00094553-04, NCGC00094553-05, NCGC00094553-06, NCGC00255418-01, AC-11023, Kinetin, Vetec(TM) reagent grade, 99%, N-(2-Furylmethyl)-9H-purin-6-amine #, SMR003472578, ST057262, SY010745, N-[(Fur-2-yl)methyl]-9H-purin-6-amine, DB-318128, furan-2-yl-methyl-(7H-purin-6-yl)-amine, N-[(furan-2-yl)methyl]-7H-purin-6-amine, AB00052172, K0009, NS00013804, SW197051-3, C08272, EN300-378089, Kinetin, plant cell culture tested, crystalline, AB00052172-13, SR-01000637138, N-[(FURAN-2-YL)METHYL]-9H-PURIN-6-AMINE, Q2251215, SR-01000622725-3, SR-01000622725-4, SR-01000637138-1, SR-01000637138-2, BRD-K65667145-001-05-8, BRD-K65667145-001-07-4, BRD-K65667145-001-14-0, Kinetin;N6-Furfuryladenine;Furfuryl(purin-6-yl)amine, F0578-0087, Z372953774, Kinetin, BioReagent, plant cell culture tested, amorphous powder
Application
Kinetin is widely used in plant biology research to study cytokinin-mediated processes such as cell division, shoot initiation, and leaf senescence. It is applied in tissue culture protocols to enhance callus growth and organogenesis in various plant species. Researchers also utilize Kinetin to investigate anti-aging effects in both plant and animal model systems.
Safety and Hazards
GHS Hazard Statements
- H341 (87.1%): Suspected of causing genetic defects [Warning Germ cell mutagenicity]
Precautionary Statements
- P203, P280, P318, P405, and P501
Hazard Classes and Categories
- Muta. 2 (87.1%)
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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.
Disclaimer
Intended Use & Restrictions
This product is sold exclusively for laboratory research, analytical testing, or non-commercial purposes.
- Strictly prohibited: Resale, repackaging, or formulation into commercial products.
- Not approved for human/animal use, diagnostics, or manufacturing (including pharmaceuticals, agrochemicals, or consumer goods).
Patent & Regulatory Compliance
Certain molecules may be protected by active patents or regulatory restrictions.
- Buyers must independently verify patent status (e.g., via USPTO/EPO/CNIPA) and comply with local laws.
- Atomfair LLC does not provide legal assurances regarding patent non-infringement or jurisdictional compliance.
Liability Release
By purchasing, the buyer agrees to:
- Use this product only as permitted by law.
- Indemnify Atomfair LLC against all claims arising from misuse, patent infringement, or regulatory violations.
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