6-Benzylaminopurine

6-Benzylaminopurine Basic information
Product Name:6-Benzylaminopurine
Synonyms:6-BENZYLAMINOPURINERESEARCH GRADE;6-Benzylaminopurine,BA, N6-Benzyladenine;6-BenzylaMinopurine, 99% 5GR;6-Benzyil AMinopurine;6-benzyl-6H-purin-6-aMine;6-BenzylaMino Purine Tech;6-(Benzylamino)-9H-purine;N-Benzyl-9H-purin-6-amine, N-(9H-Purin-6-yl)benzylamine
CAS:1214-39-7
MF:C12H11N5
MW:225.25
EINECS:214-927-5
Product Categories:Biochemistry;Cytokinins;Nucleobases and their analogs;Nucleosides, Nucleotides & Related Reagents;Plant Growth Regulators;Plant Hormones;Pharmaceutical Raw Materials;Miscellaneous;Purine;Amines;PLANT GROWTH REGULATOR;plantgrowth;1214-39-7;Elisa Kit-plant ELISA Kit
Mol File:1214-39-7.mol
6-Benzylaminopurine Structure
6-Benzylaminopurine Chemical Properties
Melting point 230-233 °C
Boiling point 145 °C(lit.)
density 0.899 g/mL at 20 °C
vapor density >1 (vs air)
vapor pressure 3.3 mm Hg ( 20 °C)
refractive index n20/D 1.418(lit.)
Fp 103 °F
storage temp. 2-8°C
solubility H2O: soluble
pka9.36±0.20(Predicted)
form Liquid
color White to very faint yellow
OdorCharacteristic acrylic.
Water Solubility Soluble in water, methanol and acetone. Slightly soluble in ethyl acetate and dichloromethane and toluene. Insoluble in n-hexane.
BRN 19406
Stability:Stable. Incompatible with strong oxidizing agents.
InChIKeyNWBJYWHLCVSVIJ-UHFFFAOYSA-N
LogP1.570
CAS DataBase Reference1214-39-7(CAS DataBase Reference)
NIST Chemistry Reference1H-purin-6-amine, n-(phenylmethyl)-(1214-39-7)
EPA Substance Registry SystemN-Benzyladenine (1214-39-7)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-20/21/22-22
Safety Statements 9-24/25-37/39-26-36-23
RIDADR UN 2348 3/PG 3
WGK Germany 3
RTECS UD3150000
8
TSCA Yes
HS Code 29335995
Hazardous Substances Data1214-39-7(Hazardous Substances Data)
ToxicityLD50 orl-rat: 2125 mg/kg TOIZAG 19,336,72
MSDS Information
ProviderLanguage
N-Benzyl-adenine English
ACROS English
SigmaAldrich English
ALFA English
6-Benzylaminopurine Usage And Synthesis
Chemical PropertiesColorless to off-white or yellow powder. Corrosive. Insoluble in water, slightly soluble in ethanol, stable in acid and alkali.
Uses6-Benzylaminopurine is a plant growth regulator that belongs to the class of first generation synthetic cytokinin used in agriculture.
6-Benzylaminopurine has been used:
to induce sprouting in plant materials.
in seed germination medium for culturing of seeds.
to modify Murashige and Skoog (MS) media for shoot initiation.
inhibitor of respiratory kinase in plants.
6-Benzylaminopurine, benzyl adenine (BAP) is a synthetic cytokinin which together with auxins elicits plant growth and development responses. BAP is a widely use cytokinin supplement to plant growth media such as Murashige and Skoog medium, Gamborg’s medium, and Chu’s N6 medium.
Application6-Benzylaminopurine solution has been used as a component in the Murashige & Skoog medium (MS) for culturing mandarin explants and plantlets of Dendrocalamus asper (Schultes f.). It has also been used as a supplement in Nitsch and Nitsch medium (NN) of grapevine explants.
Preparationsynthesis of 6-benzylaminopurine: To 5g hypoxanthine, add 20mL SOCl2, 0.25g DMAP, 10gBTC dissolved in 20mL SOCl2. Heat and add BTC/SOCl2 dropwise. Reflux (refrigerant cooling) to complete dissolution, steam out SOCl2 (containing phosgene, which is used for recovery), evaporated (drained), cooled to room temperature to obtain a milky yellow solid (6-chloropurine and DMAP.Hcl). Directly add 4g benzylamine and 25g triethylamine to it, heat to 70~80 ℃, or microwave heating, until the 6-chloropurine reaction is complete (TLC monitoring), add ethanol, the solid filtered out is washed with ethanol, and dried to obtain 7 g of product 6-benzylaminopurine with a brown color.
Preparation and biological activity of 6-benzylaminopurine derivatives in plants and human cancer cells
DefinitionChEBI: 6-Benzylaminopurine is a member of the class of 6-aminopurines that is adenine in which one of the hydrogens of the amino group is replaced by a benzyl group. It has a role as a plant metabolite and a cytokinin. It derives from an adenine.
General Description6-Benzylaminopurine is a plant growth regulator that belongs to the class of first generation synthetic cytokinin used in agriculture commodities.
Health Hazard6-benzylaminopurine (6-BA) is widely used in agriculture and horticulture as plant growth regulator. Its excessive use may pose a potential risk to both environment and human health, which is causing great concern. Vapor is irritating when breathed at high concentrations. Contact with liquid causes irritation of skin and burning of eyes; Vapors cause a slight smarting of the eyes or respiratory system if present in high concentrations; If spilled on clothing and allowed to remain, may cause smarting and reddening of the skin.
Agricultural Uses6-Benzylaminopurine is a plant growth promoter, is the first applied synthetic cytokinin, mainlyused as a broad- spectrum plant growth regulator. It can be used inagriculture, horticulture, for plants at different stages, from germination to harvest. It enhance the shape of apples and to increase the fruit set in pears. It increases the yield of pistachios and tomatoes. Not listed for use in EU countries. Registered for use in the U.S.
Trade nameABG® 3034; ACCEL®; AGTROL®; 6-BA®; BA® (growth stimulant); CHRYSAL BVB®; EXILIS®; PERLAN®; PROMALIN®; SD® 4901; SQ® 4609
Safety ProfileModerately toxic by ingestion andskin contact. Human mutation data reported. Whenheated to decomposition it emits toxic vapors of NOx.
Potential ExposureA polyamine plant growth regulator used to lengthen and enhance the shape of apples and to increase the fruit set in pears. It increases the yield of pistachios and tomatoes. Not listed for use in the EU countries.
ShippingUN3259 Amines, solid, corrosive, n.o.s, or Polyamines, solid, corrosive, n.o.s., Hazard class: 8; Labels: 8—Corrosive material, Technical Name Required.
Purification MethodsIt is purified by recrystallisation from aqueous EtOH. It has at 207 and 270nm (H2O), 268 nm max (pH 6), 274nm (0.1 N HCl) and 275nm (0.1 N NaOH). [Daly J Org Chem 21 1553 1956, Bullock et al. J Am Chem Soc 78 3693 1956, Beilstein 26 III/IV 3575.]
IncompatibilitiesMay react with strong oxidizers such as chlorates, peroxides, nitrates, etc. May release heat on contact with water. Solid and corrosive amines are chemical bases. Neutralize acids to form salts plus water in exothermic reactions. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. May generate flammable gaseous hydrogen in combination with strong reducing agents, such as hydrides.
Waste DisposalDissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed.
Acetaminophen Benzyltriethylammonium chloride EC 2.6.1.2 BZ-DMT-DEOXYADENOSINE 2-CLPH DIESTER TRIETHYLAMMONIUM SALT N6-BENZYLADENOSINE N6,3'-O-DIBENZOYL-2'-DEOXYADENOSINE N-Ethylmethylamine Triethylamine 5'-O-(4,4'-Dimethoxytrityl)-N6-benzoyl-2'-deoxyadenosine-3'-(2-cyanoethyl-N,N-diisopropyl)phosphoramidite Sulfamic acid Purine N-Benzoylaminopurine Bis(2-ethylhexyl)amine Benzyl Benzyl benzoate Benzyl nicotinate N6-Benzoyl-2'-deoxyadenosine Triethanolamine

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