• Product NameN-(Phenylmethyl)-9H-purin-6-amine
  • CasNo. 1214-39-7
  • MFC12H11N5
  • MW225.253
  • Purity
  • Appearancewhite to light yellow crystalline powder
  • Packing
  • Contact usInquiry

Product Details

CasNo: 1214-39-7

MF: C12H11N5

Appearance: white to light yellow crystalline powder

Reputable supplier selling N-(Phenylmethyl)-9H-purin-6-amine 1214-39-7 with stock

  • Molecular Formula:C12H11N5
  • Molecular Weight:225.253
  • Appearance/Colour:white to light yellow crystalline powder 
  • Vapor Pressure:3.3 mm Hg ( 20 °C) 
  • Melting Point:229-233 °C 
  • Refractive Index:n20/D 1.418(lit.)  
  • Boiling Point:529.388 °C at 760 mmHg 
  • PKA:9.36±0.20(Predicted) 
  • Flash Point:273.964 °C 
  • PSA:66.49000 
  • Density:1.393 g/cm3 
  • LogP:2.03800 

Benzyladenine(Cas 1214-39-7) Usage

Preparation

synthesis 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

Health Hazard

6-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.

Trade name

ABG? 3034; ACCEL?; AGTROL?; 6-BA?; BA? (growth stimulant); CHRYSAL BVB?; EXILIS?; PERLAN?; PROMALIN?; SD? 4901; SQ? 4609

Safety Profile

Moderately toxic by ingestion andskin contact. Human mutation data reported. Whenheated to decomposition it emits toxic vapors of NOx.

Potential Exposure

A 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.

Shipping

UN3259 Amines, solid, corrosive, n.o.s, or Polyamines, solid, corrosive, n.o.s., Hazard class: 8; Labels: 8—Corrosive material, Technical Name Required.

Purification Methods

It 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.]

Incompatibilities

May 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 Disposal

Dissolve 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.

Application

6-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.

Definition

ChEBI: 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 Description

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

Agricultural Uses

6-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.

InChI:InChI=1/C12H11N5/c1-2-4-9(5-3-1)6-13-11-10-12(15-7-14-10)17-8-16-11/h1-5,7-8,10H,6H2,(H,13,14,15,16,17)

1214-39-7 Relevant articles

Design and synthesis of purine analogues as highly specific ligands for FcyB, a ubiquitous fungal nucleobase transporter

Lougiakis, Nikolaos,Gavriil, Efthymios-Spyridon,Kairis, Markelos,Sioupouli, Georgia,Lambrinidis, George,Benaki, Dimitra,Krypotou, Emilia,Mikros, Emmanuel,Marakos, Panagiotis,Pouli, Nicole,Diallinas, George

, p. 5941 - 5952 (2016)

In the course of our study on fungal pur...

Structure-based design, synthesis, and antimicrobial activity of purine derived SAH/MTA nucleosidase inhibitors

Tedder, Martina E.,Nie, Zhe,Margosiak, Stephen,Chu, Shaosong,Feher, Victoria A.,Almassy, Robert,Appelt, Krzysztof,Yager, Kraig M.

, p. 3165 - 3168 (2004)

The structure-based design, synthesis, a...

N6-isopentenyladenosine a new potential anti-angiogenic compound that targets human microvascular endothelial cells in vitro

Castiglioni, Sara,Romeo, Valentina,Casati, Silvana,Ottria, Roberta,Perrotta, Cristiana,Ciuffreda, Pierangela,Maier, Jeanette A. M.

, p. 533 - 545 (2018)

N6-isopentenyladenosine is an anti-proli...

-

Skinner,Shive

, p. 6692 (1955)

-

Mechanism of formation of N2-benzylguanine in the reaction of 2-amino- 6-chloropurine with sodium benzyl oxide, and benzylation of nucleic acid bases

Koyama, Ken-Ichi,Hitomi, Kenichi,Terashima, Isamu,Kohda, Kohfuku

, p. 1395 - 1399 (1996)

The mechanism of formation of N2-benzylg...

-

van Eyk,Veldstra

, p. 457,461 (1966)

-

Reactions of Adenine and Its N-Exo Substituted Analogues with Phenyl Glycidyl Ether

Neporozhneva,Studentzsov,Ramsh

, p. 2248 - 2254 (2021/02/12)

Abstract: The features of reactions of a...

Efficient Phosphorus-Free Chlorination of Hydroxy Aza-Arenes and Their Application in One-Pot Pharmaceutical Synthesis

Wang, Jian,Li, Yan-Hui,Pan, Song-Cheng,Li, Ming-Fang,Du, Wenting,Yin, Hong,Li, Jing-Hua

supporting information, p. 146 - 153 (2020/03/10)

The chlorination of hydroxy aza-arenes w...

Chemoenzymatic synthesis of cytokinins from nucleosides: Ribose as a blocking group

Oslovsky, Vladimir E.,Solyev, Pavel N.,Polyakov, Konstantin M.,Alexeev, Cyril S.,Mikhailov, Sergey N.

, p. 2156 - 2163 (2018/03/26)

Nucleoside phosphorylases are involved i...

1214-39-7 Process route

6-chloropurine
87-42-3

6-chloropurine

benzylamine
100-46-9

benzylamine

6-benzyladenine
1214-39-7

6-benzyladenine

Conditions
Conditions Yield
With triethylamine; In ethanol; for 5h; Reflux;
96%
at 100 ℃; for 0.0833333h; microwave irradiation;
95%
With indium(III) chloride; In acetonitrile; at 120 ℃; for 1h; regioselective reaction; Microwave irradiation;
93%
In water; at 100 ℃; for 0.75h; Solvent; Green chemistry;
92%
With triethylamine; In ethanol; Reflux; Inert atmosphere;
82%
With triethylamine; In butan-1-ol; at 110 ℃; for 3h;
69%
With N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; at 110 ℃; for 0.25h; Microwave irradiation;
61%
With N-ethyl-N,N-diisopropylamine; In butan-1-ol; Heating;
In ethanol; Reflux;
With triethylamine; In ethanol; at 80 ℃; for 3h;
7-benzyl-6-benzylamino-2-chloropurine

7-benzyl-6-benzylamino-2-chloropurine

6-benzyladenine
1214-39-7

6-benzyladenine

Conditions
Conditions Yield
With potassium hydroxide; hydrogen; palladium on activated charcoal; In ethanol; for 15h; under 760 Torr;
69%

1214-39-7 Upstream products

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    4005-49-6

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    87-42-3

    6-chloro-7H-purine

  • 100-46-9
    100-46-9

    benzylamine

  • 50-66-8
    50-66-8

    6-(methylthio)-1H-purine

1214-39-7 Downstream products

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    1145787-53-6

    3-(6-benzylamino-purin-9-yl)-butyric acid methyl ester

  • 1145787-55-8
    1145787-55-8

    3-(6-benzylamino-purin-9-yl)-2-methyl-propionic acid vinyl ester

  • 1033400-03-1
    1033400-03-1

    3-(6-benzylamino-purin-9-yl)-propionic acid butyl ester

  • 1145787-52-5
    1145787-52-5

    3-(6-benzylamino-purin-9-yl)-2-methyl-propionic acid methyl ester

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