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Benzyladenine

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Name

Benzyladenine

EINECS 214-927-5
CAS No. 1214-39-7 Density 1.393 g/cm3
PSA 66.49000 LogP 2.03800
Solubility soluble in water Melting Point 229-233 °C
Formula C12H11N5 Boiling Point 529.388 °C at 760 mmHg
Molecular Weight 225.253 Flash Point 273.964 °C
Transport Information UN 2348 3/PG 3 Appearance white to light yellow crystalline powder
Safety 9-24/25-36/37/39-26-23 Risk Codes 36/37/38-20/21/22
Molecular Structure Molecular Structure of 1214-39-7 (Benzyladenine) Hazard Symbols IrritantXi,HarmfulXn
Synonyms

6-Benzylamino Purine;6-Benzylaminopurine ( 6-BA);Benzylaminopurine;6-Benzylaminopurine (6BA);6-Benzyl Adenine(6-Benzyl Aminopurine);6-Benzylaminopurine;BA;6-Benzylaminopurine *;6-Benzylamino purine (6-BA);N-benzyl-7H-purin-6-amine;Paturyl;N-Benzyl-9H-purin-6-amine;N-(Phenylmethyl)-1H-purin-6-amine;BA (growth stimulator);6-(Benzylamino)purine;Prestwick_414;6-Benzylaminopurine (6-BA);N6-Benzyladenine;BAP (growth stimulant);N(6)-Benzylaminopurine;1H-Purin-6-amine,N-(phenylmethyl)-;Aminopurine, 6-benzyl;6-Benzyl Aminopurine;6-benzylaminopurine BA;6-(n-Benzyl) Aminopurin;N-6-Benzyladenine;benzyl(purin-6-yl)amine;9H-Purin-6-amine, N-(phenylmethyl)-;

Article Data 54

Benzyladenine Synthetic route

87-42-3

6-chloropurine

100-46-9

benzylamine

1214-39-7

6-benzyladenine

Conditions
ConditionsYield
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; Microwave irradiation; regioselective reaction;93%
4294-16-0

N6-Benzyladenosine

1214-39-7

6-benzyladenine

Conditions
ConditionsYield
With hydrogenchloride In water at 100℃; for 3h; Reagent/catalyst; Temperature;92%

phenylmagnesium bromide

111098-24-9

Benzotriazol-1-ylmethyl-(9H-purin-6-yl)-amine

1214-39-7

6-benzyladenine

Conditions
ConditionsYield
In diethyl ether at 25℃; for 16h;80%
19769-32-5

6-methylsulfonylpurine

100-46-9

benzylamine

1214-39-7

6-benzyladenine

Conditions
ConditionsYield
In butan-1-ol for 0.75h; Substitution;78.2%

7-benzyl-6-benzylamino-2-chloropurine

1214-39-7

6-benzyladenine

Conditions
ConditionsYield
With potassium hydroxide; hydrogen; palladium on activated charcoal In ethanol under 760 Torr; for 15h; Hydrogenation;69%
7387-58-8, 80007-24-5

6-N-2',3',5'-tri-O-tetraacetyladenosine

A

1214-39-7

6-benzyladenine

B

18646-11-2

α-D-ribofuranosyl-1-phosphate

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: potassium carbonate / N,N-dimethyl-formamide / 20 h / 20 °C
2: methanol; ammonia / 48 h / 20 °C
3: potassium dihydrogenphosphate; Escherichia coli purine nucleoside phosphorylase / 37 °C / pH 7.5 / aq. buffer; Enzymatic reaction
View Scheme
1338578-76-9

N6-acetyl-2',3',5'-tri-O-acetyl-N6-benzyladenosine

A

1214-39-7

6-benzyladenine

B

18646-11-2

α-D-ribofuranosyl-1-phosphate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: methanol; ammonia / 48 h / 20 °C
2: potassium dihydrogenphosphate; Escherichia coli purine nucleoside phosphorylase / 37 °C / pH 7.5 / aq. buffer; Enzymatic reaction
View Scheme
100-39-0

benzyl bromide

1214-39-7

6-benzyladenine

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: potassium carbonate / N,N-dimethyl-formamide / 20 h / 20 °C
2: methanol; ammonia / 48 h / 20 °C
3: potassium dihydrogenphosphate; Escherichia coli purine nucleoside phosphorylase / 37 °C / pH 7.5 / aq. buffer; Enzymatic reaction
View Scheme
4294-16-0

N6-Benzyladenosine

A

1214-39-7

6-benzyladenine

B

18646-11-2

α-D-ribofuranosyl-1-phosphate

Conditions
ConditionsYield
With Escherichia coli purine nucleoside phosphorylase at 25℃; pH=7.5; Kinetics; aq. phosphate buffer; Enzymatic reaction;
With potassium dihydrogenphosphate; Escherichia coli purine nucleoside phosphorylase at 37℃; pH=7.5; Equilibrium constant; aq. buffer; Enzymatic reaction;

Benzyladenine Consensus Reports

Reported in EPA TSCA Inventory.

Benzyladenine Specification

The Benzyladenine, with the CAS registry number 1214-39-7, is also known as Benzyl(purin-6-yl)amine. It belongs to the product categories of Pharmaceutical Raw Materials; Miscellaneous; Purine; Amines; Biochemistry; Cytokinins; Nucleobases and their analogs; Nucleosides, Nucleotides & Related Reagents; Plant Growth Regulators; Plant Hormones. Its EINECS number is 214-927-5. This chemical's molecular formula is C12H11N5 and molecular weight is 225.25. What's more, its systematic name is N-Benzyl-7H-purin-6-amine. Its classification codes are: (1)Agricultural Chemical; (2)Growth Substances; (3)Growth regulator / Fertilizer; (4)Mutation data; (5)Plant growth regulators. This chemical should be sealed and stored in a cool and dry place. Moreover, it should be protected from oxides. This substance is a first-generation synthetic cytokinin that elicits plant growth and development responses, setting blossoms and stimulating fruit richness by stimulating cell division. It is an inhibitor of respiratory kinase in plants, and increases post-harvest life of green vegetables.

Physical properties of Benzyladenine are: (1)ACD/LogP: 2.164; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 2.15; (4)ACD/LogD (pH 7.4): 2.16; (5)ACD/BCF (pH 5.5): 25.36; (6)ACD/BCF (pH 7.4): 25.92; (7)ACD/KOC (pH 5.5): 349.77; (8)ACD/KOC (pH 7.4): 357.43; (9)#H bond acceptors: 5; (10)#H bond donors: 2; (11)#Freely Rotating Bonds: 2; (12)Polar Surface Area: 66.49 Å2; (13)Index of Refraction: 1.766; (14)Molar Refractivity: 66.899 cm3; (15)Molar Volume: 161.701 cm3; (16)Polarizability: 26.521×10-24cm3; (17)Surface Tension: 80.4 dyne/cm; (18)Density: 1.393 g/cm3; (19)Flash Point: 273.964 °C; (20)Enthalpy of Vaporization: 80.442 kJ/mol; (21)Boiling Point: 529.388 °C at 760 mmHg; (22)Vapour Pressure: 0 mmHg at 25°C.

Preparation: this chemical can be prepared by 7(9)H-purin-6-ylamine and phenylmethanol; sodium salt at the temperature of 130 °C. The reaction time is 17 hours. The yield is about 55%.

Benzyladenine can be prepared by 7(9)H-purin-6-ylamine and phenylmethanol; sodium salt at the temperature of 130 °C

Uses of Benzyladenine: it can be used to produce by benzyl-(1-oxy-9H-purin-6-yl)-amine at the temperature of 30 °C. It will need regent MCPBA and solvent methanol with the reaction time of 20 hours. The yield is about 35%.

Benzyladenine can be used to produce by benzyl-(1-oxy-9H-purin-6-yl)-amine at the temperature of 30 °C

When you are using this chemical, please be cautious about it as the following:
This chemical is harmful by inhalation, in contact with skin and if swallowed. It is irritating to eyes, respiratory system and skin. You must avoid contact with skin and eyes. In case of contact with eyes, you should rinse immediately with plenty of water and seek medical advice. You should keep the container in a well-ventilated place. You must not breathe gas/fumes/vapour/spray (appropriate wording to be specified by the manufacturer). When using it, you need wear suitable protective clothing, gloves and eye/face protection.

You can still convert the following datas into molecular structure:
(1)SMILES: n1c(c2c(nc1)ncn2)NCc3ccccc3
(2)Std. 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)
(3)Std. InChIKey: NWBJYWHLCVSVIJ-UHFFFAOYSA-N

The toxicity data is as follows:  

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 oral 1300mg/kg (1300mg/kg) SENSE ORGANS AND SPECIAL SENSES: LACRIMATION: EYE

BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)
Toho Igakkai Zasshi. Journal of Medical Society of Toho University. Vol. 19, Pg. 336, 1972.
mouse LD50 skin > 5gm/kg (5000mg/kg)   Toho Igakkai Zasshi. Journal of Medical Society of Toho University. Vol. 19, Pg. 336, 1972.
mouse LD50 subcutaneous > 2300mg/kg (2300mg/kg)   Toho Igakkai Zasshi. Journal of Medical Society of Toho University. Vol. 19, Pg. 336, 1972.
rat LD50 oral 2125mg/kg (2125mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

SENSE ORGANS AND SPECIAL SENSES: LACRIMATION: EYE
Toho Igakkai Zasshi. Journal of Medical Society of Toho University. Vol. 19, Pg. 336, 1972.

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