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Merck
CN

D7674

Sigma-Aldrich

6-(γ,γ-二甲基烯丙胺)嘌呤

BioReagent, suitable for plant cell culture, ≥98.5%

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别名:
2iP, N6-(2-异戊烯基)腺嘌呤
经验公式(希尔记法):
C10H13N5
CAS号:
分子量:
203.24
MDL编号:
UNSPSC代码:
10171502
PubChem化学物质编号:
NACRES:
NA.72

产品线

BioReagent

质量水平

检测方案

≥98.5%

形式

powder

技术

cell culture | plant: suitable

应用

agriculture

储存温度

−20°C

SMILES字符串

C\C(C)=C\CNc1ncnc2[nH]cnc12

InChI

1S/C10H13N5/c1-7(2)3-4-11-9-8-10(13-5-12-8)15-6-14-9/h3,5-6H,4H2,1-2H3,(H2,11,12,13,14,15)

InChI key

HYVABZIGRDEKCD-UHFFFAOYSA-N

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应用

6-(γ,γ-二甲基烯丙基氨基)嘌呤已被用作Murashige和Skoog培养基的成分,以促进斐济果中组织的木质化 ,并作为SIM培养基的成分,用于子叶的再生。
6-(γ,γ-二甲基烯丙基氨基)嘌呤(2iP)是一种细菌衍生的核糖苷细胞分裂素,被用于植物组织的生长,例如烟草和大豆愈伤组织。 2iP是细胞分裂素玉米素的前体。2iP已被用于Schenk和Hildebrandt培养基以支持体外 Genista植物芽尖的微芽培养物的繁殖。

生化/生理作用

6-(γ,γ-二甲基烯丙基氨基)嘌呤(2iP)是一种细菌衍生的核糖苷细胞分裂素,被用于植物组织的生长,例如烟草和大豆愈伤组织。2iP是细胞分裂素玉米素的前体。2iP被用于Schenk和Hildebrandt培养基以支持 体外 Genista植物芽尖的微芽培养物的繁殖。

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

法规信息

农药列管产品

分析证书(COA)

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6-gamma, gamma-Dimethylallylamino) purine as a precursor of zeatin
Miura GA and Miller CO
Plant Physiology, 44(3), 372-376 (1969)
In vitro propagation of Guayabo del pais(Acca sellowiana (Berg.) Burret)
Ross S and Grasso R
Fruit, Vegetable and Cereal Science and Biotechnology, 4, 83-87 (2010)
The shoot regeneration capacity of excised Arabidopsis cotyledons is established during the initial hours after injury and is modulated by a complex genetic network of light signalling
Nameth B, et al.
Plant, Cell and Environment, 36(1), 68-86 (2013)
J P Helgeson et al.
Plant physiology, 44(2), 193-198 (1969-02-01)
The growth rates of tobacco callus tissues on media containing 10(-6) to 10 mum 6-(gamma,gamma-dimethylallylamino)purine (2iP) were measured. At concentrations of 10(-4) mum and above growth rates were exponential and dependent on cytokinin concentration. At 2iP concentrations of 10(-4) to
E Strzelczyk et al.
Acta microbiologica Polonica, 34(2), 177-185 (1985-01-01)
Studies on the effect of post culture liquids of actinomycetes on cytokinin-like substances production by mycorrhizal fungi have revealed that actinomycete metabolites inhibited or stimulated the synthesis of these compounds. The results of chromatographic analyses suggest, that substances stimulating the

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