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D5912

Sigma-Aldrich

6-(γ,γ-Dimethylallylamino)purine

BioReagent, suitable for plant cell culture, ≥90%

Sinonimo/i:

N6 dimethylallyladenine, 2iP, N6-(2-Isopentenyl)adenine

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About This Item

Formula empirica (notazione di Hill):
C10H13N5
Numero CAS:
2365-40-4
Peso molecolare:
203.24
Numero MDL:
MFCD00132998
Codice UNSPSC:
10171502
ID PubChem:
24893984
NACRES:
NA.72

Nome Commerciale

BioReagent

Livello qualitativo

100

Saggio

≥90%

Forma fisica

powder

tecniche

cell culture | plant: suitable

applicazioni

agriculture

Temperatura di conservazione

−20°C

Stringa SMILE

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)
HYVABZIGRDEKCD-UHFFFAOYSA-N

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Categorie correlate

Applicazioni

6-(γ,γ-Dimethylallylamino)purine: has been used as a standard in ultra-high performance liquid chromatography to compare the chromatogram of transgenic and wild type (WT) crude hormone extracts to quantify cytokinin levels, may be used as a component of the Murashige and Skoog (MS) medium for callus culture and in vitro shoot induction, may be used as a supplement in MS medium to make simplified shoot induction medium (SIM) to treat explants for shoot induction

Azioni biochim/fisiol

6-(γ,γ-Dimethylallylamino)purine (2iP) is a bacteria-derived riboside cytokinin used to grow plant tissues such as tobacco and soybean callus. 2iP is a precursor of the cytokinin Zeatin. 2iP can also be used in Schenk and Hildebrandt medium to support in vitro propagation of micro shoot cultures from shoot tips of Genista plants.

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Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

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Wenzislava Ckurshumova et al.
The New phytologist, 204(3), 556-566 (2014-10-03)
In vitro regeneration of complete organisms from diverse cell types is a spectacular property of plant cells. Despite the great importance of plant regeneration for plant breeding and biotechnology, its molecular basis is still largely unclear and many important crop
G A Miura et al.
Plant physiology, 44(3), 372-376 (1969-03-01)
A 6-(gamma,gamma-dimethylallylamino) purine-like compound was found in the culture medium of Rhizopogon roseolus, which had been shown earlier to synthesize zeatin. The role of 6-(gamma,gamma-dimethylallylamino) purine as a precursor of zeatin was studied. Rhizopogon was furnished with 6-(gamma,gamma-dimethylallylamino) purine-8-(14)C. Cochromatography
Maria Luczkiewicz et al.
Zeitschrift fur Naturforschung. C, Journal of biosciences, 60(7-8), 557-566 (2005-09-17)
A two-stage method for in vitro propagation of six Genista species from shoot tips was developed. Multiple microshoot cultures were obtained by growing the shoot tip explants on Schenk and Hildebrandt medium supplemented with 9.84 microM 6-(gamma,gamma-dimethylallylamino)-purine and 0.99 microM
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
Chieh-Han Pu et al.
Journal of food and drug analysis, 26(2), 637-648 (2018-03-24)
A multiresidue analytical method was developed for grapes for the following 24 plant growth regulators: 1-naphthylacetamide, 2,3,5-triiodobenzoic acid, 2,4,5-T, 2-naphthoxyacetic acid, 3-indolylacetic acid, 4-(3-indolyl)-butyric acid, 4-chlorophenoxyacetic acid, 4-nitrophenol, 6-benzylaminopurine, N6-isopentenyladenine, butralin, chlormequat chloride, chlorphonim-Cl, cloprop, forchlorfenuron, gibberellic acid 3, gibberellic acid
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