Z3541

trans-Zeatin-riboside

suitable for plant cell culture, BioReagent, ~95%

• Synonyme(s) : 9-(β-D-Ribofuranosyl)-trans-zeatin, N⁶-(trans-4-Hydroxy-3-methyl-2-buten-1-yl)adenosine
• Formule empirique (notation de Hill): C₁₅H₂₁N₅O₅
• Numéro CAS: 6025-53-2
• Poids moléculaire : 351.36
• Numéro Beilstein : 5460894
• Numéro MDL: MFCD00036809
• Code UNSPSC : 10171502
• ID de substance PubChem : 24902179
• Nomenclature NACRES : NA.72

Propriétés

• Gamme de produits: BioReagent
• Pureté: ~95%
• Technique(s): cell culture | plant: suitable
• Application(s): agriculture
• Température de stockage: −20°C
• Chaîne SMILES: C\C(CO)=C/CNc1ncnc2n(cnc12)[C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O
• InChI: 1S/C15H21N5O5/c1-8(4-21)2-3-16-13-10-14(18-6-17-13)20(7-19-10)15-12(24)11(23)9(5-22)25-15/h2,6-7,9,11-12,15,21-24H,3-5H2,1H3,(H,16,17,18)/b8-2+/t9-,11-,12-,15-/m1/s1
• Clé InChI: GOSWTRUMMSCNCW-HNNGNKQASA-N

Description

Application

Trans-Zeatin-riboside has been used to treat the crystals, retrieved from the capillaries for crystallization. It has also been used as a supplement in Murashige and Skoog (MS) medium to form shoot induction medium.

Actions biochimiques/physiologiques

Trans-zeatin-riboside is a kind of cytokinin precursor, which is an important long-distance signalling form in xylem vessels. It serves as an inhibitory factor in root xylem sap by negatively modulating adventitious root formation.

Koenig RL; Morris RO; Polacco JC

Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable
• Équipement de protection individuelle: Eyeshields, Gloves, type N95 (US)