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About This Item
Empirical Formula (Hill Notation):
C15H21N5O5
CAS Number:
Molecular Weight:
351.36
UNSPSC Code:
10171502
NACRES:
NA.72
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5460894
Assay:
~95%
Biological source:
synthetic (organic)
Form:
powder
Solubility:
glacial acetic acid: 50 mg/mL, clear, colorless to faintly yellow
Storage temp.:
−20°C
biological source
synthetic (organic)
Quality Segment
product line
BioReagent
assay
~95%
form
powder
technique(s)
cell culture | plant: suitable
solubility
glacial acetic acid: 50 mg/mL, clear, colorless to faintly yellow
application(s)
agriculture
storage temp.
−20°C
SMILES string
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
InChI key
GOSWTRUMMSCNCW-HNNGNKQASA-N
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.
Biochem/physiol Actions
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
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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