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Z3541

Sigma-Aldrich

trans-Zeatin-riboside

suitable for plant cell culture, BioReagent, ~95%

Synonym(s):

9-(β-D-Ribofuranosyl)-trans-zeatin, N6-(trans-4-Hydroxy-3-methyl-2-buten-1-yl)adenosine

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About This Item

Empirical Formula (Hill Notation):
C15H21N5O5
CAS Number:
6025-53-2
Molecular Weight:
351.36
Beilstein/REAXYS Number:
5460894
MDL number:
MFCD00036809
UNSPSC Code:
10171502
PubChem Substance ID:
24902179
NACRES:
NA.72
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product line

BioReagent

assay

~95%

technique(s)

cell culture | plant: suitable

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

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1 of 4

This Item
PHR3046PHR1957PHR2118
Formoterol Fumarate certified reference material, pharmaceutical secondary standard

PHR2703

Formoterol Fumarate

Metoprolol Fumarate pharmaceutical secondary standard, certified reference material

PHR3046

Metoprolol Fumarate

Tenofovir disoproxil fumarate Pharmaceutical Secondary Standard; Certified Reference Material

PHR1957

Tenofovir disoproxil fumarate

Dimethyl Fumarate Pharmaceutical Secondary Standard; Certified Reference Material

PHR2118

Dimethyl Fumarate

grade

certified reference material, pharmaceutical secondary standard

grade

certified reference material, pharmaceutical secondary standard

grade

certified reference material, pharmaceutical secondary standard

grade

certified reference material, pharmaceutical secondary standard

form

solid

form

-

form

-

form

-

application(s)

pharmaceutical small molecule

application(s)

pharmaceutical

application(s)

pharmaceutical

application(s)

pharmaceutical small molecule

agency

traceable to Ph. Eur. F0372000

agency

traceable to USP 1441287

agency

traceable to USP 1643656

agency

-

description

Pharmaceutical Secondary Standard; Certified Reference Material

description

-

description

-

description

-

API family

formoterol 

API family

metoprolol

API family

tenofovir

API family

dimethyl fumarate

Application

Trans-Zeatin-riboside has been used to treat the crystals, retrieved from the capillaries for crystallization.[1] It has also been used as a supplement in Murashige and Skoog (MS) medium to form shoot induction medium.[2]

Biochem/physiol Actions

Trans-zeatin-riboside is a kind of cytokinin precursor, which is an important long-distance signalling form in xylem vessels.[3] It serves as an inhibitory factor in root xylem sap by negatively modulating adventitious root formation.[4]
Koenig RL; Morris RO; Polacco JC

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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    Certificates of Analysis (COA)

    Lot/Batch Number
    WXBD5019V
    WXBD1481V
    WXBD1220V
    BGBC3036
    BGBB9268

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    Spencer LT, et al.
    Tissue processing 6." Bancroft's Theory and Practice of Histological Techniques, Expert Consult: Online and Print, 7: Bancroft's Theory and Practice of Histological Techniques, 107-107 (2013)
    Voltammetric Analysis on the Formation of Fe (OH)2 and FeCO3, and on the Reactivity of Passivation of Steel in Carbonate Solutions.
    Eliyan FF, et al.
    Journal of Materials Engineering and Performance, 24(6), 2473-2480 (2015)
    Selection of highly effective rectification regimes for ethyl alcohol.
    Vyaz'mina NA and Baranov DA.
    Chemical and Petroleum Engineering, 42(9), 494-502 (2006)
    Surrogate alcohol: what do we know and where do we go?
    Lachenmeier DW, et al.
    Alcoholism, Clinical and Experimental Research, 31(10), 1613-1624 (2007)
    Sodium hydroxide-catalyzed transfer hydrogenation of carbonyl compounds and nitroarenes using ethanol or isopropanol as both solvent and hydrogen donor.
    Wang D, et al.
    J. Mol. Catal. A: Chem., 400, 14-21 (2015)
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