| Identification | Back Directory | [Name]
6-(4-Hydroxy-3-methylbutylamino)-9H-purine | [CAS]
23599-75-9 | [Synonyms]
Racemic dihydrozeatin
(14894-18-9) dl-dihydrozeatin
DL-Dihydrozeatin >=98.0% (HPLC)
Zeatin Impurity 1(Dihydrozeatin)
6-(4-Hydroxy-3-methylbutylamino)purine
DL-Dihydrozeatin(RaceMic dihydrozeatin)
2-Methyl-4-(1H-purin-6-ylamino)-1-butanol
2-Methyl-4-(9H-purin-6-ylamino)-1-butanol
6-(4-Hydroxy-3-methylbutylamino)-9H-purine
1-Butanol, 2-methyl-4-(9H-purin-6-ylamino)- | [Molecular Formula]
C10H15N5O | [MDL Number]
MFCD00056912 | [MOL File]
23599-75-9.mol | [Molecular Weight]
221.26 |
| Chemical Properties | Back Directory | [Boiling point ]
376.5±52.0 °C(Predicted) | [density ]
1.41 | [storage temp. ]
2-8°C | [form ]
Solid | [pka]
14.99±0.10(Predicted) | [color ]
White to off-white | [BRN ]
1215977 | [InChI]
1S/C10H15N5O/c1-7(4-16)2-3-11-9-8-10(13-5-12-8)15-6-14-9/h5-7,16H,2-4H2,1H3,(H2,11,12,13,14,15) | [InChIKey]
XXFACTAYGKKOQB-UHFFFAOYSA-N | [SMILES]
CC(CO)CCNc1ncnc2nc[nH]c12 || CC(CO)CCNc1ncnc2nc[nH]c12 |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS07 | [Signal word ]
Warning | [Hazard statements ]
H317 | [Precautionary statements ]
P280 | [Hazard Codes ]
Xi | [Risk Statements ]
43 | [Safety Statements ]
36/37 | [WGK Germany ]
3 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Skin Sens. 1 |
| Hazard Information | Back Directory | [Uses]
(±)-Dihydrozeatin can be used for biological studies of the abundance of cytokinin during cytokinin metabolism, interconversion and formation of new trans-zetin metabolites[1]. | [Definition]
ChEBI: A 6-alkylaminopurine that is 7H-purin-6-amine where one of the hydrogens of the amino group is replaced by a 4-hydroxy-3-methylbutyl group. It is an intermediate in the zeatin biosynthesis. | [References]
[1] Ai LF, et al. Simple and rapid determination of N(6)-(Δ(2)-isopentenyl)adenine, zeatin, and dihydrozeatin in plants using on-line cleanup liquid chromatography coupled with hybrid quadrupole-Orbitrap high-resolution mass spectrometry. J Sep Sci. 2015 Jun;38(11):1858-65. DOI:10.1002/jssc.201401321 |
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