Zeatin - ≥98% , CAS No.13114-27-7

CAS: 13114-27-7 Cat. No.: Z276091 Molecular Weight: 219.24

GRADE & PURITY ≥98%

Synonyms

2-methyl-4-(1h-purine-6-ylamino)-2-buten-1-ol | Z0012 | 2-Buten-1-ol, 2-methyl-4-(1H-purin-6-ylamino)- | DTXSID10859662 | E80788 | 2-methyl-4-(7H-purin-6-ylamino)but-2-en-1-ol | (E)-4-(9H-purin-6-ylamino)-2-methylbut-2-en-1-ol | 2-Methyl-4-(9H-purin-6-yla

Storage

Store at -20°C,Desiccated

Shipped In

Ice chest + Ice pads

Overview

Zeatin is a coconut milk-derived plant hormone and is a common plant cytokinin that is found in the developing or meristematic tissues and organs such as roots, shoot apex, immature organs, and others. Its structure includes the amino group of adenine being linked with the hydroxylated isoprene residue in the trans-position.

Specifications

Synonyms

2-methyl-4-(1h-purine-6-ylamino)-2-buten-1-ol | Z0012 | 2-Buten-1-ol, 2-methyl-4-(1H-purin-6-ylamino)- | DTXSID10859662 | E80788 | 2-methyl-4-(7H-purin-6-ylamino)but-2-en-1-ol | (E)-4-(9H-purin-6-ylamino)-2-methylbut-2-en-1-ol | 2-Methyl-4-(9H-purin-6-yla

Specifications & Purity

≥98%

Biochemical and Physiological Mechanisms

Coconut milk-derived plant hormone (cytokinin) that promotes growth of lateral buds, stimulates cell division (Lateral Dominance), callus initiation and seed germination.

Storage

Store at -20°C, Desiccated

Shipped In

Ice chest + Ice pads

This product requires cold chain shipping. Ground and other economy services are not available.

Note

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 504752662
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504752662
• Canonical Smiles: CC(=CCNC1=NC=NC2=C1NC=N2)CO
• IUPAC Name: 2-methyl-4-(7H-purin-6-ylamino)but-2-en-1-ol
• InChIKey: UZKQTCBAMSWPJD-UHFFFAOYSA-N
• INCHI: 1S/C10H13N5O/c1-7(4-16)2-3-11-9-8-10(13-5-12-8)15-6-14-9/h2,5-6,16H,3-4H2,1H3,(H2,11,12,13,14,15)
• Isomeric SMILES: CC(=CCNC1=NC=NC2=C1NC=N2)CO
• Molecular Weight: 219.24
• Reaxy-Rn: 18499478
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=18499478&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Class Imidazopyrimidines
      • Subclass Purines and purine derivatives
        • Level5 6-aminopurines
          • Level6 6-alkylaminopurines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Class: Imidazopyrimidines
• Subclass: Purines and purine derivatives
• Intermediate Tree Nodes: 6-aminopurines
• Direct Parent: 6-alkylaminopurines
• Alternative Parents: Secondary alkylarylamines Aminopyrimidines and derivatives Imidolactams Imidazoles Heteroaromatic compounds Azacyclic compounds Primary alcohols Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: 6-alkylaminopurine - Aminopyrimidine - Secondary aliphatic/aromatic amine - Pyrimidine - Imidolactam - Azole - Imidazole - Heteroaromatic compound - Secondary amine - Azacycle - Organopnictogen compound - Organic oxygen compound - Primary alcohol - Organooxygen compound - Organonitrogen compound - Amine - Alcohol - Hydrocarbon derivative - Organic nitrogen compound - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as 6-alkylaminopurines. These are compounds that contain an alkylamine group attached at the 6-position of a purine. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring.
• External Descriptors: a secondary metabolite

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Solubility: Soluble in sodium hydroxide；Soluble in DMSO
• Molecular Weight: 219.240 g/mol
• XLogP3: 0.700
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• Exact Mass: 219.112 Da
• Monoisotopic Mass: 219.112 Da
• Topological Polar Surface Area: 86.700 Ų
• Heavy Atom Count: 16
• Formal Charge: 0
• Complexity: 258.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 1
• The total count of all stereochemical bonds: 1
• Covalently-Bonded Unit Count: 1

References

1. Ziying Jiang, Tongrui Liu, Qi Zhang, Lili Dong, Xinyi Deng.  (2023)  PhNAL1 Is Involved in Regulating Branch Development of Petunia.  JOURNAL OF THE AMERICAN SOCIETY FOR HORTICULTURAL SCIENCE,  148  (6): (276-282).  [PMID:] [10.21273/JASHS05331-23]

2. Xinyi Zhang, Jiakun Zhou, Zemin Li, Yimin Qin, Ruitao Yu, Huaiwei Zhang, Yuhong Zheng, Jiangwei Zhu, Demeng Zhang, Li Fu.  (2023)  The Qualitative Electrochemical Determination of Multiple Components in Seaweed Fertilizer.  International Journal of Electrochemical Science,      [PMID:] [10.20964/2019.07.16]

3. Yunlei Zhou, Huanshun Yin, Yue Wang, Chengji Sui, Minghui Wang, Shiyun Ai.  (2018)  Electrochemical aptasensors for zeatin detection based on MoS2 nanosheets and enzymatic signal amplification.  ANALYST,  143  (21): (5185-5190).  [PMID:30264075] [10.1039/C8AN01356J]