1-Triacontanol - ≥85% , CAS No.593-50-0

CAS: 593-50-0 Cat. No.: T113181 Peso molecular: 438.81 Beilstein Registry Number: 1711965 Número EC: 209-794-5 PubChem CID: 68972

GRADE & PURITY ≥85%

Synonyms

1-?Triacontanol | Melissyl alcohol | Myricyl alcohol | FT-0608318 | NSC402492 | NSC-402492 | Q4860821 | Well-Bloom | DTXSID5029188 | TRICONTANOL (CONSTITUENT OF SAW PALMETTO) | TRICONTANOL (CONSTITUENT OF SAW PALMETTO) [DSC] | ULTRIA | A832277 | SR-010009

Storage

Room temperature

Shipped In

Normal

Descripción general

n-Triacontanol is a plant growth regulator found in the plant cuticle waxes and in beeswax as the palmitate ester. Has been reported to have growth enhancing properties when applied to the leaves of growing plants.
A plant growth regulator

Specifications

Sinónimos

1-?Triacontanol | Melissyl alcohol | Myricyl alcohol | FT-0608318 | NSC402492 | NSC-402492 | Q4860821 | Well-Bloom | DTXSID5029188 | TRICONTANOL (CONSTITUENT OF SAW PALMETTO) | TRICONTANOL (CONSTITUENT OF SAW PALMETTO) [DSC] | ULTRIA | A832277 | SR-010009

Especificaciones y pureza

≥85%

Mecanismos bioquímicos y fisiológicos

Naturally occurring plant-growth regulator. Present in plant cuticle waxes and in beeswax as the palmitate.

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Nota

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.

Pureza

≥85%

Nombres e identificadores

• Pubchem Sid: 504754315
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504754315
• Sonrisas canónicas: CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO
• IUPAC Name: triacontan-1-ol
• InChIKey: REZQBEBOWJAQKS-UHFFFAOYSA-N
• INCHI: 1S/C30H62O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-30-31/h31H,2-30H2,1H3
• Isómeros SMILES: CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO
• PubChem CID: 68972
• Peso molecular: 438.81
• Beilstein: 1711965

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Clase Fatty Acyls
      • Subclass Fatty alcohols

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Clase: Fatty Acyls
• Subclass: Fatty alcohols
• Intermediate Tree Nodes: Not available
• Direct Parent: Fatty alcohols
• Alternative Parents: Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Fatty alcohol - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms.
• External Descriptors: a long-chain alcohol - a primary alcohol - a fatty alcohol

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

Objetivos asociados (no humanos)

Ptpn1 Protein-tyrosine phosphatase 1B (270 Activities)

Discover Target: Ptpn1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Human immunodeficiency virus 1 (70413 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in ethanol (sparingly), DMSO (sparingly), DMF (sparingly), and chloroform (~1.7 mg/ml). Insoluble in water.
• Índice de refracción: 1.46
• Punto de ebullición (°C): 443.3° C
• Punto de fusión (°C): 86.5-87.5°C
• Peso molecular: 438.800 g/mol
• XLogP3: 14.900
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 28
• Exact Mass: 438.48 Da
• Monoisotopic Mass: 438.48 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 31
• Formal Charge: 0
• Complexity: 288.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Feng Du, Mengyu Wang, Libin Wang, Yushan Li, Yuangao Wang, Wenan Deng, Wenjuan Yan, Xin Jin.  (2023)  Catalytic conversion of polyoxymethylene with bio-derived substrates: kinetic modeling on solvent enhancement effect and experimental studies on reaction mechanism.  CHEMICAL ENGINEERING SCIENCE,      [PMID:] [10.1016/j.ces.2023.118670]

2. Xiyang Wang, Siraj Ullah, Shuozhen Hu, Xinsheng Zhang.  (2022)  Investigation and Separation of Chromogenic Substances in Glyoxylic Acid Generated by Electrochemical Reduction of Oxalic Acid.  ChemistrySelect,  7  (27): (e202201140).  [PMID:] [10.1002/slct.202201140]

3. Guojun Liu, Shaoshuai Wang, Caiming Zhou, Qiang Zhao, Jiaxue Hu, Zhenzheng Gui, Yuhui Chen, Yong Huang, Peng Zhang, Fenfen Wang.  (2024)  Boosting the activity of BiVOx via vanadium-promotion for highly selective oxidation of biomass-derived xylose toward formic acid.  FUEL,      [PMID:] [10.1016/j.fuel.2024.132420]