Retinol - BioReagent, ≥97,5%(HPLC), ~3100 U/mg , CAS No.68-26-8

CAS: 68-26-8 Cat. No.: R755730 Fórmula: C₂₀H₃₀O Peso molecular: 286.45 Beilstein Registry Number: 403040 Número EC: 200-683-7

CALIDAD & PUREZA BioReagent, ≥97.5%(HPLC), ~3100 U/mg

Storage

Protegido de la luz,Almacenar a -20°C,Cargado con argón

Shipped In

Hielera + almohadillas de hielo

Descripción general

El retinol o alcohol de vitamina A es la principal forma circulante de vitamina A

Especificaciones

Especificaciones y pureza

BioReagent, ≥97,5%(HPLC), ~3100 U/mg

Mecanismos bioquímicos y fisiológicos

No es biológicamente activo y funciona como precursor de los retinoides activos. El retinol se convierte en retinaldehído y posteriormente en ácido retinoico.Retinal, retinol y ácido retinoico son las formas aldehído, alcohol y ácido de la vitamina A. Los

Condiciones de almacenamiento de almacenamiento

Protegido de la luz,Almacenar a -20°C,Cargado con argón

Enviado en

Hielera + almohadillas de hielo

Grado

BioReagent

Pureza

≥97.5%(HPLC)

Nombres e identificadores

Pubchem Sid

528775693

Sonrisas canónicas

CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CCO)C)C

IUPAC Name

(2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohexen-1-yl)nona-2,4,6,8-tetraen-1-ol

InChIKey

FPIPGXGPPPQFEQ-OVSJKPMPSA-N

INCHI

1S/C20H30O/c1-16(8-6-9-17(2)13-15-21)11-12-19-18(3)10-7-14-20(19,4)5/h6,8-9,11-13,21H,7,10,14-15H2,1-5H3/b9-6+,12-11+,16-8+,17-13+

Isómeros SMILES

CC1=C(C(CCC1)(C)C)/C=C/C(=C/C=C/C(=C/CO)/C)/C

WGK Alemania

3

RTECS

VH6750000

Peso molecular

286.45

Beilstein

403040

Reaxy-Rn

1913942

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1913942&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Clase Prenol lipids
      • Subclass Retinoids

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Clase: Prenol lipids
• Subclass: Retinoids
• Intermediate Tree Nodes: Not available
• Direct Parent: Retinoids
• Alternative Parents: Diterpenoids Fatty alcohols Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic homomonocyclic compounds
• Substituents: Retinoid skeleton - Diterpenoid - Fatty alcohol - Fatty acyl - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as retinoids. These are oxygenated derivatives of 3,7-dimethyl-1-(2,6,6-trimethylcyclohex-1-enyl)nona-1,3,5,7-tetraene and derivatives thereof.
• External Descriptors: Retinoids

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

Propiedades químicas y físicas

• Sensibilidad: Hygroscopic
• Índice de refracción: 1.641
• Punto de ebullición (°C): 120-125°C
• Punto de fusión (°C): 61-63°C
• Peso molecular: 286.500 g/mol
• XLogP3: 5.700
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 5
• Exact Mass: 286.23 Da
• Monoisotopic Mass: 286.23 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 21
• Formal Charge: 0
• Complexity: 496.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 4
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 4
• Covalently-Bonded Unit Count: 1