D-α-Tocopherol succinate - semisynthetic, 1210 IU/g , CAS No.4345-03-3

CAS: 4345-03-3 Cat. No.: D432721 Formula: C₃₃H₅₄O₅ Peso molecolare: 530.78 Beilstein Registry Number: 4038233 Numero EC: 224-403-8

QUALITÀ & PUREZZA semisynthetic, 1210 IU/g

Synonyms

DL-ALPHA-TOCOPHEROLHYDROGENSUCCINATE | DTXCID706151 | HY-131553 | 2,5,7,8-Tetramethyl-2-(4,8,12-trimethyltridecyl)-6-chromanyl hydrogen succinate, (+)- | Succinic acid, mono(2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-6-chromanyl) ester, (+)- | CCG-2

Storage

Room temperature

Shipped In

Normal

Panoramica

α-Tocopherol succinate is a fat soluble vitamin. α-Tocopherol is a form of vitamin E, which can be obtained through dietary sources. RRR-α-tocopherol is a natural form of α-Tocopherol.

Application

D-α-Tocopherol succinate has been used: to as a dietary supplement to study its immunomodulatory effects in chicks as a dietary supplement in pregnant women to evaluate its effects on arsenic exposure as an antioxidant to investigate concurrent pathways of cell death due to acute exercise

Specifiche

Sinonimi

DL-ALPHA-TOCOPHEROLHYDROGENSUCCINATE | DTXCID706151 | HY-131553 | 2,5,7,8-Tetramethyl-2-(4,8,12-trimethyltridecyl)-6-chromanyl hydrogen succinate, (+)- | Succinic acid, mono(2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-6-chromanyl) ester, (+)- | CCG-2

Specifiche e purezza

semisynthetic, 1210 IU/g

Meccanismi biochimici e fisiologici

Tocopherols (TCP) (vitamin E) are a series (α, β, γ and δ) of chiral organic molecules that vary in their degree of methylation of the phenol moiety of the chromanol ring. Tocopherols are lipid soluble anti-oxidants that protect cell membranes from oxida

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

Normal

Nomi e identificatori

Pubchem Sid

488182617

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488182617

Sorrisi canonici

CC1=C(C(=C(C2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)C)OC(=O)CCC(=O)O)C

IUPAC Name

4-oxo-4-[[(2R)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-3,4-dihydrochromen-6-yl]oxy]butanoic acid

InChIKey

IELOKBJPULMYRW-NJQVLOCASA-N

INCHI

1S/C33H54O5/c1-22(2)12-9-13-23(3)14-10-15-24(4)16-11-20-33(8)21-19-28-27(7)31(25(5)26(6)32(28)38-33)37-30(36)18-17-29(34)35/h22-24H,9-21H2,1-8H3,(H,34,35)/t23-,24-,33-/m1/s1

Isomeri SMILES

CC1=C(C(=C(C2=C1O[C@](CC2)(C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)C)OC(=O)CCC(=O)O)C

WGK Germania

1

RTECS

EJ9984000

Peso molecolare

530.78

Beilstein

4038233

Reaxy-Rn

1412198

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1412198&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Classe Prenol lipids
      • Subclass Quinone and hydroquinone lipids

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Classe: Prenol lipids
• Subclass: Quinone and hydroquinone lipids
• Intermediate Tree Nodes: Not available
• Direct Parent: Vitamin E compounds
• Alternative Parents: Diterpenoids 1-benzopyrans Fatty acid esters Alkyl aryl ethers Dicarboxylic acids and derivatives Benzenoids Carboxylic acid esters Oxacyclic compounds Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Diterpenoid - Chromane - Benzopyran - 1-benzopyran - Alkyl aryl ether - Fatty acid ester - Fatty acyl - Dicarboxylic acid or derivatives - Benzenoid - Carboxylic acid ester - Carboxylic acid derivative - Oxacycle - Carboxylic acid - Organoheterocyclic compound - Ether - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aromatic heteropolycyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as vitamin e compounds. These are a group of fat-soluble compounds containing or derived either from a tocopherol or a tocotrienol skeleton.
• External Descriptors: Not available

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

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Meccanismi d'azione

Proprietà chimiche e fisiche

• Rotazione specifica [α]: 4° (C=8,EtOH)
• Punto di fusione (°C): 75 °C
• Peso molecolare: 530.800 g/mol
• XLogP3: 10.200
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 17
• Exact Mass: 530.397 Da
• Monoisotopic Mass: 530.397 Da
• Topological Polar Surface Area: 72.800 Ų
• Heavy Atom Count: 38
• Formal Charge: 0
• Complexity: 720.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 3
• 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