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Vitamin E acetate - analytical standard, high purity , CAS No.7695-91-2
Basic Description
Synonyms
DL-alpha-Tocopherol acetate | 7695-91-2 | alpha-tochopheryl acetate | Tocopheryl acetate | all-rac-alpha-Tocopheryl acetate | E-vicotrat | 52225-20-4 | DL-alpha tocopheryl acetate | Syntopherol acetate | 2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman-6-yl acetate |
Specifications & Purity
analytical standard
Storage Temp
Store at 2-8°C,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Grade
analytical standard
Product Description
(±)-α-Tocopherol acetate (Standard) is the analytical standard of (±)-α-Tocopherol acetate. This product is intended for research and analytical applications. (±)-α-Tocopherol acetate ((±)-Vitamin E acetate), is a orally active synthetic form of vitamin E. (±)-α-Tocopherol acetate is the ester of acetic acid and α-tocopherol. (±)-α-Tocopherol acetate can be used for the research of the susceptibility of farmed fish to infectious diseases.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Lipids and lipid-like molecules
Class
Prenol lipids
Subclass
Quinone and hydroquinone lipids
Intermediate Tree Nodes
Not available
Direct Parent
Vitamin E compounds
Alternative Parents
Diterpenoids 1-benzopyrans Alkyl aryl ethers Benzenoids Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Diterpenoid - Chromane - Benzopyran - 1-benzopyran - Alkyl aryl ether - Benzenoid - Carboxylic acid ester - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Ether - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - Organooxygen compound - Aromatic heteropolycyclic compound
Description
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.
Associated Targets(Human)
Associated Targets(non-human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
IUPAC Name
[2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-3,4-dihydrochromen-6-yl] acetate
INCHI
InChI=1S/C31H52O3/c1-21(2)13-10-14-22(3)15-11-16-23(4)17-12-19-31(9)20-18-28-26(7)29(33-27(8)32)24(5)25(6)30(28)34-31/h21-23H,10-20H2,1-9H3
InChIKey
ZAKOWWREFLAJOT-UHFFFAOYSA-N
Smiles
CC1=C(C(=C(C2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)C)OC(=O)C)C
Isomeric SMILES
CC1=C(C(=C(C2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)C)OC(=O)C)C
RTECS
GA8747000
Molecular Weight
472.74
Beilstein
97512
Reaxy-Rn
455066
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=455066&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Sensitivity
Air sensitive
Refractive Index
1.497
Flash Point(°F)
437 °F
Flash Point(°C)
113 °C
Boil Point(°C)
224°C
Molecular Weight
472.700 g/mol
XLogP3
10.800
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
3
Rotatable Bond Count
14
Exact Mass
472.392 Da
Monoisotopic Mass
472.392 Da
Topological Polar Surface Area
35.500 Ų
Heavy Atom Count
34
Formal Charge
0
Complexity
601.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
3
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
Citations of This Product
1.
Wenxuan Cao, Jingbao Chen, Long Wu, Yu hang Xu, Yun Meng, Xiang Li, Zhiyun Zheng, Xiaoqin Chu.
(2023)
A Novel Molecular Reservoir Based on Reverse Self-Assembled Liquid Crystals - A New Strategy for Prolonging the Duration in Action of Analgesics. JOURNAL OF PHARMACEUTICAL SCIENCES,
112
(1985).
2.
Dan Ye, Liyan Shen, Ying Sun, Di Zhang, Xiao Tan, Panpan Jing, Min Zhang, Qingping Tian.
(2021)
Formulation and evaluation of a α-linolenic acid and vitamin E succinate microemulsion with low surfactant content and free of co-surfactant for use as a nutritional supplement. FOOD CHEMISTRY,
364
(130433).
3.
Aimin Chen, Xiao Peng, Zaifa Pan, Kang Shao, Jing Wang, Maohong Fan.
(2018)
Visual Assay of Glutathione in Vegetables and Fruits Using Quantum Dot Ratiometric Hybrid Probes. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,
66
(25):
(6431–6438).
4.
Wang Jing, Peng Xiao, Li Daquan, Jiang Xiaochun, Pan Zaifa, Chen Aimin, Huang Liang, Hu Jun.
(2018)
Ratiometric ultrasensitive fluorometric detection of ascorbic acid using a dually emitting CdSe@SiO2@CdTe quantum dot hybrid. MICROCHIMICA ACTA,
185
(1):
(1-8).
5.
Mingzhe Li, Yuyang Zhou, Hua Zhou, Dingqiang Lu.
(2025)
Catalytic synthesis of vitamin E acetate using metal organic framework material ZIF-8. JOURNAL OF COORDINATION CHEMISTRY,
6.
Wanling Chen, Nanxi Xiang, Jiahong Huang, Huixian Xu, Zhenyuan Wang, Bo Ruan, Jichuan Zhang, Chengyu Wu, Jiaheng Zhang, YanZhen Liang.
(2024)
Supramolecular collagen nanoparticles for anti-wrinkle, skin whitening, and moisturizing effects. COLLOIDS AND SURFACES B-BIOINTERFACES,
(114275).
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6 Citations
J2318813