Relevant Data

Food Additives Approved by European Union:


General Information

Synonyms: VITAMIN E CONCENTRATE
Chemical Names: MIXED TOCOPHEROL CONCENTRATE CONTAINS TOCOPHEROLS SUCH AS d-alpha-, d-beta-, d-gamma-, d-delta-TOCOPHEROLS
CAS number: 59-02-9 (VITAMIN E)
INS:

307b

Functional Class: Food Additives
ANTIOXIDANT

From apps.who.int


Evaluations

From apps.who.int



GSFA Provisions for TOCOPHEROL CONCENTRATE, MIXED

Number Food Category Max Level Notes
01.3.2

Beverage whiteners

200 mg/kg Note XS250,Note XS252
02.1.1

Butter oil, anhydrous milkfat, ghee

500 mg/kg Note 171
07.2.1

Cakes, cookies and pies (e.g. fruit-filled or custard types)

200 mg/kg Note 389
06.5

Cereal and starch based desserts (e.g. rice pudding, tapioca pudding)

500 mg/kg Note 15
05.1.4

Cocoa and chocolate products

750 mg/kg Note 15,Note 168
05.1.2

Cocoa mixes (syrups)

500 mg/kg Note 15
05.1.3

Cocoa-based spreads, including fillings

100 mg/kg Note XS86,Note 15
05.2

Confectionery including hard and soft candy, nougats, etc. other than food categories 05.1, 05.3 and 05.4

500 mg/kg Note XS309R,Note 15
01.7

Dairy-based desserts (e.g. pudding, fruit or flavoured yoghurt)

500 mg/kg Note XS243
05.4

Decorations (e.g. for fine bakery wares), toppings (non-fruit) and sweet sauces

500 mg/kg Note 15
06.4.2

Dried pastas and noodles and like products

500 mg/kg Note 211
04.2.2.2

Dried vegetables (including mushrooms and fungi, roots and tubers, pulses and legumes, and aloe vera), seaweeds, and nuts and seeds

200 mg/kg Note XS38
08.4

Edible casings (e.g. sausage casings)

5,000 mg/kg Note 365
03.0

Edible ices, including sherbet and sorbet

500 mg/kg Note 15
01.1.4

Flavoured fluid milk drinks

200 mg/kg Note 15
06.2.1

Flours

5,000 mg/kg Note 186,Note 15
08.1.2

Fresh meat, poultry, and game, comminuted

300 mg/kg Note 15,Note 281
04.1.2.8

Fruit preparations, including pulp, purees, fruit toppings and coconut milk

150 mg/kg Note XS240,Note XS314R
04.1.2.9

Fruit-based desserts, including fruit-flavoured water-based desserts

500 mg/kg Note 15
05.1.5

Imitation chocolate, chocolate substitute products

500 mg/kg Note 15
02.1.3

Lard, tallow, fish oil, and other animal fats

300 mg/kg Note 358
07.2.3

Mixes for fine bakery wares (e.g. cakes, pancakes)

200 mg/kg Note 11
06.4.3

Pre-cooked pastas and noodles and like products

200 mg/kg Note 211
08.3

Processed comminuted meat, poultry, and game products

500 mg/kg Note XS98,Note XS89,Note XS88
08.2

Processed meat, poultry, and game products in whole pieces or cuts

500 mg/kg Note XS97,Note XS96
12.5

Soups and broths

50 mg/kg Note 346
01.6.1

Unripened cheese

200 mg/kg Note 168,Note 351
04.2.2.5

Vegetable (including mushrooms and fungi, roots and tubers, pulses and legumes, and aloe vera), seaweed, and nut and seed purees and spreads (e.g., peanut butter)

300 mg/kg Note XS57
02.1.2

Vegetable oils and fats

300 mg/kg Note 356,Note 357

From www.fao.org


Computed Descriptors

Download SDF
2D Structure
CID14985
IUPAC Name(2R)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-3,4-dihydrochromen-6-ol
InChIInChI=1S/C29H50O2/c1-20(2)12-9-13-21(3)14-10-15-22(4)16-11-18-29(8)19-17-26-25(7)27(30)23(5)24(6)28(26)31-29/h20-22,30H,9-19H2,1-8H3/t21-,22-,29-/m1/s1
InChI KeyGVJHHUAWPYXKBD-IEOSBIPESA-N
Canonical SMILESCC1=C(C(=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)C)O
Molecular FormulaC29H50O2
Wikipediavitamin E

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight430.717
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count12
Complexity503.0
CACTVS Substructure Key Fingerprint A A A D c f B 4 M A A A A A A A A A A A A A A A A A A A A A A A A A A 0 Q A A A A A A A A A C R A A A A G g A A C A A A D U S A m A A C B o A A B g C A A g B A A A A C C A A g I A A A i A A E C I g M J i K G M B q C e C C k w B E I u A f A w P A O w Q A D A A A Y A A C C A A Y A A D A A A A A A A A A A A A = =
Topological Polar Surface Area29.5
Monoisotopic Mass430.381
Exact Mass430.381
XLogP3None
XLogP3-AA10.7
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count31
Defined Atom Stereocenter Count3
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Isotope Atom Count0
Covalently-Bonded Unit Count1

From Pubchem


Food Additives Biosynthesis/Degradation


ADMET Predicted Profile --- Classification

Model Result Probability
Absorption
Blood-Brain BarrierBBB+0.9767
Human Intestinal AbsorptionHIA+0.9795
Caco-2 PermeabilityCaco2+0.8484
P-glycoprotein SubstrateSubstrate0.7189
P-glycoprotein InhibitorNon-inhibitor0.7598
Inhibitor0.7802
Renal Organic Cation TransporterNon-inhibitor0.7882
Distribution
Subcellular localizationMitochondria0.7187
Metabolism
CYP450 2C9 SubstrateNon-substrate0.6949
CYP450 2D6 SubstrateNon-substrate0.7813
CYP450 3A4 SubstrateSubstrate0.7533
CYP450 1A2 InhibitorNon-inhibitor0.8122
CYP450 2C9 InhibitorNon-inhibitor0.9071
CYP450 2D6 InhibitorNon-inhibitor0.9231
CYP450 2C19 InhibitorNon-inhibitor0.9026
CYP450 3A4 InhibitorNon-inhibitor0.8309
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.7762
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.7192
Non-inhibitor0.6449
AMES ToxicityNon AMES toxic0.9132
CarcinogensNon-carcinogens0.8813
Fish ToxicityHigh FHMT0.9394
Tetrahymena Pyriformis ToxicityHigh TPT0.9960
Honey Bee ToxicityHigh HBT0.7221
BiodegradationNot ready biodegradable0.9965
Acute Oral ToxicityIII0.7164
Carcinogenicity (Three-class)Non-required0.7474

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-4.5216LogS
Caco-2 Permeability1.6020LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity2.1598LD50, mol/kg
Fish Toxicity0.0264pLC50, mg/L
Tetrahymena Pyriformis Toxicity2.0192pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassLipids and lipid-like molecules
ClassPrenol lipids
SubclassQuinone and hydroquinone lipids
Intermediate Tree NodesVitamin E compounds
Direct ParentTocopherols
Alternative Parents
Molecular FrameworkAromatic heteropolycyclic compounds
SubstituentsTocopherol - Diterpenoid - 1-benzopyran - Benzopyran - Chromane - Alkyl aryl ether - Benzenoid - Oxacycle - Organoheterocyclic compound - Ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as tocopherols. These are vitamin E derivatives containing a saturated trimethyltridecyl chain attached to the carbon C6 atom of a benzopyran ring system. The differ from tocotrienols that contain an unsaturated trimethyltrideca-3,7,11-trien-1-yl chain.

From ClassyFire