Betanin

You don't need to be Editor-In-Chief to add or edit content to WikiDoc. You can begin to add to or edit text on this WikiDoc page by clicking on the edit button at the top of this page. Next enter or edit the information that you would like to appear here. Once you are done editing, scroll down and click the Save page button at the bottom of the page.

Betanin
Image:Betanin.png
Systematic name	2,6-Pyridinedicarboxylic acid, 4-(2-(2-carboxy-5-(beta- D-glucopyranosyloxy)- 2,3-dihydro-6- hydroxy-1H-indol -1-yl)ethenyl)- 2,3-dihydro-, (S-(R*,R*))-
Chemical formula	C24H27N2O13
Molecular mass	167.12 g/mol
Density	x.xxx g/cm³
Melting point	xx.x °C
Boiling point	xx.x °C
CAS number	7659-95-2
SMILES	OCC1[C@@H](O) [C@@H](O)[C@H] (O)[C@@H](OC2=C(O) C=C (/[N+]([C@@H] ([C@]([O-])=O) C4)=C/C=C3\C [C@H]([C@] (O)=O) NC(C(O)=O) =C3 )C4=C2)O1
Disclaimer and references

Betanin, or Beetroot Red, is a red glycosidic food dye obtained from beets; its glycone, obtained by hydrolyzing away the glucose molecule, is betanidin. As a food additive, its E number is E162. Betanin degrades when subjected to light, heat, and oxygen; therefore, it is used in frozen products, products with short shelf life, or products sold in dry state. [1] Betanin can survive pasteurization when in products with high sugar content. Its sensitivity to oxygen is highest in products with high content of water and/or containing metal cations (eg. iron and copper); antioxidants like ascorbic acid and sequestrants can slow this process down, together with suitable packaging. In dry form betanin is stable in presence of oxygen.

Betanin is usually obtained from the extract of beet juice; the concentration of betanin in red beet can reach 300-600 mg/kg. Other dietary sources of betanin and other betalains include the opuntia cactus, Swiss chard, and the leaves of some strains of amaranth.

The color of betanin depends on pH; between four and five it is bright bluish-red, becoming blue-violet as the pH increases. Once the pH reaches alkaline levels betanin hydrolyzes to a yellow-brown color.

Betanin can be also used for coloring meat and sausages.[2]

The most common uses of betanin are in coloring ice cream and powdered soft drink beverages; other uses are in some sugar confectionery, e.g. fondants, sugar strands, sugar coatings, and fruit or cream fillings. In hot processed candies, it can be used if added at the final part of the processing. Betanin is also used in soups as well as tomato and bacon products.

Betanin absorbs well from the gut and acts as an antioxidant.

Betanin is a betalain pigment, together with isobetanin, probetanin, and neobetanin. Other pigments contained in beet are indicaxanthin and vulgaxanthins.

See also

• Betalain

v • d • e Major families of biochemicals
Peptides | Amino acids | Nucleic acids | Carbohydrates | Nucleotide sugars | Lipids | Terpenes | Carotenoids | Tetrapyrroles | Enzyme cofactors | Steroids | Flavonoids | Alkaloids | Polyketides | Glycosides
Analogues of nucleic acids:	Types of Glycosides	Analogues of nucleic acids:
Bond:	O-glycosidic bond | S-glycosidic bond | N-glycosidic bond
Geometry:	α-Glycoside | β-Glycoside | 1,4-Glycoside | 1,6-Glycoside
Glycone:	Glucoside | Fructoside | Glucuronide
Aglycone:	Alcoholic glycoside | Anthraquinone glycoside | Coumarin glycoside | Cyanogenic glycoside | Flavonoid glycoside | Phenolic glycoside | Saponin | Cardiac glycoside | Steviol glycoside | Thioglycoside | Glycosylamine | Bufanolide | Cardenolide

de:Betanin nl:Betanine