Information about Xylitol
| Xylitol[1] | |
|---|---|
![]() | |
| IUPAC name | (2S,3R,4R)-Pentane-1,2,3,4,5-pentanol |
| Other names | 1,2,3,4,5-Pentahydroxypentane |
| Identifiers | |
| CAS number | |
| Properties | |
| Molecular formula | C5H12O5 |
| Molar mass | 152.15 g/mol |
| Density | 1.52 g/cm³ |
| Melting point | 92-96 °C |
| Boiling point | 216 °C |
| Related Compounds | |
| Related alkanes | Pentane |
| Except where noted otherwise, data are given for materials in their standard state (at 25 C, 100 kPa) | |
Xylitol, also called wood sugar or birch sugar, is a five-carbon sugar alcohol that is used as a sugar substitute. Xylitol is a naturally occurring sweetener found in the fibers of many fruits and vegetables, including various berries, corn husks, oats, and mushrooms.[2] It can be extracted from corn fiber,[3] birch, raspberries, plums, and corn. Xylitol is roughly as sweet as sucrose but with two-thirds the food energy.
Extraction of xylitol
Xylitol was first derived from Birch trees in Finland in the 19th century and was first popularized in Europe as a safe sweetener for diabetics that would not impact insulin levels. In the late 20th century, xylitol in granular form began to be mass produced in the United States under the brand name "Ultimate Sweetener" using beet plants in California. Today, using maize sources, most world supplies reportedly come from China.Properties
One teaspoon of xylitol contains 9.6 calories, as compared to one teaspoon of sugar, which has 15 calories. Xylitol contains zero net effective carbohydrates, whereas sugar contains 4 grams per teaspoon. Xylitol has virtually no aftertaste, and is advertised as "safe for diabetics and individuals with hyperglycemia". This is because sugar-alcohols have less impact on a person's blood sugar than regular sugars[4].Dietary use worldwide
Xylitol is widely used in Finland, its "home country". Many Finnish confectioneries employ xylitol, or have a xylitol version available. Virtually all chewing gum sold in Finland, and in the rest of Europe, is sweetened with xylitol.The formerly Spanish company, now Italian, Chupa Chups makes a xylitol-based breath mint, Smint, that it markets worldwide.
In China, Japan, and South Korea, xylitol is found in wide assortment of chewing gums. There is brand of gum named "Xylitol" in all three countries; Japan also has a brand called "Xylish". In addition, when Extra introduced xylitol-containing products to Hong Kong and Guangdong, the word "xylitol" is transcribed into Cantonese as "晒駱駝" (Jyutping: saai3 lok6 to4), which literally means "suntan camel", and the camel is used as a figurative icon in its advertisements.[5]
In 2004, popular North American Trident gum was reformulated to include xylitol, but not as the main sweetener (which are still sorbitol and maltitol). Also sold in North America is Carefree Koolerz, which is a sugarless gum sweetened exclusively with xylitol. It is also found in Smokey Mountain Snuff,[6] and IceBreakers brand Ice Cubes Gum from Hershey.
In 2006, William Wrigley Jr. Company reformulated their Orbit gum to contain xylitol and released it under the name "Orbit Complete."
Medical applications
Dental care
Xylitol is a "toothfriendly" sugar. In addition to not encouraging tooth decay (by replacing dietary sugars), xylitol may actively aid in repairing minor cavities caused by dental caries. Recent research[7] confirms a plaque-reducing effect and suggests that the compound, having some chemical properties similar to sucrose, attracts and then "starves" harmful micro-organisms, allowing the mouth to remineralize damaged teeth with less interruption. (However, this same effect also interferes with yeast micro-organisms and others, so xylitol is inappropriate for making yeast-based bread, for instance.)Xylitol based products are allowed by the U.S. Food and Drug Administration to make the medical claim that they do not promote dental caries.[8]
A recent study demonstrated that a water additive for animals containing xylitol was effective in reducing plaque and calculus accumulation in cats.[9]
Diabetes
Possessing approximately 40% less food energy,[10] xylitol is a low-calorie alternative to table sugar. Absorbed more slowly than sugar, it doesn't contribute to high blood sugar levels or the resulting hyperglycemia caused by insufficient insulin response.Osteoporosis
Xylitol also appears to have potential as a treatment for osteoporosis. A group of Finnish researchers has found that dietary xylitol prevents weakening of bones in laboratory rats, and actually improves bone density.[11][12]Ear and upper respiratory infections
Studies have shown that xylitol chewing gum can help prevent ear infections[13] (acute otitis media); the act of chewing and swallowing assists with the disposal of earwax and clearing the middle ear, whilst the presence of xylitol prevents the growth of bacteria in the eustachian tubes which connect the nose and ear.[14] This action that xylitol has on bacteria in the back of the nose is best explained on the site dealing with the nasal application of xylitol.[15] When bacteria enter the body they hold on to the tissues by hanging on to a variety of sugar complexes. The open nature of xylitol and its ability to form many different sugar-like structures appears to interfere with the ability of many bacteria to adhere.[16] Xylitol can be applied nasally through a saline solution containing xylitol, such as Xlear Nasal Wash.Candida yeast
A recent report suggests that consumption of xylitol may help control oral infections of Candida yeast; in contrast, galactose, glucose and sucrose may increase proliferation.[17]Health concerns
Xylitol, like most sugar alcohols, can have a mild laxative effect at high doses. It has no known toxicity, and people have consumed as much as 400 grams daily for long periods with no apparent ill effects.[18]Dogs ingesting foods containing high doses of xylitol (greater than 100mg xylitol consumed per kg bodyweight) have presented with low blood sugar (hypoglycaemia) which can be life-threatening.[19] Low blood sugar can manifest as loss of coordination, depression, collapse and seizures as soon as 30 minutes after ingestion.[20][21] Intake of very high doses of xylitol (greater than 500 - 1000 mg/kg bwt) has also been implicated in liver failure in 8 dogs, which can be fatal.[22]
One reported death occurred in a standard poodle that ate five or six cookies sweetened with xylitol.[23]
As humans can tolerate much higher doses of xylitol, large amounts of xylitol can be found in even small quantities of food such as sugar-free gums, baked goods and tooth pastes.
Dogs that have eaten products containing high levels of xylitol might need immediate medical attention even if they are not yet showing illness. Sick dogs (vomiting, weak, seizuring, etc) are likely to need aggressive veterinary treatment and close monitoring of blood values.[24][25][26]
Other applications of xylitol
ASICS Corp., a Japanese company, markets a line of women’s t-shirts with xylitol infused into the fabric. Xylitol, like several other sugar alcohols, exhibits a cooling effect in the mouth. The t-shirts are intended to utilize this same property to keep a person cooler in warm weather.[27]This application has also been used by YONEX to make shirts
References
1. ^ MSDS for xylitol
2. ^ Gare, Fran (Feb 1, 2003). The Sweet Miracle of Xylitol. Basic Health Publications, Inc.. ISBN 1-59120-038-5.
3. ^ R Sreenivas Rao, Ch. Pavanajyothi, RS Prakasham, PN Sharma, L Venkateswar Rao (2006) Xylitol production from corn fiber and sugarcane bagasse hydrolysates by Candida tropicalis Bioresource Technology 97:1974-1978.
4. ^ [1]
5. ^ Xylitol advertisement in Guangdong
6. ^ Smokey Mountain Snuff FAQ
7. ^ Tanzer, JM (1995). Xylitol chewing gum and dental caries. International dental journal 45(1 Suppl 1):65-76. (online abstract)
8. ^ U.S. FDA 21 CFR §101.80
9. ^ Clarke, D.E. (2006) Drinking Water Additive Decreases Plaque and Calculus Accumulation in Cats. J Vet Dent(23)2:79-82
10. ^ www.diabetes.org.nz/food/artificialsweeteners.html
11. ^ Mattila PT, Svanberg MJ, Jämsä T, Knuuttila ML (2002). Improved bone biomechanical properties in xylitol-fed aged rats.Metabolism 51(1):92-6. (online abstract)
12. ^ Mattila, PT (1999). Dietary xylitol in the prevention of experimental osteoporosis: Beneficial effects on bone resorption, structure and biomechanics. Dissertation, Institute of Dentistry, University of Oulu. (online)
13. ^ Uhari M, et al. (1998). A novel use of xylitol sugar in preventing acute otitis media. Pediatrics, 102(4): 879–974.
14. ^ Drgreene.com
15. ^ Nasal-xylitol.com
16. ^ Besttreaments.co.uk
17. ^ Abu-Elteen, Khaled H. The influence of dietary carbohydrates on in vitro adherence of four Candida species to human buccal epithelial cells. Microbial Ecology in Health and Disease (2005), 17(3), 156-162
18. ^ [2] Mäkinen,longterm tolerance
19. ^ Dunayer, E.K., Gwaltney-Brant, S.M. (2006) Acute hepatic failure and coagulopathy associated with xylitol ingestion in eight dogs, Journal of the American Veterinary Medical Association (229)7:1113-1117
20. ^ ASPCA article
21. ^ Dunayer, E.K (2004) Hypoglycemia following canine ingestion of xylitol-containing gum, Veterinary and Human Toxicology 46(2):87-88
22. ^ Dunayer, E.K (2006) New findings on the effects of xylitol ingestion in dogs Veterinary Medicine 101(12):791-797
23. ^ Dunayer, E.K (2006) New findings on the effects of xylitol ingestion in dogs Veterinary Medicine 101(12):791-797
24. ^ Dunayer, E.K., Gwaltney-Brant, S.M. (2006) Acute hepatic failure and coagulopathy associated with xylitol ingestion in eight dogs, Journal of the American Veterinary Medical Association (229)7:1113-1117
25. ^ AVMA Press Release
26. ^ Dunayer, E.K (2006) New findings on the effects of xylitol ingestion in dogs Veterinary Medicine 101(12):791-797
27. ^ information from the Danisco website
2. ^ Gare, Fran (Feb 1, 2003). The Sweet Miracle of Xylitol. Basic Health Publications, Inc.. ISBN 1-59120-038-5.
3. ^ R Sreenivas Rao, Ch. Pavanajyothi, RS Prakasham, PN Sharma, L Venkateswar Rao (2006) Xylitol production from corn fiber and sugarcane bagasse hydrolysates by Candida tropicalis Bioresource Technology 97:1974-1978.
4. ^ [1]
5. ^ Xylitol advertisement in Guangdong
6. ^ Smokey Mountain Snuff FAQ
7. ^ Tanzer, JM (1995). Xylitol chewing gum and dental caries. International dental journal 45(1 Suppl 1):65-76. (online abstract)
8. ^ U.S. FDA 21 CFR §101.80
9. ^ Clarke, D.E. (2006) Drinking Water Additive Decreases Plaque and Calculus Accumulation in Cats. J Vet Dent(23)2:79-82
10. ^ www.diabetes.org.nz/food/artificialsweeteners.html
11. ^ Mattila PT, Svanberg MJ, Jämsä T, Knuuttila ML (2002). Improved bone biomechanical properties in xylitol-fed aged rats.Metabolism 51(1):92-6. (online abstract)
12. ^ Mattila, PT (1999). Dietary xylitol in the prevention of experimental osteoporosis: Beneficial effects on bone resorption, structure and biomechanics. Dissertation, Institute of Dentistry, University of Oulu. (online)
13. ^ Uhari M, et al. (1998). A novel use of xylitol sugar in preventing acute otitis media. Pediatrics, 102(4): 879–974.
14. ^ Drgreene.com
15. ^ Nasal-xylitol.com
16. ^ Besttreaments.co.uk
17. ^ Abu-Elteen, Khaled H. The influence of dietary carbohydrates on in vitro adherence of four Candida species to human buccal epithelial cells. Microbial Ecology in Health and Disease (2005), 17(3), 156-162
18. ^ [2] Mäkinen,longterm tolerance
19. ^ Dunayer, E.K., Gwaltney-Brant, S.M. (2006) Acute hepatic failure and coagulopathy associated with xylitol ingestion in eight dogs, Journal of the American Veterinary Medical Association (229)7:1113-1117
20. ^ ASPCA article
21. ^ Dunayer, E.K (2004) Hypoglycemia following canine ingestion of xylitol-containing gum, Veterinary and Human Toxicology 46(2):87-88
22. ^ Dunayer, E.K (2006) New findings on the effects of xylitol ingestion in dogs Veterinary Medicine 101(12):791-797
23. ^ Dunayer, E.K (2006) New findings on the effects of xylitol ingestion in dogs Veterinary Medicine 101(12):791-797
24. ^ Dunayer, E.K., Gwaltney-Brant, S.M. (2006) Acute hepatic failure and coagulopathy associated with xylitol ingestion in eight dogs, Journal of the American Veterinary Medical Association (229)7:1113-1117
25. ^ AVMA Press Release
26. ^ Dunayer, E.K (2006) New findings on the effects of xylitol ingestion in dogs Veterinary Medicine 101(12):791-797
27. ^ information from the Danisco website
See also
- Other sugar alcohols: mannitol, sorbitol, erythritol, maltitol, lactitol
- Herbal sweetener: stevia
- Artificial sweeteners: aspartame, sucralose
- Another birch-extracted treat: birch syrup
- L-xylulose reductase
E numbers |
|---|
Colours (E100–199) • Preservatives (E200–299) • Antioxidants & Acidity regulators (E300–399) • Thickeners, stabilisers & emulsifiers (E400–499) • pH regulators & anti-caking agents (E500–599) • Flavour enhancers (E600–699) • Miscellaneous (E900–999) • Additional chemicals (E1100–1599)
Waxes (E900–909) • Synthetic glazes (E910–919) • Improving agents (E920–929) • Packaging gases (E930–949) • Sweeteners (E950–969) • Foaming agents (E990–999) Acesulfame K (E950) • Aspartame (E951) • Cyclamate (E952) • Isomalt (E953) • Saccharin (E954) • Sucralose (E955) • Alitame (E956) • Thaumatin (E957) • Neohesperidin dihydrochalcone (E959) • Salt of aspartame-acesulfame (E962) • Maltitol (E965) • Lactitol (E966) • Xylitol (E967) |
IUPAC nomenclature is a system of naming chemical compounds and of describing the science of chemistry in general. It is developed and kept up to date under the auspices of the International Union of Pure and Applied Chemistry (IUPAC).
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CAS registry numbers are unique numerical identifiers for chemical compounds, polymers, biological sequences, mixtures and alloys. They are also referred to as CAS numbers, CAS RNs or CAS #s.
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A chemical formula is a concise way of expressing information about the atoms that constitute a particular chemical compound. A chemical formula is also a short way of showing how a chemical reaction occurs.
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4, 2
(mildly acidic oxide)
Electronegativity 2.55 (Pauling scale)
Ionization energies
(more) 1st: 1086.5 kJmol−1
2nd: 2352.6 kJmol−1
3rd: 4620.5 kJmol−1
Atomic radius 70 pm
Atomic radius (calc.
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(mildly acidic oxide)
Electronegativity 2.55 (Pauling scale)
Ionization energies
(more) 1st: 1086.5 kJmol−1
2nd: 2352.6 kJmol−1
3rd: 4620.5 kJmol−1
Atomic radius 70 pm
Atomic radius (calc.
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1, −1
(amphoteric oxide)
Electronegativity 2.20 (Pauling scale) More
Atomic radius 25 pm
Atomic radius (calc.) 53 pm
Covalent radius 37 pm
Van der Waals radius 120 pm
Miscellaneous
Thermal conductivity (300 K) 180.
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(amphoteric oxide)
Electronegativity 2.20 (Pauling scale) More
Atomic radius 25 pm
Atomic radius (calc.) 53 pm
Covalent radius 37 pm
Van der Waals radius 120 pm
Miscellaneous
Thermal conductivity (300 K) 180.
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2, −1
(neutral oxide)
Electronegativity 3.44 (Pauling scale)
Ionization energies
(more) 1st: 1313.9 kJmol−1
2nd: 3388.3 kJmol−1
3rd: 5300.5 kJmol−1
Atomic radius 60 pm
Atomic radius (calc.
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(neutral oxide)
Electronegativity 3.44 (Pauling scale)
Ionization energies
(more) 1st: 1313.9 kJmol−1
2nd: 3388.3 kJmol−1
3rd: 5300.5 kJmol−1
Atomic radius 60 pm
Atomic radius (calc.
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Molar mass, symbol M,[1] is the mass of one mole of a substance (chemical element or chemical compound).[2] It is a physical property which is characteristic of each pure substance.
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In physics, density is mass m per unit volume V—how heavy something is compared to its size. A small, heavy object, such as a rock or a lump of lead, is denser than a lighter object of the same size or a larger object of the same weight, such as pieces of
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boiling point of a liquid is the temperature at which the vapor pressure of the liquid equals the environmental pressure surrounding the liquid.[1][2][3][4]
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Alkanes, also known as Paraffins, are chemical compounds that consist only of the elements carbon (C) and hydrogen (H) (i.e. hydrocarbons), where each of these atoms are linked together exclusively by single bonds (i.e. they are saturated compounds) without any cyclic structure (i.
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Pentane, also known as amyl hydride or skellysolve A is an alkane hydrocarbon. It is a liquid commodity chemical compound, mainly used as fuel and as a solvent.
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standard state of a material is its state at 1 bar (100 kilopascals exactly). This pressure was changed from 1 atm (101.325 kilopascals) by IUPAC in 1990.[1] The standard state of a material can be defined at any given temperature, most commonly 25 degrees Celsius,
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A sugar alcohol (also known as a polyol, polyhydric alcohol, or polyalcohol) is a hydrogenated form of carbohydrate, whose carbonyl group (aldehyde or ketone, reducing sugar) has been reduced to a primary or secondary hydroxyl group.
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sugar substitute, or artificial sweetener, is a food additive which attempts to duplicate the effect of sugar or corn syrup in taste, but usually with less food energy.
An important class of sugar substitutes are known as high intensity sweeteners.
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An important class of sugar substitutes are known as high intensity sweeteners.
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Betula
L.
Species
Many species;
see text and classification
Birch is the name of any tree of the genus Betula (Bé-tu-la
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L.
Species
Many species;
see text and classification
Birch is the name of any tree of the genus Betula (Bé-tu-la
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The raspberry (plural, raspberries) is the edible fruit of a number of species of the genus Rubus. The name originally refers in particular to the European species Rubus idaeus
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Prunus
Species
See text.
A plum or gage is a stone fruit tree in the genus Prunus, subgenus Prunus. The subgenus is distinguished from other subgenera (peaches, cherries, bird cherries, etc) in the shoots having a terminal bud and
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Species
See text.
A plum or gage is a stone fruit tree in the genus Prunus, subgenus Prunus. The subgenus is distinguished from other subgenera (peaches, cherries, bird cherries, etc) in the shoots having a terminal bud and
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Z. mays
Binomial name
Zea mays
L.
Maize (IPA: /ˈmeɪz/) (Zea mays L. ssp.
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Binomial name
Zea mays
L.
Maize (IPA: /ˈmeɪz/) (Zea mays L. ssp.
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Sucrose (common name: table sugar, also called saccharose) is a disaccharide (glucose + fructose) with the molecular formula C12H22O11. Its systematic name is α-D-glucopyranosyl-(1→2)-β-D-fructofuranose.
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Food energy is the amount of energy in food that is available through digestion. The values for food energy are expressed in kilocalories (kcal) and kilojoules (kJ).
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Betula
L.
Species
Many species;
see text and classification
Birch is the name of any tree of the genus Betula (Bé-tu-la
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L.
Species
Many species;
see text and classification
Birch is the name of any tree of the genus Betula (Bé-tu-la
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Anthem
Maamme (Finnish)
VÃ¥rt land (Swedish)
Our Land
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Maamme (Finnish)
VÃ¥rt land (Swedish)
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Europe is one of the seven traditional continents of the Earth. Physically and geologically, Europe is the westernmost peninsula of Eurasia, west of Asia. Europe is bounded to the north by the Arctic Ocean, to the west by the Atlantic Ocean, to the south by the Mediterranean Sea,
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Diabetes mellitus
Classification & external resources
ICD-10 E 10. –E 14.
ICD-9 250
MedlinePlus 001214
eMedicine med/546 emerg/134
MeSH C18.452.394.
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Classification & external resources
ICD-10 E 10. –E 14.
ICD-9 250
MedlinePlus 001214
eMedicine med/546 emerg/134
MeSH C18.452.394.
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- ''Note: This article title may be easily confused with inulin.
Insulin is an animal hormone whose presence informs the body's cells that the animal is well fed, causing liver and muscle cells to take in glucose and store it in the form of glycogen, and
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Z. mays
Binomial name
Zea mays
L.
Maize (IPA: /ˈmeɪz/) (Zea mays L. ssp.
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Binomial name
Zea mays
L.
Maize (IPA: /ˈmeɪz/) (Zea mays L. ssp.
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A calorie is a unit of measurement for energy. Calorie is French and derives from the Latin calor (heat). In most fields, it has been replaced by the joule, the SI unit of energy.
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Sugars, brown
Nutritional value per 100 g (3.5 oz)
Energy 0 kcal 0 kJ
Carbohydrates 97.33 g
- Sugars 96.21 g
- Dietary fiber 0 g
Fat 0 g
Protein 0 g
Water 1.77 g
Thiamin (Vit. B1) 0.
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Nutritional value per 100 g (3.5 oz)
Energy 0 kcal 0 kJ
Carbohydrates 97.33 g
- Sugars 96.21 g
- Dietary fiber 0 g
Fat 0 g
Protein 0 g
Water 1.77 g
Thiamin (Vit. B1) 0.
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