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Sucralose is Off-White Amorphous Solid, while it's Molecular Formula is C12H19Cl3O8. Sucralose (1,6-dichloro-1,6-dideoxy-p-fructofuranosyl-4-chloro-oc- D-galactopyra- noside) is a nonnutritive sweetener based on sucrose. It is selectively chlorinated and the glycoside link between the two rings is resistant to hydrolysis by acid or enzymes, so it is not metabolized. It has 400 to 800 times the sweetness of sucrose, is very soluble in water, and is stable in heat. It can be used in food products that are baked or fried. Sucralose is produced by the selective chlorination of the sucrose molecule using a patented process by Tate and LyIe that replaces the three hydroxyl groups (OH) with three chlorine (Cl) atoms. This modified sugar is minimally absorbed by the body and passes out unchanged. It was approved for use in foods and beverages in 1999 in the United States.
The CAS number of Sucralose is 56038-13-2.
More information of Sucralose 56038-13-2 are:
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Synonyms |
Trichlorosucrose;4,1,6-Trichloro-4,1,6-trideoxy-galacto-sucrose;1,6-Dichloro-1,6-dideoxy-beta-D-fructofuranosyl 4-chloro-4-deoxy-alpha-D-galactose;1,6-Dichloro-1,6-dideoxy-beta-D-fructofuranosyl 4-chloro-4-deoxy-alpha-D-galactopyranoside;See R-D-Galactopyranoside,1,6-dichloro-1,6- dideoxy-a-D-fructofuranosyl 4-chloro-4-deoxy-;Sucralose (Trichlorosucorose);Sucralose Fccv;Sucralose [BAN];(2R,3R,4R,5S,6R)-2-[(2R,3S,4S,5S)-2,5-bis(chloromethyl)-3,4-dihydroxy-oxolan-2-yl]oxy-5-chloro-6-(hydroxymethyl)oxane-3,4-diol; |
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CAS Number |
56038-13-2 |
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Molecular Formula |
C12H19Cl3O8 |
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Molecular Weight |
397.637 |
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Density |
1.69 g/cm3 |
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Melting Point |
125.5oC |
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Boiling Point |
669.4 °C at 760 mmHg |
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Flash Point |
358.7 °C |
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HS CODE |
2932 14 00 |
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PSA |
128.84000 |
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LogP |
-1.65610 |
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Pka |
12.52±0.70(Predicted) |
Sucralose is the only non-caloric sweetener made from sugar. It is in fact the latest non nutritive sweetener to have been approved by US FDA and other regulatory bodies and have hit the markets . Sucralose is derived from sugar through a multi-step patented manufacturing process that selectively substitutes three atoms of chlorine for three hydroxyl groups on the sugar molecule. This change produces a sweetener that has no calories, yet is 600 times sweeter than sucrose, making it roughly twice as sweet as saccharin and four times as sweet as aspartame.
InChI:InChI=1/C12H19Cl3O8/c13-1-4-7(17)10(20)12(3-14,22-4)23-11-9(19)8(18)6(15)5(2-16)21-11/h4-11,16-20H,1-3H2
Articles related to Sucralose:
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Article |
Source |
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Bioconversion of sucralose-6-acetate to sucralose using immobilized microbial cells |
Chaubey, Asha,Raina, Chand,Parshad, Rajinder,Rouf, Abdul,Gupta, Pankaj,Taneja, Subhash C. , p. 81 - 86 (2013) |
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Recrystallization method of sucrose-6-acetate and applications thereof |
- Paragraph 0052; 0053; 0058, (2017/09/01) |
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