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Sucralose

CAS No.
56038-13-2
Chemical Name:
Sucralose
Synonyms
TGS;ctopyranoside;loro-4-deoxy-;TRICHLOROSUCROSE;Sucralose 0.1;Sucralose CRS;Sucralose in stock GMP Factory;4,1’,6’-trichloro-4,1’,6’-trideoxy-galacto-sucrose;E955;ucralose
CBNumber:
CB9363034
Molecular Formula:
C12H19Cl3O8
Molecular Weight:
397.63
MDL Number:
MFCD03648615
MOL File:
56038-13-2.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-06-24 18:39:39
Product description Number Pack Size Price
Sucralose European Pharmacopoeia (EP) Reference Standard Y0001344 550 mg $254
Sucralose granular EMPROVE?ESSENTIALPhEur,NF,JPE 1.00895 10g $34.6
Sucralose ≥98.0% (HPLC) 69293 100g $183
Sucralose United States Pharmacopeia (USP) Reference Standard 1623626 400mg $489
Sucralose granular EMPROVE?ESSENTIALPhEur,NF,JPE 1.00895 1kg $522
More product size

Sucralose Properties

Melting point 115-1018°C
Boiling point 104-107 C
alpha D +68.2° (c = 1.1 in ethanol)
Density 1.375 g/cm
vapor pressure 0Pa at 25℃
refractive index 1.604
storage temp. 2-8°C
solubility DMF: 30 mg/ml
DMSO: 30 mg/mlPBS (pH 7.2): 1 mg/ml
form Powder
pka 12.52±0.70(Predicted)
color White
PH 6-8 (100g/l, H2O, 20°C)
Odor wh. cryst. powd., odorless, sweet taste
optical activity [α]/D 86.0±2.0°, c = 1 in H2O
Water Solubility Soluble in Water.
Merck 14,8880
BRN 3654410
Henry's Law Constant 2.5×1013 mol/(m3Pa) at 25℃, HSDB (2015)
Stability Hygroscopic
Major Application cleaning products
cosmetics
food and beverages
personal care
Cosmetics Ingredients Functions SKIN CONDITIONING
InChI 1S/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/t4-,5-,6+,7-,8+,9-,10+,11-,12+/m1/s1
InChIKey BAQAVOSOZGMPRM-QBMZZYIRSA-N
SMILES OC[C@H]1O[C@H](O[C@]2(CCl)O[C@H](CCl)[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1Cl
LogP -0.51 at 20℃
CAS DataBase Reference 56038-13-2(CAS DataBase Reference)
Substances Added to Food (formerly EAFUS) SUCRALOSE
FDA 21 CFR 101.80; 172.831
EWG's Food Scores 1
FDA UNII 96K6UQ3ZD4
EPA Substance Registry System .alpha.-D-Galactopyranoside, 1,6-dichloro-1,6-dideoxy-.beta.-D-fructofuranosyl 4-chloro-4-deoxy- (56038-13-2)
UNSPSC Code 85151701
NACRES NA.25

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P301+P312-P302+P352-P304+P340-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-37/39-24/25
WGK Germany  3
RTECS  LW5440140
HS Code  2932 14 00
Storage Class 11 - Combustible Solids
Hazardous Substances Data 56038-13-2(Hazardous Substances Data)
Toxicity LD50 orally in Rabbit: > 10000 mg/kg
REACH Registrations Active

Sucralose price More Price(101)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich Y0001344 Sucralose European Pharmacopoeia (EP) Reference Standard 56038-13-2 550 mg $254 2026-04-30 Buy
Sigma-Aldrich 1.00895 Sucralose granular EMPROVE?ESSENTIALPhEur,NF,JPE 56038-13-2 10g $34.6 2026-04-30 Buy
Sigma-Aldrich 69293 Sucralose ≥98.0% (HPLC) 56038-13-2 100g $183 2026-04-30 Buy
Sigma-Aldrich 1623626 Sucralose United States Pharmacopeia (USP) Reference Standard 56038-13-2 400mg $489 2026-04-30 Buy
Sigma-Aldrich 1.00895 Sucralose granular EMPROVE?ESSENTIALPhEur,NF,JPE 56038-13-2 1kg $522 2026-04-30 Buy
Product number Packaging Price Buy
Y0001344 550 mg $254 Buy
1.00895 10g $34.6 Buy
69293 100g $183 Buy
1623626 400mg $489 Buy
1.00895 1kg $522 Buy

Sucralose Chemical Properties,Uses,Production

Description

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.

Chemical Properties

Sucralose is a white to off-white colored, free-flowing, crystalline powder.

History

In 1975, sucralose was discovered by scientists from Tate & Lyle, working with researchers Leslie Hough and Shashikant Phadnis at Queen Elizabeth College (now part of King's College London). While looking for ways to use sucrose as a chemical intermediate, mixing sulfuryl chloride with sugar, Phadnis was told to "test" a chlorinated sugar compound. According to an anecdotal account, Phadnis thought Hough asked him to "taste" it, so he did and found the compound to be exceptionally sweet.
Sucralose was first approved for use in Canada in 1991. Subsequent approvals came in Australia in 1993, in New Zealand in 1996, in the United States in 1998, and in the European Union in 2004. By 2008, it had been approved in over 80 countries, including Mexico, Brazil, China, India, and Japan. In 2006, the FDA amended the regulations for foods to include sucralose as a "non-nutritive sweetener" in food.

Uses

High intensity sweetener manufactured by replacing three hydroxyl groups on the sucrose molecule with three chlorine atoms. The results are a sweetener of 0 cal that is not digested. It is 600 times as sweet as sugar with a similar flavor profile. It is heat stable, readily soluble, and maintains its stability at elevated temperatures. It has been approved for use in specific categories that include baked products, beverages, confectioneries, and certain desserts and toppings.

Uses

A low-calorie artificial sweetener

Uses

antiprotozoal

Uses

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.

Production Methods

Sucralose may be prepared by a variety of methods that involve the selective substitution of three sucrose hydroxyl groups by chlorine. Sucralose can also be synthesized by the reaction of sucrose (or an acetate) with thionyl chloride.

Definition

ChEBI: A disaccharide derivative consisting of 4-chloro-4-deoxy-alpha-D-galactopyranose and 1,6-dichloro-1,6-dideoxy-beta-D-fructofuranose units linked by a glycosidic bond.

General Description

Certified pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to pharmacopeia primary standards.
Sucralose is a polar, chlorinated sugar synthesized from saccharose precursor. It is widely used as a sweetener in a number of food and beverage products.

Pharmaceutical Applications

Sucralose is used as a sweetening agent in beverages, foods, and pharmaceutical applications. It has a sweetening power approximately 300–1000 times that of sucrose and has no aftertaste. It has no nutritional value, is noncariogenic, does not promote dental caries, and produces no glycemic response.

Biochem/physiol Actions

A synthetic sweet tastant detectable by humans. Activates T1R2/T1R3 sweet taste receptors on enteroendocrine cells and elicits increased hormonal secretion of glucagon-like peptide-1 and glucose-dependent insulinotrophic peptide.

Safety

Sucralose is generally regarded as a nontoxic and nonirritant material and is approved, in a number of countries, for use in food products. Following oral consumption, sucralose is mainly unabsorbed and is excreted in the feces.
The WHO has set an acceptable daily intake for sucralose of up to 15 mg/kg body-weight.
LD50 (mouse, oral): > 16 g/kg
LD50 (rat, oral): > 10 g/kg

storage

Sucralose is a relatively stable material. In aqueous solution, at highly acidic conditions (pH < 3), and at high temperatures (≤35℃), it is hydrolyzed to a limited extent, producing 4-chloro-4- deoxygalactose and 1,6-dichloro-1,6-dideoxyfructose. In food products, sucralose remains stable throughout extended storage periods, even at low pH. However, it is most stable at pH 5–6.
Sucralose should be stored in a well-closed container in a cool, dry place, at a temperature not exceeding 21℃. Sucralose, when heated at elevated temperatures, may break down with the release of carbon dioxide, carbon monoxide, and minor amounts of hydrogen chloride.

Regulatory Status

The FDA, in April 1998, approved sucralose for use as a tabletop sweetener and as an additive in a variety of food products. In the UK, sucralose was fully authorized for use in food products in 2005. It is also accepted for use in many other countries worldwide. Included in the Canadian List of Acceptable Nonmedicinal Ingredients.

References

[1] SUSAN S SCHIFFMAN K I R. Sucralose, a synthetic organochlorine sweetener: overview of biological issues.[J]. Journal of Toxicology and Environmental Health-Part B-Critical Reviews, 2013, 16 7: 399-451. DOI: 10.1080/10937404.2013.842523
[2] KNUT ERIK TOLLEFSEN  Duane B H  Luca Nizzetto. Presence, fate and effects of the intense sweetener sucralose in the aquatic environment[J]. Science of the Total Environment, 2012, 438: Pages 510-516. DOI: 10.1016/j.scitotenv.2012.08.060

105066-21-5
56038-13-2
Synthesis of Sucralose from Sucralose 6-Acetate
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Related Qustion

Ask a question
Q:Is sucralose safety in high temperature?Theon - Mar 30,2026
A:Research found that when sucralose is exposed to high temperatures (higher than 120℃) for long periods, chlorine can migrate from sucralose and potentially form chlorinated compounds. Therefore, during high-temperature cooking, it is best to avoid using ingredients containing sucralose.

View Lastest Price from Sucralose manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Sucralose pictures 2026-07-30 Sucralose
56038-13-2
0.99 RongNa Biotechnology Co.,Ltd
Sucralose pictures 2026-07-30 Sucralose
56038-13-2
1kg >99% HPLC 1000kg Changsha Staherb Natural Ingredients Co., Ltd.
Sucralose pictures 2026-07-30 Sucralose
56038-13-2
$400.00-1000.00 1ton 99% 5000 HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
  • Sucralose pictures
  • Sucralose
    56038-13-2
  • 0.99
  • RongNa Biotechnology Co.,Ltd
  • Sucralose pictures
  • Sucralose
    56038-13-2
  • $0.00
  • >99% HPLC
  • Changsha Staherb Natural Ingredients Co., Ltd.
  • Sucralose pictures
  • Sucralose
    56038-13-2
  • $400.00-1000.00
  • 99%
  • HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
1,6-dichloro-1,6-dideoxy-beta-d-fructofuranosyl4-chloro-4-deoxy-alpha-d-gala 4,1’,6’-trichloro-4,1’,6’-trideoxy-galacto-sucrose alpha-d-galactopyranoside,1,6-dichloro-1,6-dideoxy-beta-d-fructofuranosyl4-ch ctopyranoside Sucralose in stock GMP Factory 1,6-dichloro-1 4,1',6'-trichlorogalactosucrose loro-4-deoxy- 1,6-DICHLORO-1,6-DIDEOXY-BETA-D-FRUCTOFURANOSYL-4-CHLORO-4-DEOXY-ALPHA-D-GALACOTOPYRANOSIDE 1,6-Dichloro-1,6-dideoxy-beta-D-fructofuranosyl 4-chloro-4-deoxy-alpha-D-galactose SUCRALOSE 1,6-Dichloro-1,6-dideoxy-beta-D-fructofuranosyl-4-chloro-4-deoxy-alpha-D-galactopyranoside SUCRALOSE FCC (TRICHLOROGALACTOSUCROSE) SucraloseC12H19Cl3O8 Sucralose98%Min. Sucralose99% Steviosides90% Sucralose&Int. SPLENDA [R] .alpha.-D-Galactopyranoside, 1,6-dichloro-1,6-dideoxy-.beta.-D-fructofuranosyl 4-chloro-4-deoxy- trichlorogalactosucrose 4,16trichloro-4,16trideoxy pentagalactosucrose SUCRALOSE /4,1'',6'',-TRICHLORO-4,1'',6''TRIDEOXY-PENTAGALACTOSUCROSE SUCRALOSE(TRICHLOROSUCROSE) Sucralose 98.0-102.0% 4,1,6-TRICHLOROGALACTOSUCROSE (SUCRALOSE) 1,6-Dichloro-1,6-dideoxy-β-D-fructofuranosyl-4-chloro-4-deoxy-α-D-galacotopyranoside 1,6-Dichloro-1,6-Dideoxy-B-D-Fructofuranosyl-4-Chloro-4-Deoxy-A-D-Galacotopyranoside (2R,3R,4R,5R,6R)-2-{[(2S,3R,4R,5R)-2,5-Bis(chloromethyl)-3,4-dihydroxytetrahydro furan-2-yl]oxy}- Sucralose 0.1 α-D-Galactopyranoside, 1,6-dichloro-1,6-dideoxy-β-D-fructofuranosyl 4-chloro-4-deoxy- E955,Trichlorosucrose (2R,3R,4R,5R,6R)-2-{[(2S,3R,4R,5R)-2,5-Bis(chloromethyl)-3,4-dihydroxytetrahydrofuran-2-yl]oxy}-5-chloro-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4-diol (Sucralose) E955, Trichlorosucrose, 1,6-Dichloro-1,6-dideoxy-β-D-fructofuranosyl-4-chloro-4-deoxy-α-D-galactopyranoside 4,1’,6’-trichloro-galactosucorose trichlorosucorose 1',4,6'-Trichloro-galacto-sucrose 1,6-Dichloro-1,6-dideoxy-β-D-fructofuranosyl 4-chloro-4-deoxy-α-D-galactopyranoside (2R,3R,4R,5R,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 (2R,3R,4R,5R,6R)-2-[(2R,3S,4S,5S)-2,5-bis(chloromethyl)-3,4-dihydroxyoxolan-2-yl]oxy-5-chloro-6-(hydroxymethyl)oxane-3,4-diol (2R,3R,4R,5R,6R)-2-[(2R,3S,4S,5S)-2,5-bis(chloromethyl)-3,4-dihydroxy-tetrahydrofuran-2-yl]oxy-5-chloro-6-methylol-tetrahydropyran-3,4-diol (2R,3R,4R,5R,6R)-2-((2R,3S,4S,5S)-2,5-Bis(Chloromethyl)-3,4-Dihydroxytetrahydrofuran-2-Yloxy)-5-Chloro-6-(Hydroxymethyl)Tetrahydro-2H-Pyran-3,4-Diol SUBERIC ACID(RG) E955 Sucralose,1,6-Dichloro-1,6-dideoxy-β-D-fructofuranosyl-4-chloro-4-deoxy-α-D-galactopyranoside, E955, Trichlorosucrose Sucralose (400 mg) Sucralose (400 mg)G1E3170.998mg/mg(ai) Sucralose, FCC Sucralose, NF 2-{[2,5-bis(chloroMethyl)-3,4-dihydroxyoxolan-2-yl]oxy}-5-chloro-6-(hydroxyMethyl)oxane-3,4-diol 1-(1,6-Dichloro-1,6-dideoxy-beta-D-fructofuranosyl)-4-chloro-4-deoxy-alpha-D-galactopyranoside SUCRALOSE(P) Sucralose ,98% Sucralose (E955 Sucralose > Sucralose Standard a-D-Galactopyranoside, 1,6-dichloro-1,6-dideoxy-b-D-fructofuranosyl4-chloro-4-deoxy- Sucralose USP/EP/BP