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1109-28-0

O-α-D-glucopyranosyl-(1→4)-O-α-D-glucopyranosyl-(1→4)-O-α-D-glucopyranose

CAS: 1109-28-0

Molecular Formula: C18H32O16

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1109-28-0 - Names and Identifiers

Name O-α-D-glucopyranosyl-(1→4)-O-α-D-glucopyranosyl-(1→4)-O-α-D-glucopyranose
Synonyms Maltotriose
MALTOTRIOSE, D-(+)-(RG)
4-O-[4-O-(α-D-Glucopyranosyl)-α-D-glucopyranosyl]-D-glucose
(+)-4-O-(4-O-α-D-Glucopyranosyl-α-D-glucopyranosyl)-D-glucose
O-α-D-glucopyranosyl-(1→4)-O-α-D-glucopyranosyl-(1→4)-O-α-D-glucopyranose
D-Glucose, O-.alpha.-D-glucopyranosyl-(1?4)-O-.alpha.-D-glucopyranosyl-(1?4)-
O-α-DD-Glucopyranosyl-(1-4)-O-α-D-glucopyranosyl-(1-4)-D-glucose, α-D-Glc-(1-4)-α-D-Glc-(1-4)-D-Glc
4-[3,4-dihydroxy-6-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-oxan-2-yl]oxy-2,3,5,6-tetrahydroxy-hexanal
CAS 1109-28-0
EINECS 214-174-2
InChI InChI=1/C18H32O16/c19-1-4-7(22)8(23)12(27)17(31-4)34-15-6(3-21)32-18(13(28)10(15)25)33-14-5(2-20)30-16(29)11(26)9(14)24/h4-29H,1-3H2/t4-,5-,6-,7-,8+,9-,10-,11-,12-,13-,14-,15-,16?,17-,18-/m1/s1
InChIKey FYGDTMLNYKFZSV-DZOUCCHMSA-N

1109-28-0 - Physico-chemical Properties

Molecular FormulaC18H32O16
Molar Mass504.44
Density1.4403 (rough estimate)
Melting Point132-135 °C
Boling Point513.84°C (rough estimate)
Specific Rotation(α)160 ° (C=2, H2O)
Flash Point477°C
Water SolubilitySoluble in water.
Solubility Solubility in water: 50 mg/mL, colorless and transparent aqueous solution.
Vapor Presure6.5E-35mmHg at 25°C
AppearanceWhite powder
ColorWhite to Off-white
BRN1443481
pKa12.39±0.20(Predicted)
Storage ConditionSealed in dry,2-8°C
StabilityStable. Combustible. Incompatible with strong oxidizing agents.
Refractive Index1.6760 (estimate)
MDLMFCD00006629
Physical and Chemical PropertiesHydrolysis of the starch exudate of Saccharomyces cerevisiae. Solubility in water: 50 mg/mL, colorless and transparent aqueous solution. Specific rotation [a]20/D :162.5 °(c = 1, H2O).

1109-28-0 - Risk and Safety

Safety Description24/25 - Avoid contact with skin and eyes.
WGK Germany3
FLUKA BRAND F CODES10
HS Code29400090

1109-28-0 - Reference Information

Preparation method In nature, maltose mainly exists in germinated grains, especially malt, so this name is given. Under the action of starch invertase, starch undergoes a hydrolysis reaction to produce maltoglycan, which undergoes a hydrolysis reaction to produce two molecules of glucose. Maltoglycan is a series of low molecular weight sugars obtained by hydrolysis of starch. It is a linear group of α(1-4) linked D-glucose polymers. Usually maltose industrial grade products are made by acidic hydrolysis of potato starch. Maltotriose (Maltotriose) consists of α(1-4) linked D-glucose monomer condensation with a polymerization degree of 3.
main uses food gelatinization, pigment and brittle agent in food processing. Fabric finishing agents are used to increase the weight and stiffness of fabric fibers. Thickeners and adhesives for pharmaceutical and paper coatings.
Biological activity Maltotriose are common oligosaccharide metabolites, which are often found in human urine after ingestion of maltose.
use used for content determination/identification/pharmacological experiments, etc.
Last Update:2024-04-09 02:00:06
1109-28-0
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