U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C12H24O11
Molecular Weight 344.3124
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MALTITOL

SMILES

[H][C@@](O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)([C@H](O)CO)[C@H](O)[C@@H](O)CO

InChI

InChIKey=VQHSOMBJVWLPSR-WUJBLJFYSA-N
InChI=1S/C12H24O11/c13-1-4(16)7(18)11(5(17)2-14)23-12-10(21)9(20)8(19)6(3-15)22-12/h4-21H,1-3H2/t4-,5+,6+,7+,8+,9-,10+,11+,12+/m0/s1

HIDE SMILES / InChI

Description
Curator's Comment: Description was created based on several sources, including http://www.nutrientsreview.com/carbs/sugar-alcohols-maltitol.html | http://www.polyols-eu.com/maltitol

Maltitol is a sugar alcohol, or polyol. Small amounts of maltitol occur naturally in chicory leaves and in roasted malt. Commercially, maltitol is produced from the starch of cereals such as corn, potatoes and wheat. Manufacturers use the catalytic hydrogenation of D-maltose to make a hydrogenated disaccharide consisting of a glucose molecule and a sorbitol molecule bound together. Maltitol is used as a low-calorie sweetener, humectant, thickening agent and texturizer in candies, chocolates, baked goods, ice creams, chewing gums and pan-coated tablets. In the European Union maltitol is labeled as E number E965.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
69.0 mM [Ki]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Preventing
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Effects of oral administration of maltitol on plasma glucose, plasma sorbitol, and serum insulin levels in man.
1986 Mar 17
Carbohydrate-controlled precipitation of apatite with coprecipitation of organic molecules in human saliva: stabilizing role of polyols.
1989 Apr
A high-performance liquid chromatography method for the analysis of picomole amounts of oligosaccharides.
1989 May 1
Polyol-combinant saliva stimulants: a 4-month pilot study in young adults.
1998 Apr
Phosphorylation and metabolism of sucrose and its five linkage-isomeric alpha-D-glucosyl-D-fructoses by Klebsiella pneumoniae.
2001 Mar 22
Interaction of methylparaben preservative with selected sugars and sugar alcohols.
2002 Jul
Sugar alcohols enhance calcium transport from rat small and large intestine epithelium in vitro.
2002 Jun
Plasticized waxy maize starch: effect of polyols and relative humidity on material properties.
2002 Sep-Oct
Health potential of polyols as sugar replacers, with emphasis on low glycaemic properties.
2003 Dec
Cloning and characterization of two alpha-glucosidases from Bifidobacterium adolescentis DSM20083.
2003 Mar
Chemoenzymatically synthesized glycoconjugate polymers.
2003 Mar-Apr
NMR and quantum chemical study on the OH...pi and CH...O interactions between trehalose and unsaturated fatty acids: implication for the mechanism of antioxidant function of trehalose.
2003 Oct 22
Alternative sugars as potential carriers for dry powder inhalations.
2004 Feb 11
Characteristics of erythritol and formulation of a novel coating with erythritol termed thin-layer sugarless coating.
2004 Jul 8
Molecular mobility in amorphous maltose and maltitol from phosphorescence of erythrosin B.
2005 Aug 25
Dynamic site heterogeneity in amorphous maltose and maltitol from spectral heterogeneity in erythrosin B phosphorescence.
2005 Dec 12
Combined NMR and quantum chemical studies on the interaction between trehalose and dienes relevant to the antioxidant function of trehalose.
2005 Feb 24
Oxygen solubility and permeability of carbohydrates.
2005 Jun 13
Human gut microbiota does not ferment erythritol.
2005 Nov
The cytogenetic effects of food sweetener maltitol in human peripheral lymphocytes.
2006
The effect of liquorice extract-containing starch gel on the amount and microbial composition of plaque.
2006 Jun
Genetic requirements for growth of Escherichia coli K12 on methyl-alpha-D-glucopyranoside and the five alpha-D-glucosyl-D-fructose isomers of sucrose.
2006 Jun 30
Medicinal carbon tablets for treatment of acetaminophen intoxication: adsorption characteristics of medicinal carbon powder and its tablets.
2006 Mar
Linear response of mutans streptococci to increasing frequency of xylitol chewing gum use: a randomized controlled trial [ISRCTN43479664].
2006 Mar 24
Considerations about the theoretically expected crushing strength of tablets from binary powder mixtures: double layer tablets versus arithmetic additivity rule.
2006 Nov
Decreased salivary uptake of [14C]-xylitol after a four-week xylitol chewing gum regimen.
2007
Improved postprandial response and feeling of satiety after consumption of low-calorie muffins with maltitol and high-amylose corn starch.
2007 Aug
Suppressive effect of partially hydrolyzed guar gum on transitory diarrhea induced by ingestion of maltitol and lactitol in healthy humans.
2007 Sep
Ecology of lactobacilli in the oral cavity: a review of literature.
2008
High pressure study on molecular mobility of leucrose.
2008 Aug 28
Impact of sugar replacers on cognitive performance and function in rats.
2008 Nov
Standards of medical care in diabetes--2009.
2009 Jan
Sugar alcohols, caries incidence, and remineralization of caries lesions: a literature review.
2010
A randomized cross-over study to evaluate the swallow-enhancing and taste-masking properties of a novel coating for oral tablets.
2010 Aug
[Preparation of orally disintegrating tablets for masking of unpleasant taste: comparison with corrective-adding methods].
2010 Jan
Standards of medical care in diabetes--2010.
2010 Jan
Complete genome sequence of Nocardiopsis dassonvillei type strain (IMRU 509).
2010 Nov 30
[Comparative effects of the maltitol chewing gums on reducing plaque].
2010 Oct
Patents

Sample Use Guides

5.0% maltitol for 8 weeks significantly suppressed weight gain, hepatic fatty degeneration, hyperglycemia, and hypercholesterolemia in a mouse high-fat diet model.
Route of Administration: Oral
Maltitol (1.25, 2.5, and 5 mg/mL) has a weak genotoxic potential and it appears non-cytotoxic to human peripheral lymphocytes in vitro.
Name Type Language
MALTITOL
EP   FCC   II   INCI   MART.   USP-RS  
INCI  
Official Name English
MALTITOL [II]
Common Name English
INS-965(I)
Code English
CERESTAR 16303
Common Name English
AMALTY MR 100
Common Name English
MALTITOL SOLUTION [NF]
Common Name English
SWEETPEARL P 200
Common Name English
MALTITOL SOLUTION
Common Name English
MALTISWEET 3145
Common Name English
MALBIT CH 16385
Common Name English
MALTITOL [FCC]
Common Name English
MALTITOL [INCI]
Common Name English
MALTITOL [EP MONOGRAPH]
Common Name English
MALTITOL [MART.]
Common Name English
HYDROGENATED HIGH MALTOSE-CONTENT GLUCOSE SYRUP
Common Name English
LYCASIN HBC
Common Name English
MALTIDEX CH 16385
Common Name English
INS NO.965(I)
Code English
DRIED MALTITOL SYRUP
Common Name English
MALTITOL SYRUP POWDER
Common Name English
HYDROGENATED MALTOSE
Common Name English
MALTITOL [USP-RS]
Common Name English
E-965(I)
Code English
Classification Tree Code System Code
CODEX ALIMENTARIUS (GSFA) INS-965(I)
Created by admin on Fri Dec 15 15:30:15 GMT 2023 , Edited by admin on Fri Dec 15 15:30:15 GMT 2023
DSLD 3248 (Number of products:4)
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JECFA EVALUATION INS-965(I)
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NCI_THESAURUS C283
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Code System Code Type Description
HSDB
7971
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PRIMARY
ChEMBL
CHEMBL63558
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MESH
C010745
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PRIMARY
ECHA (EC/EINECS)
209-567-0
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PRIMARY
EPA CompTox
DTXSID0044444
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PRIMARY
RS_ITEM_NUM
1374907
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PRIMARY
RXCUI
1363049
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PRIMARY RxNorm
PUBCHEM
493591
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PRIMARY
NCI_THESAURUS
C77138
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PRIMARY
DAILYMED
D65DG142WK
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PRIMARY
EVMPD
SUB12136MIG
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PRIMARY
FDA UNII
D65DG142WK
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PRIMARY
WIKIPEDIA
MALTITOL
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PRIMARY
CAS
585-88-6
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PRIMARY
SMS_ID
100000080142
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PRIMARY
CHEBI
68428
Created by admin on Fri Dec 15 15:30:15 GMT 2023 , Edited by admin on Fri Dec 15 15:30:15 GMT 2023
PRIMARY