Allitol - ≥98%, used for Allitol is a rare natural polyol that can be used as a sweetener. Allitol is an important intermediate for the preparation of the agents which against diabetes, cancer, and viral infections, including AIDS. various applications ,

CAS: 488-44-8 Cat. No.: A121073 Summenformel: C6H14O6 Molekulargewicht: 182.17 Beilstein Registry Number: 1(4)2839
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GRADE & PURITY ≥98%
Synonyms
B3F996O6JU | s9347 | ALLIT | (2R,3R,4S,5S)-hexane-1,2,3,4,5,6-hexol;Dulcitol | CCG-266440 | L-Allitol | Allodulcit | X9X | DTXSID60197607 | Allitol, >=98% | Allodulcitol | WURCS=2.0/1,1,0/[h2222h]/1/ | Allitol | A832929 | CHEBI:181263 | UNII-B3F996O6JU |
Storage
Store at 2-8°C,Protected from light
Shipped In
Wet ice
★
Size
Deutschland (EU)
USA*
Price
Qty
25mg
A121073-25mg
—
2 Auf Lager

32,89€

49,37€
Speichern 16,49 € (33.39%)
100mg
A121073-100mg
—
2 Auf Lager

103,17€

155,24€
Speichern 52,06 € (33.54%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Protected from light Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

Allitol, a water retentive rare sugar alcohol, may be used as a monosaccharide laxative. Allitol may be used as a reference compound during separation and analysis of hexitols such as galactitol, iditol, altritols, sorbitol and mannitol.

Specifications

Synonyme
B3F996O6JU | s9347 | ALLIT | (2R,3R,4S,5S)-hexane-1,2,3,4,5,6-hexol;Dulcitol | CCG-266440 | L-Allitol | Allodulcit | X9X | DTXSID60197607 | Allitol, >=98% | Allodulcitol | WURCS=2.0/1,1,0/[h2222h]/1/ | Allitol | A832929 | CHEBI:181263 | UNII-B3F996O6JU |
Spezifikationen & Reinheit
≥98%
Anmeldung
Allitol is a rare natural polyol that can be used as a sweetener. Allitol is an important intermediate for the preparation of the agents which against diabetes, cancer, and viral infections, including AIDS.
Storage
Store at 2-8°C,Protected from light
Verschickt in
Wet ice
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Reinheit
≥98%
Namen und Kennungen
Pubchem Sid504756837
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504756837
Kanonisches LächelnC(C(C(C(C(CO)O)O)O)O)O
IUPAC Name(2R,3R,4S,5S)-hexane-1,2,3,4,5,6-hexol
InChIKeyFBPFZTCFMRRESA-FBXFSONDSA-N
INCHI1S/C6H14O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3-12H,1-2H2/t3-,4+,5-,6+
Isomere SMILES C([C@H]([C@H]([C@H]([C@H](CO)O)O)O)O)O
WGK Deutschland 3
RTECS BA1840000
Molekulargewicht 182.17
Beilstein 1(4)2839
Reaxy-Rn 8496933
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8496933&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
KlasseOrganooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Not available
Direct ParentSugar alcohols
Alternative Parents Monosaccharides  Secondary alcohols  Polyols  Primary alcohols  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Sugar alcohol - Monosaccharide - Secondary alcohol - Polyol - Hydrocarbon derivative - Primary alcohol - Alcohol - Aliphatic acyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as sugar alcohols. These are hydrogenated forms of carbohydrate in which the carbonyl group (aldehyde or ketone, reducing sugar) has been reduced to a primary or secondary hydroxyl group.
External Descriptors Not available
3D-Struktur
Interaktives chemisches Strukturmodell





Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

5 results found

Lot NumberCertificate TypeDatumArtikel
K2212100Certificate of AnalysisAug 04, 2026 A121073
J2424396Certificate of AnalysisOct 14, 2024 A121073
A2426423Certificate of AnalysisJan 16, 2024 A121073
A2426426Certificate of AnalysisJan 16, 2024 A121073
K2212147Certificate of AnalysisSep 05, 2022 A121073
Chemische und physikalische Eigenschaften
LöslichkeitDMSO: 50 mg/mL (274.47 mM)
EmpfindlichkeitLight sensitive;Moisture sensitive
Schmelzpunkt (°C)152 °C
Molekulargewicht182.170 g/mol
XLogP3-3.100
Hydrogen Bond Donor Count6
Hydrogen Bond Acceptor Count6
Rotatable Bond Count5
Exact Mass182.079 Da
Monoisotopic Mass182.079 Da
Topological Polar Surface Area121.000 Ų
Heavy Atom Count12
Formal Charge0
Complexity105.000
Isotope Atom Count0
Defined Atom Stereocenter Count4
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referenzen
1. Lei Wang, Kecai Chen, Peng Zheng, Xiang Huo, Fei Liao, Liping Zhu, Meirong Hu, Yong Tao.  (2022)  Enhanced production of D-psicose from D-fructose by a redox-driven multi-enzyme cascade system.  ENZYME AND MICROBIAL TECHNOLOGY,      [PMID:36481542] [10.1016/j.enzmictec.2022.110172]
2. Xue-Feng Shao, Chao Wang, Yong-Jian Yang, Biao Feng, Zi-Qin Zhu, Wu-Jun Wang, Yi Zeng, Li-Wu Fan.  (2018)  Screening of sugar alcohols and their binary eutectic mixtures as phase change materials for low-to-medium temperature latent heat storage. (Ⅰ): Non-isothermal melting and crystallization behaviors.  ENERGY,      [PMID:] [10.1016/j.energy.2018.07.081]
Lösungsrechner
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