D-(+)-Trehalose dihydrate - analytical standard , CAS No.6138-23-4

CAS: 6138-23-4 Cat. No.: T100011 Fórmula: C12H22O11·2H2O Peso molecular: 378.33 Beilstein Registry Number: 5322018 Número CE: 612-140-5
Disponível para encomenda
GRADE & PURITY Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods.
Synonyms
D-(+)-Trehalose dihydrate, for microbiology, >=99.0% | TREHALOSE, DIHYDRATE | (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-3,4,5-triol;dihydrate | a-d-glucopyranosyl-a-d-glucopyranoside | DPVH
Storage
Room temperature,Desiccated
Shipped In
Normal
★
Size
Alemanha (EU)
USA*
Price
Qty
250mg
T100011-250mg
—
5 Em stock
77,14€
1g
T100011-1g
Sob encomenda · 8–12 semanas
133,55€
5g
T100011-5g
Sob encomenda · 8–12 semanas
303,62€
Enter a quantity for the sizes you want to add.
🧪
Why this grade

analytical standard Analytical standard for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature,Desiccated Ships Normal 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 25 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
D-(+)-Trehalose dihydrate, for microbiology, >=99.0% | TREHALOSE, DIHYDRATE | (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-3,4,5-triol;dihydrate | a-d-glucopyranosyl-a-d-glucopyranoside | DPVH
Especificações e pureza
analytical standard
Condições de armazenamento de armazenamento
Room temperature,Desiccated
Enviado em
Normal
Grau
Analytical standard
Nomes e identificadores
Pubchem Sid
Sorrisos canónicos
[H]O[H].[H]O[H].OC[C@H]1O[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O
IUPAC Name
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-3,4,5-triol;dihydrate
InChIKey
DPVHGFAJLZWDOC-PVXXTIHASA-N
INCHI
1S/C12H22O11.2H2O/c13-1-3-5(15)7(17)9(19)11(21-3)23-12-10(20)8(18)6(16)4(2-14)22-12;;/h3-20H,1-2H2;2*1H2/t3-,4-,5-,6-,7+,8+,9-,10-,11-,12-;;/m1../s1
SMILES isoméricas
C([C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O[C@@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)O)O)O)O.O.O
WGK Alemanha
2
Peso molecular
378.33
Beilstein
5322018
Reaxy-Rn
5322018
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=5322018&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
ClasseOrganooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Glycosyl compounds
Direct ParentO-glycosyl compounds
Alternative Parents Disaccharides  Oxanes  Secondary alcohols  Polyols  Oxacyclic compounds  Acetals  Primary alcohols  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents O-glycosyl compound - Disaccharide - Oxane - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Polyol - Acetal - Organic oxide - Hydrocarbon derivative - Primary alcohol - Alcohol - Aliphatic heteromonocyclic compound
DescriçãoThis compound belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.
External Descriptors Not available
Estrutura 3D
Modelo de Estrutura Química Interativa





Mecanismos de ação
Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
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.

6 results found

Lot NumberCertificate TypeDataItem
K2103602Certificate of AnalysisMay 09, 2025 T100011
G1524072Certificate of AnalysisOct 21, 2024 T100011
J2514689Certificate of AnalysisMar 26, 2024 T100011
J2514690Certificate of AnalysisMar 26, 2024 T100011
J2515798Certificate of AnalysisMar 26, 2024 T100011
D1825018Certificate of AnalysisOct 13, 2023 T100011
Propriedades químicas e físicas
SensibilidadeHygroscopic.
Rotação específica [α]181 ° (C=7, H2O)
Ponto de fusão (°C)97-99°C
Peso molecular378.330 g/mol
XLogP3
Hydrogen Bond Donor Count10
Hydrogen Bond Acceptor Count13
Rotatable Bond Count4
Exact Mass378.137 Da
Monoisotopic Mass378.137 Da
Topological Polar Surface Area192.000 Ų
Heavy Atom Count25
Formal Charge0
Complexity348.000
Isotope Atom Count0
Defined Atom Stereocenter Count10
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count3
FAQs e artigos
How should laboratory strains be preserved?
Glucose Oxidase: A Versatile Biocatalyst Across Multiple Fields
Trehalose: Physicochemical Characteristics, Manufacturing Processes, and Application Guidelines
Phycocyanin: A Review of Sources, Structural Features, Production Processes, Applications, and Claimed Benefits
dsDNase-Mediated Hydrolysis of Double-Stranded DNA: Enzymatic Characteristics, Methodological Strategies, and Bioanalytical Applications
Functional Properties, Application Scenarios, and Manufacturing Processes of Maltotetraose (G4): A Review
Effects of Cell Sample Preservation Systems on Morphological Integrity, Anticoagulant Stability, and Analytical Results
The Moisturizing and Low-Moisture Protective Mechanisms of Trehalose: From Its α,α-1,1 Structure and Hydration Dynamics to In Vitro Skin Barrier Research
Exosome-Related Ingredients in Skincare Products: Sources and Preparation, Quality Control, Evidence of Efficacy, and Safety Assessment
Citations of This Product
Calculadoras de soluções
Revisões

Avaliações dos Clientes

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