2,5-Dihydroxy-1,4-dithiane(DHDT) - ≥97% , CAS No.40018-26-6

CAS: 40018-26-6 Cat. No.: D103137 Fórmula: C4H8O2S2 Peso molecular: 152.24 Beilstein Registry Number: 104402 Número CE: 254-751-6
Disponível para encomenda
GRADE & PURITY ≥97% cis- and trans- mixture
Synonyms
1,4 dithiane-2,5 diol | Dithian | EINECS 254-751-6 | FT-0610379 | F0001-1126 | NSC106280 | NSC-106280 | 2,5-Dihydroxy-1,4-dithiane | Mercaptoacetaldehyde dimer | CHEBI:179581 | FEMA 3826 | R4F79F1JB0 | STL185668 | J-523875 | 4-dithiane-2,5-diol | AMY24076
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
★
Size
Alemanha (EU)
USA*
Price
Qty
25g
D103137-25g
Sob encomenda · 8–12 semanas
8,59€
100g
D103137-100g
—
3 Em stock
17,27€
500g
D103137-500g
—
1 Em stock
51,98€
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥97%, cis- and trans- mixture for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Argon charged 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Visão geral

1,4-Dithiane-2,5-diol undergoes bifunctional squaramide catalyzed sulfa-Michael/aldol cascade reaction with chalcones to afford trisubstituted tetrahydrothiophenes.It participates in diastereoselective [3+3] cycloaddition with azomethine imines catalyzed by 1,4-diazabicyclo[2.2.2]octane.It is a mercaptoacetaldehyde dimer and an efficient synthon for incorporating a thiol group to in situ generated nitroalkenes.
1,4-Dithiane-2,5-diol was used in the synthesis of: · substituted tetrahydrothiophene derivatives; · 2-amino-3-(arylsulfonyl)thiophenes, potential antiviral and antitumor agents.

Specifications

Sinónimos
1,4 dithiane-2,5 diol | Dithian | EINECS 254-751-6 | FT-0610379 | F0001-1126 | NSC106280 | NSC-106280 | 2,5-Dihydroxy-1,4-dithiane | Mercaptoacetaldehyde dimer | CHEBI:179581 | FEMA 3826 | R4F79F1JB0 | STL185668 | J-523875 | 4-dithiane-2,5-diol | AMY24076
Especificações e pureza
≥97%, cis- and trans- mixture
Aplicação
1,4-Dithiane-2,5-diol was used in the synthesis of: substituted tetrahydrothiophene derivatives 2-amino-3-(arylsulfonyl)thiophenes, potential antiviral and antitumor agents
Condições de armazenamento de armazenamento
Store at 2-8°C,Argon charged
Enviado em
Wet ice
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Pureza
≥97%
Nomes e identificadores
Pubchem Sid508807771
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/508807771
Sorrisos canónicosC1C(SCC(S1)O)O
IUPAC Name1,4-dithiane-2,5-diol
InChIKeyYUIOPHXTILULQC-UHFFFAOYSA-N
INCHI1S/C4H8O2S2/c5-3-1-7-4(6)2-8-3/h3-6H,1-2H2
SMILES isoméricas C1C(SCC(S1)O)O
WGK Alemanha 2
Número UN 3335
Peso molecular 152.24
Beilstein 104402
Reaxy-Rn 104402
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=104402&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
SuperclassOrganoheterocyclic compounds
ClasseDithianes
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentDithianes
Alternative Parents Organooxygen compounds  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents 1,4-dithiane - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aliphatic heteromonocyclic compound
DescriçãoThis compound belongs to the class of organic compounds known as dithianes. These are compounds containing a dithiane moiety, which is composed of a cyclohexane core structure wherein two methylene units are replaced by sulfur centres.
External Descriptors Not available
Estrutura 3D
Modelo de Estrutura Química Interativa





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.

9 results found

Lot NumberCertificate TypeDataItem
H2627766Certificate of AnalysisAug 07, 2026 D103137
H2627767Certificate of AnalysisAug 07, 2026 D103137
I2603872Certificate of AnalysisAug 07, 2026 D103137
F2629058Certificate of AnalysisJul 09, 2026 D103137
H2512133Certificate of AnalysisAug 21, 2025 D103137
H2627771Certificate of AnalysisJul 11, 2024 D103137
C2003150Certificate of AnalysisDec 15, 2023 D103137
I1510021Certificate of AnalysisMay 06, 2023 D103137
C2317434Certificate of AnalysisMar 22, 2023 D103137
Propriedades químicas e físicas
SensibilidadeLight & Moisture Sensitive;heat sensitive
Ponto de fusão (°C)130°C
Peso molecular152.200 g/mol
XLogP30.300
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count0
Exact Mass151.997 Da
Monoisotopic Mass151.997 Da
Topological Polar Surface Area91.100 Ų
Heavy Atom Count8
Formal Charge0
Complexity68.400
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count2
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calculadoras de soluções
Revisões

Avaliações dos Clientes

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.