Name: Trisulfure de diallyle - Moligand™,≥65% , CAS No.2050-87-5
SKU: D302734
Availability: InStock

Trisulfure de diallyle - Moligand™,≥65% , CAS No.2050-87-5

CAS: 2050-87-5 Cat. No.: D302734 Formule: C₆H₁₀S₃ Poids moléculaire: 178.34 Numéro CE: 218-107-8

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Trisulfure de diallyle - Moligand™,≥65% CAS No(2050-87-5) by Aladdin Scientific

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DISPONIBLE À COMMANDE

GRADE & PURITY Moligand™ ? ≥65%

Synonyms

Storage

Conserver à -20°C

Shipped In

Glacière + blocs de glace

Vue d’ensemble Specifications Noms et identifiants Documentation Advanced Data Taxonomic Classification Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques FAQ et articles Citations of This Product Calculateurs de solution Avis

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Why this grade

Moligand™,≥65% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Conserver à -20°C Ships Glacière + blocs de glace Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

Cited in 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Vue d’ensemble

Le trisulfure de diallyle, un composant de l'ail et des oignons, est un composé proapoptotique qui possède également une activité antioxydante.

Le trisulfure de diallyle a été utilisé pour étudier ses propriétés anti-cancérigènes dans des cellules de gliome et de cancer de la vessie

Specifications

Synonymes

Spécifications et pureté

Moligand™,≥65%

Mécanismes biochimiques et physiologiques

Composé organosulfuré. Augmente la production de glutathion S-transférase (GST) et présente des propriétés antimicrobiennes et chimioprotectrices.

Conditions de stockage de stockage

Conserver à -20°C

Expédié en

Glacière + blocs de glace

Grade

Moligand™

Type d'action

INHIBITOR

Note

Dans la mesure du possible, les solutions doivent être préparées et utilisées le même jour. Toutefois, si vous devez préparer des solutions de base à l'avance, nous vous recommandons de les conserver sous forme d'aliquotes dans des flacons hermétiques à -20°C. Ces aliquotes sont généralement utilisables pendant un mois. En général, ces solutions peuvent être utilisées pendant un mois. Avant utilisation, et avant d'ouvrir le flacon, nous vous recommandons de laisser votre produit s'équilibrer à température ambiante pendant au moins 1 heure. Besoin de plus de conseils sur la solubilité, l'utilisation et la manipulation ? Veuillez consulter notre page de questions fréquemment posées (FAQ) pour plus de détails.

Pureté

≥65%

Noms et identifiants

Pubchem Sid

528769681

Sourires canoniques

C=CCSSSCC=C

IUPAC Name

3-(prop-2-enyltrisulfanyl)prop-1-ene

InChIKey

UBAXRAHSPKWNCX-UHFFFAOYSA-N

INCHI

1S/C6H10S3/c1-3-5-7-9-8-6-4-2/h3-4H,1-2,5-6H2

Isomères SMILES

C=CCSSSCC=C

Poids moléculaire

178.34

Reaxy-Rn

1745734

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1745734&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

Kingdom Organic compounds
- Superclass Organosulfur compounds
  - Classe Organic trisulfides

Kingdom	Organic compounds
Superclass	Organosulfur compounds
Classe	Organic trisulfides
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Organic trisulfides
Alternative Parents	Allyl sulfur compounds Sulfenyl compounds Hydrocarbon derivatives
Molecular Framework	Aliphatic acyclic compounds
Substituents	Organic trisulfide - Allyl sulfur compound - Sulfenyl compound - Hydrocarbon derivative - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as organic trisulfides. These are organosulfur compounds with the general formula RSSSR' (R,R'=alkyl, aryl).
External Descriptors	organic trisulfide
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Structure 3D

Cibles associées (humaines)

TRPA1 Tclin Transient receptor potential cation channel subfamily A member 1 (1 Activities)

Discover Target: TRPA1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

VDR Tclin Vitamin D receptor (26531 Activities)

Discover Target: VDR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

Discover Target: ALDH1A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

FASN Tchem Fatty acid synthase (3390 Activities)

Discover Target: FASN

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GSR Tclin Glutathione reductase (335 Activities)

Discover Target: GSR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)

Discover Target: CYP3A4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)

Discover Target: APEX1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HPGD Tchem 15-hydroxyprostaglandin dehydrogenase [NAD+] (24926 Activities)

Discover Target: HPGD

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HBA1 Tclin Hemoglobin HbA (880 Activities)

Discover Target: HBA1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SCNN1A Tclin Amiloride-sensitive sodium channel, ENaC (10 Activities)

Discover Target: SCNN1A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Cibles associées (non humaines)

MDCK (10148 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GCN5 Histone acetyltransferase GCN5 (89 Activities)

Discover Target: GCN5

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Trpa1 Transient receptor potential cation channel subfamily A member 1 (1003 Activities)

Discover Target: Trpa1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)

Discover Target: ffp

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mécanismes d'action

Certificats (CoA, COO, BSE/TSE et tableau d'analyse)

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.

10 results found

Lot Number	Certificate Type	Date	Article
J2323063	Certificate of Analysis	Aug 03, 2026	D302734
C2618255	Certificate of Analysis	Mar 23, 2026	D302734
E2608335	Certificate of Analysis	Mar 07, 2026	D302734
E2608336	Certificate of Analysis	Mar 07, 2026	D302734
E2608337	Certificate of Analysis	Mar 07, 2026	D302734
F2129181	Certificate of Analysis	Apr 25, 2024	D302734
F2129183	Certificate of Analysis	Apr 25, 2024	D302734
K2419123	Certificate of Analysis	Apr 25, 2024	D302734
F2129182	Certificate of Analysis	Jul 05, 2021	D302734
J2511117	Certificate of Analysis	Jul 05, 2021	D302734

Propriétés chimiques et physiques

Poids moléculaire	178.300 g/mol
XLogP3	2.600
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	6
Exact Mass	177.994 Da
Monoisotopic Mass	177.994 Da
Topological Polar Surface Area	75.900 Å²
Heavy Atom Count	9
Formal Charge	0
Complexity	70.400
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

FAQ et articles

Diallyl Trisulfide

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

DATS DTS

Diallyl Trisulfide

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Allicin Diallyl Trisulfide Organosulfur Compound

Citations of This Product

How to Cite Aladdin Scientific Products? Citations Search

Calculateurs de solution

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Avis

📚 Citations by Application

Extraction & workup solvent2

Chromatography (HPLC / GC / TLC)2

Controlled-release & nanoparticle carrier2

Other applications1

Drug / compound screening1

View all 4 citations →

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Produits apparentés

Diallyl Trisulfide (DATS) - Moligand™, 10 mM in DMSO , CAS No.2050-87-5