Diallyl Trisulfide (DATS) - Moligand™,≥65% , CAS No.2050-87-5

CAS: 2050-87-5 Cat. No.: D302734 Peso molecular: 178.34 Número EC: 218-107-8
Disponible para pedir
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥65%
Synonyms
CHEBI:78492 | EINECS 218-107-8 | Trisulfide, di-2-propenyl | Dasuansu | NSC 651936 | AS-75640 | Di-2-propenyl trisulfide | Trisulfide, di-2-propenyl (9CI) | DTXCID7025972 | HY-117235 | Diprop-2-en-1-yltrisulfane | CAS-2050-87-5 | FEMA 3265 | UBAXRAHSPKWNC
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
D302734-5g
3
29,90US$
25g
D302734-25g
2
99,90US$
100g
D302734-100g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
269,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

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

🌡

Storage & shipping

Store at -20°C,Argon charged Ships Ice chest + Ice pads 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 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Diallyl trisulfide, a constituent of garlic and onions, is a proapoptotic compound that also posesses antioxidant activity.

Diallyl trisulfide has been used to study its anti-carcinogenic properties in glioma and bladder cancer cell

Specifications

Sinónimos
CHEBI:78492 | EINECS 218-107-8 | Trisulfide, di-2-propenyl | Dasuansu | NSC 651936 | AS-75640 | Di-2-propenyl trisulfide | Trisulfide, di-2-propenyl (9CI) | DTXCID7025972 | HY-117235 | Diprop-2-en-1-yltrisulfane | CAS-2050-87-5 | FEMA 3265 | UBAXRAHSPKWNC
Especificaciones y pureza
Moligand™, ≥65%
Mecanismos bioquímicos y fisiológicos
Organosulphur compound. Increases glutathione S-transferase production (GST) and shows antimicrobial and chemoprotetive properties.
Condiciones de almacenamiento de almacenamiento
Store at -20°C, Argon charged
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Grado
Moligand™
Tipo de acción
INHIBITOR
Nota
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Pureza
≥65%
Nombres e identificadores
Sonrisas canónicasC=CCSSSCC=C
IUPAC Name3-(prop-2-enyltrisulfanyl)prop-1-ene
InChIKeyUBAXRAHSPKWNCX-UHFFFAOYSA-N
INCHI1S/C6H10S3/c1-3-5-7-9-8-6-4-2/h3-4H,1-2,5-6H2
Isómeros SMILES C=CCSSSCC=C
Peso molecular 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

KingdomOrganic compounds
SuperclassOrganosulfur compounds
ClaseOrganic trisulfides
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentOrganic trisulfides
Alternative Parents Allyl sulfur compounds  Sulfenyl compounds  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Organic trisulfide - Allyl sulfur compound - Sulfenyl compound - Hydrocarbon derivative - Aliphatic acyclic compound
DescripciónThis 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
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
TRPA1 Tclin Transient receptor potential cation channel subfamily A member 1 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
VDR Tclin Vitamin D receptor (26531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FASN Tchem Fatty acid synthase (3390 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GSR Tclin Glutathione reductase (335 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HPGD Tchem 15-hydroxyprostaglandin dehydrogenase [NAD+] (24926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HBA1 Tclin Hemoglobin HbA (880 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SCNN1A Tclin Amiloride-sensitive sodium channel, ENaC (10 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
MDCK (10148 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GCN5 Histone acetyltransferase GCN5 (89 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trpa1 Transient receptor potential cation channel subfamily A member 1 (1003 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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 NumberCertificate TypeFechaArticulo
C2618255Certificate of AnalysisMar 23, 2026 D302734
E2608335Certificate of AnalysisMar 07, 2026 D302734
E2608336Certificate of AnalysisMar 07, 2026 D302734
E2608337Certificate of AnalysisMar 07, 2026 D302734
F2129181Certificate of AnalysisApr 25, 2024 D302734
F2129183Certificate of AnalysisApr 25, 2024 D302734
K2419123Certificate of AnalysisApr 25, 2024 D302734
F2129182Certificate of AnalysisJul 05, 2021 D302734
J2323063Certificate of AnalysisJul 05, 2021 D302734
J2511117Certificate of AnalysisJul 05, 2021 D302734
Propiedades químicas y físicas
Peso molecular178.300 g/mol
XLogP32.600
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count3
Rotatable Bond Count6
Exact Mass177.994 Da
Monoisotopic Mass177.994 Da
Topological Polar Surface Area75.900 Ų
Heavy Atom Count9
Formal Charge0
Complexity70.400
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Pei Yu, Yini Yang, Jinyuan Sun, Xiao Jia, Chang Zheng, Qi Zhou, Fenghong Huang.  (2021)  Identification of volatile sulfur-containing compounds and the precursor of dimethyl sulfide in cold-pressed rapeseed oil by GC–SCD and UPLC–MS/MS.  FOOD CHEMISTRY,      [PMID:34399272] [10.1016/j.foodchem.2021.130741]
2. Liu Xin Chao, Zhou Ligang, Liu Qiyong, Liu Zhi Long.  (2015)  Laboratory Evaluation of Larvicidal Activity of the Essential oil of Allium tuberosum Roots and its Selected Major Constituent Compounds Against Aedes albopictus (Diptera: Culicidae).  JOURNAL OF MEDICAL ENTOMOLOGY,  52  (3): (437-441).  [PMID:26334818] [10.1093/jme/tjv016]
3. Jiang Mingzhou, Zhu Zhidong, Zhou Ziyu, Yan Zhiqiang, Huang Kai, Jiang Rongrong, Fan Xi, Jieensi Milayi, Pang Liewen, Wang Yiqing, Sun Xiaotian.  (2024)  A temperature-ultrasound sensitive nanoparticle delivery system for exploring central neuroinflammation mechanism in stroke-heart syndrome.  JOURNAL OF NANOBIOTECHNOLOGY,  22  (1): (1-19).  [PMID:39506743] [10.1186/s12951-024-02961-z]
4. Tingting Hu, Lu Jia, Heng Li, Chunyu Yang, Yuening Yan, Huiming Lin, Feng Zhang, Fengyu Qu, Wei Guo.  (2024)  An Intelligent and Soluble Microneedle Composed of Bi/BiVO4 Schottky Heterojunction for Tumor Ct Imaging and Starvation/Gas Therapy-Promoted Synergistic Cancer Treatment.  Advanced Healthcare Materials,      [PMID:38206853] [10.1002/adhm.202303147]
Calculadoras de soluciones
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