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Diphenyl diselenide - 96%, high purity , CAS No.1666-13-3

8 Citations COA COA
    Grade & Purity:
  • ≥96%
In stock
Item Number
D106407
Grouped product items
SKU Size
Availability
 Price Qty
D106407-5g
5g
3
$29.90
D106407-25g
25g
3
$86.90
D106407-100g
100g
2
$311.90
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View related series
Catalytic oxidation (1) Free radical initiators (1) Non heterocyclic block (8163) Selenium compounds (21)

Basic Description

Synonyms 1,2-Diphenyldiselane | Q3538196 | Diphenyl diselenide, 98% | 9ATU3Z459Q | DTXSID6061864 | 1,2-Diphenyldiselane # | A810750 | AC-11061 | InChI=1/C12H10Se2/c1-3-7-11(8-4-1)13-14-12-9-5-2-6-10-12/h1-10 | C12H10Se2 | NSC49763 | NSC-49763 | UNII-9ATU3Z459Q | D
Specifications & Purity ≥96%
Biochemical and Physiological Mechanisms Diphenyl diselenide inhibits δ-aminolevulinate dehydratase (δ-ALA-D) from brain, liver and kidney in vitro.
Storage Temp Argon charged
Shipped In Normal
Product Description

Diphenyl diselenide (Ph2Se2) is an organoselenium compound. Its crystalline structure, toxicokinetic properties,antioxidant and anti-inflammatory activities have been investigated. Its ability to reverse the oxidative brain damage and mitochondrial dysfunction induced by acetaminophen has been studied in mice. It reacts with thallium (Tl) to form TI (SePh). It participates in a four-component radical coupling to form substituted cyclopentanes.
Diphenyl diselenide inhibits δ-aminolevulinate dehydratase (δ-ALA-D) from brain, liver and kidney in vitro.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Benzene and substituted derivatives
Alternative Parents Organoselenium compounds  Hydrocarbon derivatives  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Monocyclic benzene moiety - Hydrocarbon derivative - Organoselenium compound - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
External Descriptors Not available

Associated Targets(Human)

EHMT2 Tchem Histone-lysine N-methyltransferase EHMT2 (1 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
EHMT1 Tchem Histone-lysine N-methyltransferase EHMT1 (1 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
HT-29 (80576 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SH-SY5Y (11521 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
EHMT1 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 5 (407 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Aspergillus (103 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Candida albicans (78123 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Fusarium (166 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name (phenyldiselanyl)benzene
INCHI InChI=1S/C12H10Se2/c1-3-7-11(8-4-1)13-14-12-9-5-2-6-10-12/h1-10H
InChIKey YWWZCHLUQSHMCL-UHFFFAOYSA-N
Smiles C1=CC=C(C=C1)[Se][Se]C2=CC=CC=C2
Isomeric SMILES C1=CC=C(C=C1)[Se][Se]C2=CC=CC=C2
WGK Germany 3
RTECS JM9152500
UN Number 3283
Molecular Weight 312.13
Beilstein 2047179
Reaxy-Rn 2047179
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2047179&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

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.

8 results found

Lot Number Certificate Type Date Item
H2125124 Certificate of Analysis Jun 09, 2025 D106407
H2125125 Certificate of Analysis Jun 09, 2025 D106407
H2125126 Certificate of Analysis Jun 09, 2025 D106407
L2004113 Certificate of Analysis Sep 06, 2024 D106407
B2512035 Certificate of Analysis Feb 17, 2022 D106407
E2207030 Certificate of Analysis Feb 17, 2022 D106407
E2207025 Certificate of Analysis Feb 17, 2022 D106407
E2207020 Certificate of Analysis Feb 17, 2022 D106407

Chemical and Physical Properties

Solubility Insoluble in water, soluble in toluene
Sensitivity Moisture &air sensitive
Boil Point(°C) 202°C/11mmHg
Melt Point(°C) 60-63°C
Molecular Weight 312.100 g/mol
XLogP3
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 0
Rotatable Bond Count 3
Exact Mass 313.911 Da
Monoisotopic Mass 313.911 Da
Topological Polar Surface Area 0.000 Ų
Heavy Atom Count 14
Formal Charge 0
Complexity 128.000
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

Solution Calculators

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