Bathocuproinedisulfonic acid disodiuM salt hydrate

Product Name: Bathocuproinedisulfonic acid disodiuM salt hydrate
CAS No.: 1257642-74-2
Chemical Name: Bathocuproinedisulfonic acid disodiuM salt hydrate
Synonyms: BATHOCUPROIN SULFONATE HYDRATE;BATHOCUPROIN SULFONATE DISODIUM SALT HYDRATE;BATHOCUPROINDISULFONIC ACID DISODIUM SALT HYDRATE;BATHOCUPROINEDISULFONIC ACID, DISODIUM SALT HYDRATE;Bathocuproinedisulfonic acid hydrate disodium salt;Sodium 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline-3,8-disulfonate hydrate;2,9-DIMETHYL-4,7-DIPHENYL-1,10-PHENANTHROLINEDISULFONIC ACID, DISODIUM SALT HYDRATE;Sodium 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline-3,8-disulfonate hydrate (2:1:1)
CBNumber: CB6286233
Molecular Formula: C26H23N2NaO7S2
Formula Weight: 562.59
MOL File: Mol file

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Bathocuproinedisulfonic acid disodiuM salt hydrate Property

Melting point:: 300 °C(lit.)

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Safety

Safety Statements: 22-24/25
WGK Germany: 3

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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 146625
Product name: Bathocuproinedisulfonic acid disodium salt hydrate
Packaging: 1g
Price: $133
Updated: 2023/01/07

Sigma-Aldrich

Product number: 146625
Product name: Bathocuproinedisulfonic acid disodium salt hydrate
Packaging: 5g
Price: $638
Updated: 2023/01/07

American Custom Chemicals Corporation

Product number: EMT0000039
Product name: BATHOCUPROIN SULFONATE DISODIUM SALT HYDRATE
Purity: 95.00%
Packaging: 5MG
Price: $497.88
Updated: 2021/12/16

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Bathocuproinedisulfonic acid disodiuM salt hydrate Chemical Properties,Usage,Production

Uses

Bathocuproinedisulfonic acid disodium salt hydrate was used as chelator in electron spin resonance spin trapping technique to study free radical generation in rats with acute sodium formate poisoning. It was used as reagent for determination of Cu and Cu-protein complexes.

Uses

Bathocuproinedisulfonic acid disodiuM salt hydrate cna be usd as reagent used for determination of Cu1 and Cu-protein complexes.2

General Description

Bathocuproine disulfonic acid (BCDS) is a stable Cu⁺ chelator and BCDS-Cu⁺ inhibits the HIV-1 wild type protease as well as a mutant HIV-1 protease lacking cysteine. It is an extracellular copper chelator.

Bathocuproinedisulfonic acid disodiuM salt hydrate Preparation Products And Raw materials

Raw materials

Preparation Products

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Bathocuproinedisulfonic acid disodiuM salt hydrate Suppliers

China 25 Germany 1 Japan 1 Switzerland 1 United States 2 Global 30

Tianjin Derchemist Science & Technology Co., Ltd.

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Shanghai Aladdin Bio-Chem Technology Co.,LTD

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Shanghai Macklin Biochemical Co.,Ltd.

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Country: China
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Sigma-Aldrich

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Aikon International Limited

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Shanghai Anyinuo Biomedical Technology Co., Ltd.

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Hebei Mojin Biotechnology Co., Ltd

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Henan Weituxi Chemical Technology Co., Ltd.

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Hebei Weibang Biotechnology Co., Ltd

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Guangdong Wengjiang Chemical Reagent Co., Ltd.

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View Lastest Price from Bathocuproinedisulfonic acid disodiuM salt hydrate manufacturers

Hebei Weibang Biotechnology Co., Ltd

Product: Bathocuproinedisulfonic acid disodiuM salt hydrate 1257642-74-2
Price: US $0.00/KG
Min. Order: 1KG
Purity: 99%
Supply Ability: 100 mt
Release date: 2024-11-07

Henan Bao Enluo International TradeCo.，LTD

Product: Bathocuproinedisulfonic acid disodiuM salt hydrate 1257642-74-2
Price: US $50.00/kg
Min. Order: 1kg
Purity: 99.9%
Supply Ability: 10000MT
Release date: 2023-08-15

Hebei Mojin Biotechnology Co., Ltd

Product: Bathocuproinedisulfonic acid disodiuM salt hydrate 1257642-74-2
Price: US $60.00/KG
Min. Order: 25KG
Purity: 99.99%
Supply Ability: 200ton
Release date: 2023-07-27

1257642-74-2, Bathocuproinedisulfonic acid disodiuM salt hydrateRelated Search:

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Bathocuproinedisulfonic acid hydrate disodium salt

Sodium 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline-3,8-disulfonate hydrate (2:1:1)

Sodium 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline-3,8-disulfonate hydrate

1257642-74-2

Building Blocks

Chemical Synthesis

Organic Building Blocks

Sulfonic/Sulfinic Acid Salts

Sulfur Compounds

Organic Building Blocks

Sulfonic/Sulfinic Acid Salts

Sulfur Compounds