2,2'-Dithiodibenzoic acid

98%

Reagent Code: #169562
label
Alias 2, 2’-Dithiodibenzoic acid (DTSA); dithiosalicylic acid, DTSA, 2, 2’-Dithiodibenzoic acid
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CAS Number 119-80-2

science Other reagents with same CAS 119-80-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 306.36 g/mol
Formula C₁₄H₁₀O₄S₂
badge Registry Numbers
EC Number 204-352-8
MDL Number MFCD00002465
thermostat Physical Properties
Melting Point 287-290 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of drugs that require disulfide linkages for biological activity. Plays a role in the development of radiopharmaceuticals due to its ability to chelate metals and form stable complexes. Employed in biochemical research for modifying proteins and peptides by introducing disulfide bridges, aiding in structure-function studies. Also utilized in the preparation of functionalized surfaces and biosensors, where its disulfide bond enables reversible binding and self-assembled monolayer formation on gold surfaces. Shows utility in polymer chemistry as a crosslinking agent to enhance mechanical and thermal properties of materials.

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Test Parameter Specification
Melting Point 287-292°C
Purity (HPLC) (%) 97.5-100%
Appearance Off-white to yellow to grey to brown powder or crystals
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿360.00
inventory 500g
10-20 days ฿2,060.00
inventory 2.5kg
10-20 days ฿8,980.00
inventory 100g
10-20 days ฿860.00

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2,2'-Dithiodibenzoic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of drugs that require disulfide linkages for biological activity. Plays a role in the development of radiopharmaceuticals due to its ability to chelate metals and form stable complexes. Employed in biochemical research for modifying proteins and peptides by introducing disulfide bridges, aiding in structure-function studies. Also utilized in the preparation of functionalized surfaces and biosensors, where its disulfide bond enables reversible binding and self-assembled monolayer formation on gold surfaces. Shows utility in polymer chemistry as a crosslinking agent to enhance mechanical and thermal properties of materials.
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