Amidinothiourea

98%

Reagent Code: #123095
label
Alias Guanidinyl thiourea; Guanidine thiocyanate, 2-imino-4-sulfurized biuret
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CAS Number 2114-02-5

science Other reagents with same CAS 2114-02-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 118.16 g/mol
Formula C₂H₆N₄S
badge Registry Numbers
EC Number 218-308-0
MDL Number MFCD00014472
thermostat Physical Properties
Melting Point 171-173 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Amidinothiourea is primarily used in biochemical research as a reagent for studying enzyme inhibition, particularly in the context of understanding metabolic pathways. It acts as a competitive inhibitor for enzymes like arginase, which plays a role in the urea cycle, making it valuable for investigating nitrogen metabolism and related disorders. Additionally, it has been explored for its potential in synthesizing heterocyclic compounds, which are important in pharmaceutical development. Its ability to interact with metal ions also makes it useful in analytical chemistry for metal ion detection and separation processes.

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Test Parameter Specification
Melting Point 160-168
Purity (Nonaqueous Titration) 98-100
Appearance White Crystals

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿390.00
inventory 2.5kg
10-20 days ฿19,960.00
inventory 100g
10-20 days ฿880.00
inventory 500g
10-20 days ฿4,190.00

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Amidinothiourea
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Amidinothiourea is primarily used in biochemical research as a reagent for studying enzyme inhibition, particularly in the context of understanding metabolic pathways. It acts as a competitive inhibitor for enzymes like arginase, which plays a role in the urea cycle, making it valuable for investigating nitrogen metabolism and related disorders. Additionally, it has been explored for its potential in synthesizing heterocyclic compounds, which are important in pharmaceutical development. Its ability to in

Amidinothiourea is primarily used in biochemical research as a reagent for studying enzyme inhibition, particularly in the context of understanding metabolic pathways. It acts as a competitive inhibitor for enzymes like arginase, which plays a role in the urea cycle, making it valuable for investigating nitrogen metabolism and related disorders. Additionally, it has been explored for its potential in synthesizing heterocyclic compounds, which are important in pharmaceutical development. Its ability to interact with metal ions also makes it useful in analytical chemistry for metal ion detection and separation processes.

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