4910-62-7

Basic information

• Product Name: AzodicarboxaMide DipotassiuM Salt
• Synonyms: AzodicarboxaMide DipotassiuM Salt
• CAS NO: 4910-62-7
• Molecular Formula: C₂N₂O₄*2K
• Molecular Weight: 194.229
• Product Categories: Amines, Miscellaneous Reagents
• Mol File: 4910-62-7.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 357.1°Cat760mmHg
• Flash Point: 169.8°C
• Appearance: /
• Density: 1.87g/cm³
• Vapor Pressure: 4.59E-06mmHg at 25°C
• Refractive Index: 1.591
• CAS DataBase Reference: AzodicarboxaMide DipotassiuM Salt(CAS DataBase Reference)
• NIST Chemistry Reference: AzodicarboxaMide DipotassiuM Salt(4910-62-7)
• EPA Substance Registry System: AzodicarboxaMide DipotassiuM Salt(4910-62-7)

Safety Data

• Hazardous Substances Data: 4910-62-7(Hazardous Substances Data)

Usage

Uses

Azodicarboxamide Dipotassium Salt is a derivative of Azodicarboxamide (A941000). It is used as an additive to wheat flour breads to improve the physical properties of the dough. It is also used to optimize the levels of oxidant/reducing agents in the baking of wheat flour.

InChI:InChI=1/C2H2N2O4/c5-1(6)3-4-2(7)8/h(H,5,6)(H,7,8)/b4-3+

Upstream product

• 123-77-3 Azodicarboxamid 

Downstream Products

• 13762-95-3 deuterated hydrazine hydrate 
• 1211323-74-8 (3S,4R,8S,10S,12S,14S)-3-(benzyloxy)-14-((R,Z)-4-(benzyloxymethyl)hex-2-en-2-yl)-8,10-dihydroxy-4,12-dimethoxy-9,9-dimethyl-1-oxacyclotetradecan-2-one 
• 124-38-9 carbon dioxide 
• 7727-37-9 nitrogen 
• 302-01-2 hydrazine 
• 245073-91-0 [(Ru(P(C₆H₁₁)3)(C₁₄H₁₂S₄))2NHNH] 

Relevant articles and documents

Biogenesis-Guided Synthesis and Structural Revision of Sarocladione Enabled by Ruthenium-Catalyzed Endoperoxide Fragmentation

Sarocladione is the first 5,10:8,9-diseco-steroid with a 14-membered macrocyclic diketone framework to have been isolated from a natural source. Herein we report a biomimetic synthesis of sarocladione in only two or seven steps from inexpensive, commercially available ergosterol. The key feature of this synthesis was a novel ruthenium-catalyzed endoperoxide fragmentation, which transformed various saturated endoperoxides into olefinic diketones by cleavage of two C?C bonds. This synthesis allowed us to unambiguously determine the structure of sarocladione and provided experimental support for its revised biosynthetic origin. This work also vividly demonstrates that consideration of the biogenesis is a powerful tool for elucidating the structures of natural products.

Light-Stabilized Dynamic Materials

The light-responsive adaptation of polymer materials typically requires different wavelengths or additional heat to induce reversible covalent bond formation and dissociation. Here, we bypass the use of invasive triggers by introducing light-stabilized dynamic materials that can undergo a repeatable change in topology from a covalently cross-linked material into a liquid polymer formulation by switching one visible light source on-and-off without the need for any additional triggers. Specifically, we exploit the photo-Diels-Alder reaction of triazolinediones with naphthalenes as a dynamic covalent cross-linking platform that enables green light-induced network formation, while the cross-linked material collapses through spontaneous cycloreversion upon standing in the dark at ambient temperature. Importantly, the covalent cross-links remain stabilized for as long as visible light is present, thereby retaining the material's structural integrity. This enables their potential use in an array of light-directed applications whereby network properties such as stiffness can be tuned by the mildest trigger of all: darkness.

Cinnamic acid derivatives as inhibitors for chorismatases and isochorismatases

Chorismatases and isochorismatases catalyse the hydrolysis of chorismate or isochorismate leading to unsaturated cyclohexenoic acid derivatives. Based on simplification of the physiological substrates, two cinnamic acid-derived compounds, differing in the