20240-62-4 Usage
Chemical classification
Hydrazine derivative It is a compound derived from hydrazine (N2H4) with two alkyl substituents.
Alkyl substituents
1-methyl and 2-n-butyl The two alkyl groups attached to the hydrazine molecule are a methyl group (CH3) and a n-butyl group (CH3CH2CH2CH2-).
Usage
Rocket propellant fuel 1-Methyl-2-n-butylhydrazine is commonly used as a fuel in rocket propulsion systems.
Flammability
Highly flammable The compound can easily catch fire and burn, posing a significant risk.
Toxicity
Toxic to humans and the environment Exposure to 1-Methyl-2-n-butylhydrazine can cause harm to both living organisms and ecosystems.
Reducing agent
Strong reducing agent The compound is capable of donating electrons to other substances, making it a powerful reducing agent.
Reactivity with oxidizing agents
Reacts vigorously 1-Methyl-2-n-butylhydrazine can react intensely with substances that are oxidizing agents, potentially causing hazardous situations.
Natural occurrence
Not naturally occurring The compound is not found in nature and is produced synthetically for industrial purposes.
Precautions
Handling and storage safety Due to its potential hazards, care must be taken when working with 1-Methyl-2-n-butylhydrazine to prevent accidents and minimize risks.
Check Digit Verification of cas no
The CAS Registry Mumber 20240-62-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,2,4 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20240-62:
(7*2)+(6*0)+(5*2)+(4*4)+(3*0)+(2*6)+(1*2)=54
54 % 10 = 4
So 20240-62-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H14N2/c1-3-4-5-7(2)6/h3-6H2,1-2H3
20240-62-4Relevant articles and documents
Amidrazones 13. A Convenient Method for the Preparation of 1-Alkyl-1-methylhydrazines
Smith, Richard F.,Brophy, Keith A.,Rodriguez, George,Dennis, Lisa A.,Ryan, William J.
, p. 183 - 188 (2007/10/02)
An efficient one-pot procedure for the preparation of 1-alkyl-1-methylhydrazines from methylhydrazine via base-promoted hydrolysis of 1-alkyl-3-amino-4,5-dihydro-1-methyl-1H-pyrazolium halides (3) is described.
