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AB49609

213764-25-1 | Cyclopropylhydrazine hydrochloride

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $10.00 $7.00 -   +
1g 97% in stock $15.00 $11.00 -   +
5g 97% in stock $68.00 $48.00 -   +
10g 97% in stock $130.00 $91.00 -   +
25g 97% in stock $325.00 $228.00 -   +

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*All prices are in USD.

Description
Catalog Number: AB49609
Chemical Name: Cyclopropylhydrazine hydrochloride
CAS Number: 213764-25-1
Molecular Formula: C3H9ClN2
Molecular Weight: 108.57
MDL Number: MFCD16658753
SMILES: NNC1CC1.Cl

 

Computed Properties
Complexity: 31.9  
Covalently-Bonded Unit Count: 2  
Heavy Atom Count: 6  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 3  
Rotatable Bond Count: 1  

 

 

Upstream Synthesis Route
  • The upstream synthesis route of cyclopropylhydrazine hydrochloride starts with the formation of cyclopropyl bromide. This is typically achieved by treating cyclopropyl alcohol with hydrobromic acid (HBr), resulting in a substitution reaction that replaces the hydroxyl group with a bromine atom, creating the alkyl bromide intermediate.
    
    The next step involves the generation of hydrazine. Industrially, this is often done through the Raschig process, which involves the oxidation of ammonia with sodium hypochlorite in the presence of a gelatin or glue promoter. Alternatively, the Olin Raschig process can be used, where ammonia reacts with sodium hypochlorite at higher temperatures without a promoter, to give chloramine, which is subsequently reacted with ammonia to form hydrazine.
    
    Once hydrazine is available, it can be reacted with cyclopropyl bromide to form cyclopropylhydrazine via nucleophilic substitution of the bromide with the nitrogen of the hydrazine molecule. This reaction usually requires the presence of a base to deprotonate the hydrazine, making it a better nucleophile.
    
    Finally, the free base cyclopropylhydrazine is treated with hydrochloric acid to yield the cyclopropylhydrazine hydrochloride salt. The formation of the hydrochloride salt enhances the solubility of cyclopropylhydrazine in water and often improves its stability, making it easier to handle and store.
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