Azetidine hydrochloride

Modify Date: 2025-08-25 15:11:45

Azetidine hydrochloride Structure
Azetidine hydrochloride structure
Common Name Azetidine hydrochloride
CAS Number 36520-39-5 Molecular Weight 93.56
Density N/A Boiling Point 103.8ºC at 760 mmHg
Molecular Formula C3H8ClN Melting Point >300 °C(lit.)
MSDS Chinese USA Flash Point 152 °C
Symbol GHS07
GHS07
Signal Word Warning

 Use of Azetidine hydrochloride


Azetidine hydrochloride is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

 Names

Name Azetidine hydrochloride
Synonym More Synonyms

 Azetidine hydrochloride Biological Activity

Description Azetidine hydrochloride is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related Catalog

 Chemical & Physical Properties

Boiling Point 103.8ºC at 760 mmHg
Melting Point >300 °C(lit.)
Molecular Formula C3H8ClN
Molecular Weight 93.56
Flash Point 152 °C
Exact Mass 93.034531
PSA 12.03000
LogP 1.11050
InChIKey HGQULGDOROIPJN-UHFFFAOYSA-N
SMILES C1CNC1.Cl
Storage condition Room temperature.

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305 + P351 + P338
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xi:Irritant;
Risk Phrases R36/37/38
Safety Phrases S26
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2933990090

 Customs

HS Code 2933990090
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Articles4

More Articles
Practical syntheses of N-substituted 3-hydroxyazetidines and 4-hydroxypiperidines by hydroxylation with Sphingomonas sp. HXN-200.

Org. Lett. 4 , 1859-1862, (2002)

[reaction: see text] Hydroxylation of N-substituted azetidines 11 and 12 and piperidines 15-19 with Sphingomonas sp. HXN-200 gave 91-98% of the corresponding 3-hydroxyazetidines 13 and 14 and 4-hydrox...

Domino formation of enamines--intramolecular cyclizations to 1-aminotetralins from γ-arylallene aldehydes and amines.

Org. Lett. 16(20) , 5438-41, (2014)

1,5-/1,6-Allenals conjugated to an aromatic ring undergo a cyclization, in the presence of an amine, that leads to tricyclic compounds including the 1-aminotetralin scaffold. This domino process combi...

Synthesis and biological evaluation of a novel phenyl substituted sydnone series as potential antitumor agents.

Bioorg. Med. Chem. Lett. 13 , 2899-2901, (2003)

A series of compounds containing an N-(4'-substituted-3'-nitrophenyl)sydnone moiety with potential antitumor activity was prepared based on active analogues. The rationale behind the design of these c...

 Synonyms

Azetidine, hydrochloride (1:1)
azetadine hydrochloride
Azetidinhydrochlorid
AZETIDINE HCL
azetidine monohydrochloride
Azacyclobutane Hydrochloride
Azetidine hydrochloride (1:1)
TRIMETHYLENEIMINE HYDROCHLORIDE
azetidinium chloride
hydrochloride salt of azetidine
azetidine HCl salt
EINECS 207-963-8
TriMethyleniMine Hydrochloride
MFCD00191762
1,3-PropyleniMine Hydrochloride
Tetrahydro-azete Hydrochloride
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