Skip to main content

2-Benzyl-4,5-dihydro-1H-imidazole hydrochloride

ADVERTISEMENT
Identification
Molecular formula
C10H14N2HCl
CAS number
61536-70-7
IUPAC name
2-benzyl-4,5-dihydro-1H-imidazole;hydrochloride
State
State

At room temperature, the compound is a solid. It is stable under recommended storage conditions, which should be dry and well-ventilated areas.

Melting point (Celsius)
238.00
Melting point (Kelvin)
511.15
Boiling point (Celsius)
245.30
Boiling point (Kelvin)
518.40
General information
Molecular weight
195.23g/mol
Molar mass
195.2330g/mol
Density
1.2200g/cm3
Appearence

2-Benzyl-4,5-dihydro-1H-imidazole hydrochloride typically appears as a white to off-white crystalline powder. It is hygroscopic and should be stored in a tightly closed container to prevent moisture absorption.

Comment on solubility

Solubility of 2-benzyl-4,5-dihydro-1H-imidazole;hydrochloride

The solubility of 2-benzyl-4,5-dihydro-1H-imidazole hydrochloride (C10H14N2HCl) showcases some intriguing characteristics:

  • Solvent Dependence: This compound is typically soluble in polar solvents, such as water and methanol, due to the presence of the hydrochloride, which enhances its hydrophilicity.
  • Temperature Effect: Like many organic compounds, its solubility can vary with temperature; generally, an increase in temperature leads to increased solubility.
  • pH Influence: The solubility may also be affected by the pH of the solution. As a salt, it is more soluble in acidic conditions where it remains in its ionic form.
  • Crystallization: If prepared correctly, it can crystallize from solutions, which indicates a balance between solubility and solid-state stability.

To conclude, the solubility of 2-benzyl-4,5-dihydro-1H-imidazole hydrochloride reflects the interplay between its chemical structure and the solvent environment, allowing for various applications in pharmaceuticals and research.

Interesting facts

Interesting Facts about 2-benzyl-4,5-dihydro-1H-imidazole; hydrochloride

The compound 2-benzyl-4,5-dihydro-1H-imidazole; hydrochloride is a fascinating member of the imidazole family, showcasing unique properties and potential applications in various fields. Here are some notable aspects to understand:

  • Pharmaceutical Relevance: This compound, related to the imidazole structure, often plays a role in pharmaceuticals, contributing to the development of several therapeutic agents.
  • Biochemical Interactions: Due to the presence of the imidazole ring, it may participate in numerous biochemical interactions, particularly in the context of enzyme function and ligand-receptor binding.
  • Substituent Influence: The benzyl group enhances stability and solubility, making this compound attractive for drug design, where molecular modifications can lead to increased activity or selectivity.
  • Analytical Applications: Its unique structure allows it to serve as a standard for various analytical techniques, aiding in the assessment of related compounds.

Furthermore, ikiștiu aupодоs ado dокерفا gmind a largi потомxer cardioges (corednemo rиза team).

To sum up, 2-benzyl-4,5-dihydro-1H-imidazole; hydrochloride is not just a simple compound but rather a gateway to deeper research opportunities and a better understanding of imidazole chemistry. As researchers continue to explore its potential, we could see exciting developments in the fields of medicinal chemistry and pharmacology.

Synonyms
Tolazoline hydrochloride
59-97-2
Tolazoline HCl
2-benzyl-4,5-dihydro-1H-imidazole hydrochloride
Priscoline
2-Benzyl-2-imidazoline hydrochloride
Arterodyl
Tolavad
Tolpal
Priscoline hydrochloride
Benzazoline hydrochloride
Tolazoline chloride
Tolazoline (hydrochloride)
Imidaline hydrochloride
Benzylimidazoline hydrochloride
1H-Imidazole, 4,5-dihydro-2-(phenylmethyl)-, monohydrochloride
2-Benzyl-2-imidazoline monohydrochloride
2-Imidazoline, 2-benzyl-, hydrochloride
AI3-52042
EINECS 200-447-3
UNII-E669Z6S1JG
NSC-757353
E669Z6S1JG
DTXSID9021718
TCMDC-125842
Cloridrato di 2-benzil-4,5-imidazolina
MLS000559484
DTXCID001718
4,5-Dihydro-2-(phenylmethyl)-1H-imidazole monohydrochloride
2-IMIDAZOLINE, 2-BENZYL-, MONOHYDROCHLORIDE
Tolazoline hydrochloride [USP:JAN]
NSC 757353
SMR000149600
1H-Imidazole, 4,5-dihydro-2-(phenylmethyl)-, hydrochloride (1:1)
Imidaline (hydrochloride); NSC35110 (hydrochloride)
2-benzyl-4,5-dihydro-1H-imidazole;hydrochloride
Tolazoline hydrochloride (USP:JAN)
TOLAZOLINE HYDROCHLORIDE (MART.)
TOLAZOLINE HYDROCHLORIDE [MART.]
TOLAZOLINE HYDROCHLORIDE (USP-RS)
TOLAZOLINE HYDROCHLORIDE [USP-RS]
Tolazoline hydrochloride [JAN]
TOLAZOLINE HYDROCHLORIDE (USP MONOGRAPH)
TOLAZOLINE HYDROCHLORIDE [USP MONOGRAPH]
CAS-59-97-2
NCGC00016271-01
MFCD00012693
SR-01000665661
Tolazine Injection
Priscoline (TN)
Cloridrato di 2-benzil-4,5-imidazolina [Italian]
Prestwick_770
2-BENZYL-2-IMIDAZOLINEHYDROCHLORIDE
Opera_ID_1028
Tolazoline Monohydrochloride
CHEMBL1689
2-Benzyl-2-imidazoline HCl
SCHEMBL34869
Tolazoline Hydrochloride,(S)
SPECTRUM1500580
CHEBI:9615
HY-A0066AR
2-(phenylmethyl)-4,5-dihydro-1H-imidazole hydrochloride
HY-A0066A
RHTNTTODYGNRSP-UHFFFAOYSA-N
HMS1568K21
HMS1921E17
Pharmakon1600-01500580
Tolazoline hydrochloride (JAN/USP)
Tox21_110339
CCG-39122
NSC757353
s4124
TOLAZOLINE HYDROCHLORIDE [MI]
AKOS015900184
AKOS028109640
Tolazoline (hydrochloride) (Standard)
Tox21_110339_1
CS-4287
KS-5261
NC00612
TOLAZOLINE HYDROCHLORIDE [VANDF]
NCGC00016271-05
NCGC00094795-01
NCGC00094795-02
TOLAZOLINE HYDROCHLORIDE [WHO-DD]
DB-014037
NS00078966
SW196909-3
T3791
TOLAZOLINE HYDROCHLORIDE [GREEN BOOK]
TOLAZOLINE HYDROCHLORIDE [ORANGE BOOK]
D00997
E77029
EN300-119526
Imidaline hydrochloride;Benzidazol hydrochloride
SR-01000665661-3
Q27276930
Z1255415487
2-Benzyl-2-imidazoline hydrochloride,2-Benzyl-2-imidazoline
Tolazoline Hydrochloride 1.0 mg/ml in Methanol (as free base)
Tolazoline hydrochloride, United States Pharmacopeia (USP) Reference Standard
200-447-3