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Scopolamine methyl bromide

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Identification
Molecular formula
C17H23NO4Br
CAS number
155-41-9
IUPAC name
(1,1-dimethylpyrrolidin-1-ium-3-yl) 2-cyclopentyl-2-hydroxy-2-phenyl-acetate
State
State

At room temperature, scopolamine methyl bromide is in a solid state. It is a crystalline and somewhat hygroscopic solid, typically used under controlled conditions to prevent moisture absorption from the air.

Melting point (Celsius)
208.00
Melting point (Kelvin)
481.15
Boiling point (Celsius)
255.00
Boiling point (Kelvin)
528.15
General information
Molecular weight
394.32g/mol
Molar mass
394.3240g/mol
Density
1.2840g/cm3
Appearence

Scopolamine methyl bromide appears as a white crystalline powder. It is known for its strong hygroscopic nature, meaning it can easily absorb moisture from the environment. The powder is typically odorless or with a slight, characteristic odor.

Comment on solubility

Solubility of (1,1-dimethylpyrrolidin-1-ium-3-yl) 2-cyclopentyl-2-hydroxy-2-phenyl-acetate

The compound (1,1-dimethylpyrrolidin-1-ium-3-yl) 2-cyclopentyl-2-hydroxy-2-phenyl-acetate, with the chemical formula C17H23NO4Br, exhibits interesting solubility characteristics that can be categorized as follows:

  • Polarity: Due to the presence of both hydrophobic cyclopentyl and phenyl groups and hydrophilic hydroxyl and amine functional groups, solubility may vary significantly in different solvents.
  • Solvent Compatibility: This compound is likely to be soluble in polar solvents like water and alcohols, as well as in non-polar solvents such as chloroform or hexane due to its mixed functional group nature.
  • Temperature Dependence: Solubility may increase with temperature, a common trait observed in many organic compounds, maximizing its application potential in various formulations.
  • Concentration Effects: As the concentration increases, there may be a limit to solubility where precipitation occurs, especially in saturated solutions.

In summary, the *solubility* of this compound is influenced by a range of factors, determining its behavior in various environments. As a rule of thumb, the principle of "like dissolves like" often holds true in predicting its interactions. Understanding these parameters can aid in the effective utilization of (1,1-dimethylpyrrolidin-1-ium-3-yl) 2-cyclopentyl-2-hydroxy-2-phenyl-acetate in chemical applications.

Interesting facts

Interesting Facts About (1,1-Dimethylpyrrolidin-1-ium-3-yl) 2-Cyclopentyl-2-Hydroxy-2-Phenyl-Acetate

(1,1-Dimethylpyrrolidin-1-ium-3-yl) 2-cyclopentyl-2-hydroxy-2-phenyl-acetate is a fascinating compound that attracts attention due to its unique structure and potential applications. Here are some compelling aspects of this compound:

  • Structural Uniqueness: The presence of both a pyrrolidinium ring and multiple functional groups contributes to its interesting chemical behavior and reactivity.
  • Biological Relevance: Compounds similar to this one are often investigated for their pharmacological properties, making them potential candidates in medicinal chemistry for drug development.
  • Versatile Use: The ester functional group in its structure is known for its roles as a protective group in organic synthesis and is often utilized for creating advanced materials in polymer science.
  • Research Potential: As researchers explore the realms of chemical synthesis and materials science, such compounds may have applications in creating novel materials with unique properties.
  • Environmental Impact: Understanding the degradation pathways and biosafety of compounds like this is crucial, especially in fields such as environmental chemistry.

The compound showcases the beauty and complexity of organic chemistry, encouraging students and scientists alike to delve deeper into its properties and possible applications. "The study of compounds like this is where creativity meets scientific inquiry," as many chemists would affirm. As our understanding of such compounds expands, so does our ability to innovate solutions across various scientific disciplines.

Synonyms
Glycopyrronium
glycopyrronium bromide
13283-82-4
Glycopyrrolate ion
Glycopyrronium ion
Robinal
Glycopyrronium cation
(1,1-dimethylpyrrolidin-1-ium-3-yl) 2-cyclopentyl-2-hydroxy-2-phenylacetate
Glycopyrrolate cation
Seebri Neohaler
Tovanor Breezhaler
Glycopyrronium, erythro-
NCGC00179456-02
.beta.-1-Methyl-3-pyrrolidyl-.alpha.-cyclopentylmandelate methobromide
3-[(2-cyclopentyl-2-hydroxy-2-phenylacetyl)oxy]-1,1-dimethylpyrrolidin-1-ium
Prestwick0_000746
Prestwick1_000746
Prestwick2_000746
Prestwick3_000746
BSPBio_000732
SCHEMBL133002
SPBio_002671
BPBio1_000806
GTPL7459
CHEMBL1201335
DTXSID2048165
CHEBI:94449
ANGKOCUUWGHLCE-UHFFFAOYSA-N
Qbrexza&reg (glycopyrronium cloth)
BDBM50417445
Pyrrolidinium, 3-hydroxy-1,1-dimethyl-, bromide, .alpha.-cyclopentylmandelate
DB00986
MRF-0000310
NCGC00179456-01
SBI-0206947.P001
AB00513912
NS00008486
D10938
AB00513912-08
AB00513912_10
L001045
Q411917
BRD-A81233518-004-07-0
BRD-A81233518-004-16-1
3-(2-Cyclopentyl-2-hydroxy-2-phenylacetoxy)-1,1-dimethylpyrrolidin-1-ium
3-[(2-Cyclopentyl-2-hydroxy-2-phenylacetyl)oxy]-1,1-dimethylpyrrolidinium
(1,1-dimethylpyrrolidin-1-ium-3-yl) 2-cyclopentyl-2-hydroxy-2-phenyl-acetate
2-cyclopentyl-2-hydroxy-2-phenylacetic acid (1,1-dimethyl-3-pyrrolidin-1-iumyl) ester
Pyrrolidinium, 3-[(2-cyclopentyl-2-hydroxy-2-phenylacetyl)oxy]-1,1-dimethyl-