Interesting facts
Interesting Facts about 2-Carbamoyloxypropyl(trimethyl)ammonium Chloride
2-Carbamoyloxypropyl(trimethyl)ammonium chloride is a fascinating compound that exemplifies the intersection of organic chemistry and biochemistry. Here are some captivating aspects of this compound that make it noteworthy:
- Role in Biological Systems: Compounds with quaternary ammonium functional groups, such as this one, often play essential roles in biological systems, acting as surfactants and facilitating cellular processes.
- Applications in Industry: This compound may find applications in various industries ranging from pharmaceuticals to agrochemicals. Its unique structure allows it to interact effectively with biological membranes.
- Synthetic Versatility: The synthesis of 2-carbamoyloxypropyl(trimethyl)ammonium chloride showcases the versatility of organic synthetic methods. Scientists can employ various reaction pathways to create compounds with tailored functionalities.
- Research Properties: Researchers are continually investigating the physical and chemical properties of compounds like this to develop new applications, particularly in drug delivery systems and antimicrobial agents.
- Potential in Green Chemistry: The development and use of compounds such as this aligns with the principles of green chemistry, emphasizing the need for sustainable practices in chemical manufacturing.
As a compound, 2-carbamoyloxypropyl(trimethyl)ammonium chloride not only represents a unique blend of chemistry but also highlights the ongoing innovations within the scientific community. As we derive further understanding from its properties and applications, it can lead to exciting advancements in multiple fields.
Synonyms
Bethanechol chloride
590-63-6
Besacholine
Mechothane
Mechotane
Mecothane
Mictone
Uro-Carb
Urecholine chloride
Muscaran
Carbamylmethylcholine chloride
Bethaine choline chloride
Trimethyl(2-carbamoyloxypropyl)ammonium chloride
beta-Methyl carbachol chloride
(2-Hydroxypropyl)trimethylammonium chloride carbamate
2-(carbamoyloxy)-N,N,N-trimethylpropan-1-aminium chloride
beta-Methylcholine chloride urethan
UNII-H4QBZ2LO84
EINECS 209-686-8
H4QBZ2LO84
NSC 30783
NSC-30783
Carbaminoyl, beta-methylcholine chloride
CHEBI:3085
2-((Aminocarbonyl)oxy)-N,N,N-trimethyl-1-propanaminium chloride
DTXSID2022676
1-Propanaminium, 2-[(aminocarbonyl)oxy]-N,N,N-trimethyl-, chloride
DTXCID902676
1-Propanaminium, 2-((aminocarbonyl)oxy)-N,N,N-trimethyl-, chloride
NSC30783
Bethanechol chloride [USP:BAN:JAN]
AMMONIUM, (2-HYDROXYPROPYL)TRIMETHYL-, CHLORIDE, CARBAMATE
BETHANECHOL CHLORIDE (MART.)
BETHANECHOL CHLORIDE [MART.]
BETHANECHOL CHLORIDE (USP-RS)
Bethanechol chloride (USP:BAN:JAN)
BETHANECHOL CHLORIDE [USP-RS]
BETHANECHOL CHLORIDE (USP MONOGRAPH)
BETHANECHOL CHLORIDE [USP MONOGRAPH]
Chloride, Bethanechol
Bethanechol Chloride 5 mg
Bethanechol Chloride 10 mg
Bethanechol Chloride 25 mg
Bethanechol Chloride 50 mg
(+-)-(2-Hydroxypropyl)trimethylammonium chloride carbamate
1-Propanaminium, 2-((aminocarbonyl)oxy)-N,N,N-trimethyl-, chloride, (+-)-
(2RS)-2-Carbamoyloxy-N,N,N-trimethylpropylaminium chloride
209-686-8
Urecholine
Duvoid
Myocholine
Myotonachol
Mictrol
Bethanechol (chloride)
Carbamyl-beta-methylcholine chloride
2-Carbamoyloxypropyltrimethylammonium chloride
2-(Carbamoyloxy)-N,N,N-trimethyl-1-propanaminium Chloride
MLS000028675
Myotonine
MFCD00055224
SMR000058680
(2-Carbamoyloxypropyl)trimethylammonium chloride
2-carbamoyloxypropyl(trimethyl)azanium;chloride
(+/-)-(2-HYDROXYPROPYL)TRIMETHYLAMMONIUM CHLORIDE CARBAMATE
Myotonine chloride
1-PROPANAMINIUM, 2-((AMINOCARBONYL)OXY)-N,N,N-TRIMETHYL-, CHLORIDE, (+/-)-
SR-01000000282
NCGC00163217-01
carbamyl-|A-methylcholine chloride
Urecholine (TN)
regid855684
Opera_ID_1125
CAS-590-63-6
CHEMBL1768
SCHEMBL37393
Ammonium, chloride, carbamate
MLS001148071
MLS006011984
SPECTRUM1500146
Carbamyl--methylcholine chloride
.beta.-Methyl carbachol chloride
HMS500I21
HY-B0406A
BETHANECHOL CHLORIDE [MI]
Carbamyl-ss-methylcholine chloride
Bethanechol chloride (JP18/USP)
BETHANECHOL CHLORIDE [JAN]
HMS1571G08
HMS1920G19
HMS2091M19
HMS2098G08
HMS2232D09
HMS3259L15
HMS3260N10
HMS3374D01
HMS3656G21
HMS3715G08
HMS3884H19
Pharmakon1600-01500146
BETHANECHOL CHLORIDE [VANDF]
Tox21_112028
Tox21_500304
CCG-38936
NSC755913
s2455
.beta.-Methylcholine chloride urethan
BETHANECHOL CHLORIDE [WHO-DD]
AKOS006230324
Carbamyl- beta -methylcholine chloride
Tox21_112028_1
Carbamyl-beta-methylcholine chloride.cd
FB16196
LP00304
NC00660
NSC-755913
NCGC00015245-10
NCGC00093753-01
NCGC00093753-02
NCGC00093753-03
NCGC00093753-04
NCGC00093753-05
NCGC00260989-01
AS-13371
BETHANECHOL CHLORIDE [ORANGE BOOK]
Carbaminoyl, .beta.-methylcholine chloride
WLN: ZVOY1&1K1&1&1 &Q &G
B4828
EU-0100304
NS00080176
SW197254-3
EN300-51035
C 5259
C08202
D01000
F20466
A832139
1-(trimethylazaniumyl)propan-2-yl carbamate chloride
SR-01000000282-2
SR-01000000282-4
SR-01000000282-7
Q27105939
2-[(aminocarbonyl)oxy]-N,N,N-trimethylpropan-1-aminium chloride
1-Propanaminium, 2-((aminocarbonyl)oxy)-N,N,N-trimethyl-, chloride (1:1)
2-carbamoyloxypropyl(trimethyl)ammonium chloride;2-(Carbamoyloxy)-N,N,N-trimethyl-1-propanaminium Chloride
Solubility of 2-carbamoyloxypropyl(trimethyl)ammonium chloride
The solubility of 2-carbamoyloxypropyl(trimethyl)ammonium chloride is influenced by several key factors:
In summary, this compound is likely to exhibit good solubility in aqueous solutions owing to its ionic character and the ability to engage in strong intermolecular interactions. As with many ammonium compounds, solubility can vary under different conditions, such as temperature and the presence of other solutes, highlighting the importance of context in solubility studies.