Skip to main content

Carisoprodol hydrochloride

ADVERTISEMENT
Identification
Molecular formula
C12H16ClNO3
CAS number
673-37-2
IUPAC name
2-(dimethylamino)ethyl 2-(4-chlorophenoxy)acetate;hydrochloride
State
State

At room temperature, 2-(dimethylamino)ethyl 2-(4-chlorophenoxy)acetate;hydrochloride is typically a solid.

Melting point (Celsius)
65.50
Melting point (Kelvin)
338.70
Boiling point (Celsius)
285.10
Boiling point (Kelvin)
558.20
General information
Molecular weight
305.22g/mol
Molar mass
305.2180g/mol
Density
1.1100g/cm3
Appearence

2-(Dimethylamino)ethyl 2-(4-chlorophenoxy)acetate;hydrochloride appears as a white to off-white powder. It may form crystalline structures depending on the purification process and storage conditions.

Comment on solubility

Solubility of 2-(dimethylamino)ethyl 2-(4-chlorophenoxy)acetate; hydrochloride

The compound known as 2-(dimethylamino)ethyl 2-(4-chlorophenoxy)acetate; hydrochloride exhibits notable solubility characteristics due to its ionic and polar nature. Here are some key points regarding its solubility:

  • Solvent Compatibility: This compound tends to be soluble in water and various organic solvents, thanks to the presence of the hydrochloride moiety which increases its affinity for polar environments.
  • Temperature Influence: As with many salts, an increase in temperature can enhance its solubility. Higher temperatures generally facilitate the dissolution process.
  • pH Dependence: The solubility can also vary with pH levels; typically, in more acidic conditions, the solubility may be greater because the hydrochloride form is stable.
  • Formation of Solutions: When dissolved in water, this compound can dissociate into ions, creating an environment conducive to biological activity.

Overall, 2-(dimethylamino)ethyl 2-(4-chlorophenoxy)acetate; hydrochloride showcases interactive solubility traits that can be harnessed for various applications, particularly in pharmaceutical formulations. Understanding its solubility behavior aids in predicting its bioavailability and effectiveness in biological systems.

Interesting facts

Interesting Facts about 2-(Dimethylamino)ethyl 2-(4-chlorophenoxy)acetate; Hydrochloride

This compound, often referred to by its abbreviated name, showcases the intriguing interplay between chemical structure and biological activity. Here are some fascinating insights:

  • Pharmaceutical Relevance: 2-(Dimethylamino)ethyl 2-(4-chlorophenoxy)acetate; hydrochloride is considered a significant building block in the pharmaceutical industry, especially in the development of drugs targeting neurological and vascular conditions.
  • Ester Derivative: This compound is part of a broader class of compounds known as esters, which are typically formed from the reaction of an acid with an alcohol. Its ester bond plays a crucial role in both chemical stability and reactivity.
  • Mechanism of Action: The unique structure of this compound allows it to interact with specific receptors in the body, potentially influencing neurotransmitter levels and vascular responses. This property makes it a valuable subject of study in pharmacology.
  • Structural Features: The presence of a dimethylamino group enhances its lipophilicity, allowing for better membrane permeability. Meanwhile, the chlorophenoxy group contributes to its binding affinity, which is pivotal in drug efficacy.
  • Synthesis Techniques: The synthesis of this compound involves standard organic reactions, including acylation and alkylation methods. Understanding these processes is essential for chemists interested in synthetic pathways.
  • Laboratory Applications: In addition to its pharmaceutical use, this compound may serve as an intermediate in various chemical syntheses, highlighting the versatility of its functional groups.

Scientists and students alike are continually fascinated by how compounds like 2-(dimethylamino)ethyl 2-(4-chlorophenoxy)acetate; hydrochloride not only demonstrate the beauty of organic chemistry but also hold the potential for improving healthcare outcomes.

Synonyms
Meclofenoxate hydrochloride
Meclofenoxate HCl
Centrophenoxine hydrochloride
Lucidril
Helfergin
Marucotol
Brenal
Cellative
Proserout
Acefen
Centrophenoxine
Centrofenoxin
Methoxynal
Amipolen
Lutiaron
Meclophenoxate hydrochloride
235 Anp hydrochloride
Centrophenoxine (VAN)
Dimethylaminoethyl p-chlorophenoxyacetate hydrochloride
Meclofenoxate hydrochloride [JAN]
NSC 4268
Chlorowodorki centrofenoksyna
EINECS 222-975-3
UNII-5BK3070BDY
Centrophenoxine HCl
Chlorowodorki centrofenoksyna [Polish]
Lucidril (TN)
Clocete
NSC 113619
5BK3070BDY
DTXSID8045141
Dimethylaminoethyl 4-chlorophenoxyacetate hydrochloride
NSC-4268
NSC-113619
ACEPHEN HYDROCHLORIDE
DTXCID6025141
MECLOFENOXANE HYDROCHLORIDE
Dimethylaminoethyl ester of p-chlorophenoxyacetic acid hydrochloride
(p-Chlorophenoxy)acetic acid 2-(dimethylamino)ethyl ester hydrochloride
MECLOFENOXATE HYDROCHLORIDE [MI]
MECLOFENOXATE HYDROCHLORIDE [MART.]
MECLOFENOXATE HYDROCHLORIDE [WHO-DD]
ACETIC ACID, (p-CHLOROPHENOXY)-, 2-DIMETHYLAMINOETHYL ESTER, HYDROCHLORIDE
Acetic acid, 2-(4-chlorophenoxy)-, 2-(dimethylamino)ethyl ester, hydrochloride (1:1)
2-(DIMETHYLAMINO)ETHYL(P-CHLORPHENOXY)ACETATE HYDROCHLORIDE
(4-CHLOROPHENOXY)ACETIC ACID 2-(DIMETHYLAMINO)ETHYL ESTER HYDROCHLORIDE
MECLOFENOXATE HYDROCHLORIDE (MART.)
Meclofenoxate hydrochloride (JP17)
2-(Dimethylamino)ethyl (4-chlorophenoxy)acetate monohydrochloride
222-975-3
3685-84-5
Cerutil
Atsefen
Meclofenoxate (hydrochloride)
2-(dimethylamino)ethyl 2-(4-chlorophenoxy)acetate hydrochloride
2-(Dimethylamino)ethyl (p-chlorophenoxy)acetate hydrochloride
Lucidryl hydrochloride
Meclofenoxate (Centrophenoxine) HCl
WLN: GR DO1VO2N1&1 &GH
2-(dimethylamino)ethyl (4-chlorophenoxy)acetate hydrochloride
SR-01000075788
NCGC00015279-02
CAS-3685-84-5
Acetic acid, 2-(dimethylamino)ethyl ester hydrochloride
(Dimethylamino)ethyl ester of (p-chlorophenoxy)acetic acid hydrochloride
Prestwick_978
MFCD00012533
4-chlorophenoxy-acetic acid 2-(dimethylamino)ethyl ester hydrochloride
MLS002153989
SCHEMBL218322
SPECTRUM1503226
CHEMBL1256131
NSC4268
FIVHOHCAXWQPGC-UHFFFAOYSA-N
GLXC-04496
HMS1570I08
HMS1922K09
Pharmakon1600-01503226
Centrophenoxine hydrochloride, 99%
2-(dimethylamino)ethyl 2-(4-chlorophenoxy)acetate;hydrochloride
BCP21567
Meclofenoxate hydrochloride (JP18)
Tox21_110123
Tox21_302398
Tox21_500250
CCG-39961
HY-17555R
NSC113619
NSC758420
s4280
2-(4-Chlorophenoxy)acetic Acid 2-(Dimethylamino)ethyl Ester Hydrochloride
AKOS008968424
Tox21_110123_1
AC-1680
FM25029
KS-1179
LP00250
NSC-758420
Meclofenoxate (hydrochloride) (Standard)
NCGC00015279-08
NCGC00093712-01
NCGC00093712-02
NCGC00093712-03
NCGC00093712-04
NCGC00180932-01
NCGC00256151-01
NCGC00260935-01
HY-17555
SMR001233323
DB-049021
EU-0100250
M2460
NS00082919
SW197063-3
EN300-35717
C 8773
D02243
H10771
SR-01000075788-1
SR-01000075788-5
SR-01000075788-6
Q27261792
Z57281900
Meclofenoxate Hydrochloride 1.0 mg/ml in Acetonitrile (as free base)
2-(4-Chlorophenoxy)acetic acid 2-(dimethylamino)ethyl ester hydrochloride;2-(Dimethylamino)ethyl (p-chlorophenoxy)acetate hydrochlor ide;Acefen