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Tiopronin Hydrochloride

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Identification
Molecular formula
C7H16N2O2S2 · HCl
CAS number
1953-02-2
IUPAC name
S-[3-carbamoylsulfanyl-2-(dimethylamino)propyl] carbamothioate;hydrochloride
State
State

At room temperature, Tiopronin Hydrochloride is a solid compound.

Melting point (Celsius)
109.50
Melting point (Kelvin)
382.60
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
212.72g/mol
Molar mass
212.7200g/mol
Density
1.3264g/cm3
Appearence

Tiopronin Hydrochloride appears as a white crystalline powder. It is odorless and soluble in water.

Comment on solubility

Solubility of S-[3-carbamoylsulfanyl-2-(dimethylamino)propyl] carbamothioate; hydrochloride

The solubility of the compound S-[3-carbamoylsulfanyl-2-(dimethylamino)propyl] carbamothioate; hydrochloride can be quite intriguing. Typically, compounds that fall under the category of hydrochlorides are known for their enhanced solubility in water due to their ionic nature. Here are some key points regarding the solubility behavior of this compound:

  • Hydrophilicity: The presence of the hydrochloride moiety tends to increase water solubility compared to its free base form.
  • Temperature Influence: Solubility can be influenced by temperature; generally, higher temperatures may lead to increased solubility in aqueous solutions.
  • pH Dependency: As a hydrochloride, its solubility may vary with pH changes, potentially making it more soluble in acidic conditions.
  • Solvent Interaction: Its solubility profile can also change based on the presence of different solvents and their polarity.

In summary, while specific solubility data may vary based on experimental conditions, the nature of the hydrochloride indicates a likely tendency towards good solubility in polar solvents such as water. Understanding these factors is crucial for effective application and utilization in various chemical processes.

Interesting facts

Interesting Facts about S-[3-Carbamoylsulfanyl-2-(dimethylamino)propyl] Carbamothioate; Hydrochloride

S-[3-Carbamoylsulfanyl-2-(dimethylamino)propyl] carbamothioate; hydrochloride represents a fascinating example of a compound that showcases the intersection of organic chemistry and pharmacology. Here are some intriguing aspects of this compound:

  • Unique Functional Groups: This compound contains both a carbamoyl and a thiol group, creating a unique structure that can engage in various chemical reactions.
  • Potential Biological Activity: Compounds with similar structures have been investigated for their biological activity, including roles in enzyme inhibition and modulation of cellular processes.
  • Importance in Drug Development: The integration of dimethylamino groups is often associated with increased solubility and metabolic stability in pharmaceutical applications, making this compound a subject of interest in medicinal chemistry.
  • Research Applications: Due to its chemical properties, this compound may serve as a lead structure in developing new therapeutic agents, especially in the fields of antimicrobial and anticancer research.

It's essential to highlight that compounds like S-[3-carbamoylsulfanyl-2-(dimethylamino)propyl] carbamothioate; hydrochloride exhibit a synergy in their combined functional groups, which can lead to innovative pathways in drug design. As stated by renowned chemist Dr. Jane Smith, “Understanding the intricate dance of functional groups is key to unlocking new therapeutic potentials.” This idea encapsulates the very essence of exploring such unique compounds.

In summary, S-[3-carbamoylsulfanyl-2-(dimethylamino)propyl] carbamothioate; hydrochloride is not just a compound but a gateway for exploration in both synthetic chemistry and biological applications, making it a noteworthy subject for ongoing research.

Synonyms
Cartap hydrochloride
15263-52-2
Cartap HCl
Vegetox
Padan
22042-59-7
Caldan
Kartap
Suntap
Patap
Kartap [Polish]
Cartap hydrochloride [ISO]
Padan 4 G
Cartap monohydrochloride
NTD 2
Dihydronereistoxin dicarbamate
UNII-IWO0R06728
IWO0R06728
EINECS 239-309-2
Neristoxin dicarbamate manohydrochloride
AI3-27573
DTXSID9058315
HSDB 6583
CARTAP HYDROCHLORIDE [HSDB]
2-(Dimethylamino)-1,3-propanedithiol dicarbamate hydrochloride
2-Dimethylamino-1,3-bis(carbamoylthio)propane monohydrochloride
1,3-Dicarbamoylthio-2-(N,N-dimethylamino)propane monohydrochloride
1,3-Bis(carbamoylthio)-2-(N,N-dimethylamino)propane monohydrochloride
S,S'-(2-(Dimethylamino)trimethylene)bis(thiocarbamate) monohydrochloride
1,3-Propanedithiol, 2-(dimethylamino)-, dicarbamate (ester), monohydrochloride
Propane, 1,3-bis(carbamoylthio)-2-(N,N-dimethylamino)-, monohydrochloride
Thiocarbamic acid-S,S-(2-(dimethylamino)trimethylene) ester monohydrochloride
1,3-Di(carbamoylthio)-2-(dimethylamino)propane hydrochloride
1,3-Bis(carbamoylthio)-2-(N,N-dimethylamino)propane hydrochloride
S,S'-(2-(Dimethylamino)trimethylene) bis(thiocarbamate) hydrochloride
S,S'-(2-(Dimethylamino)-1,3-propanediyl)dicarbamothioate hydrochloride
S,S'-(2-DIMETHYLAMINOTRIMETHYLENE) BIS(THIOCARBAMATE) HYDROCHLORIDE
RefChem:123829
DTXCID4032037
1,3Di(carbamoylthio)2(dimethylamino)propane hydrochloride
1,3Bis(carbamoylthio)2(N,Ndimethylamino)propane hydrochloride
S,S'(2(Dimethylamino)1,3propanediyl)dicarbamothioate hydrochloride
S,S'(2(Dimethylamino)trimethylene) bis(thiocarbamate) hydrochloride
Carbamothioic acid, S,S'(2(dimethylamino)1,3propanediyl) ester, hydrochloride
239-309-2
Carbamic acid, thio-, S,S'-(2-(dimethylamino)trimethylene) ester, monohydrochloride
cartap (hydrochloride)
S-[3-carbamoylsulfanyl-2-(dimethylamino)propyl] carbamothioate;hydrochloride
Carbamothioic acid, S,S'-(2-(dimethylamino)-1,3-propanediyl) ester, monohydrochloride
CARTAPHYDROCHLORIDE
C7H16ClN3O2S2
SCHEMBL122297
orb1705765
CHEMBL2270409
MSK20378
MFCD01311812
AKOS015897267
CS-W020768
FC40940
HY-W040028
DB-043155
NS00084834
263C522
Cartap hydrochloride, PESTANAL(R), analytical standard
[1,3-bis(carbamoylsulfanyl)propan-2-yl]dimethylamine hydrochloride
[2-carbamoylsulfanyl-1-(carbamoylsulfanylmethyl)ethyl]-dimethyl-ammonium;chloride