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ChemicalBook--->CAS DataBase List--->156-57-0

156-57-0

156-57-0 Structure

156-57-0 Structure
IdentificationMore
[Name]

Cysteamine hydrochloride
[CAS]

156-57-0
[Synonyms]

2-AMINOETHANE-1-THIOL HYDROCHLORIDE
2-AMINOETHANETHIOL HCL
2-AMINOETHANETHIOL HYDROCHLORIDE
2-AMINOETHANOTHIOL HYDROCHLORIDE
2-AMINOETHYL MERCAPTAN HYDROCHLORIDE
2-MERCAPTOETHYLAMINE HCL
2-MERCAPTOETHYLAMINE HYDROCHLORIDE
BETA-MERCAPTOETHYLAMINE HYDROCHLORIDE
B-MERCAPTOETHYLAMINE HYDROCHLORIDE
CYSTEAMINE HCL
CYSTEAMINE HYDROCHLORIDE
CYSTEAMINIUM CHLORIDE
DECARBOXYCYSTEINE HCL
DECARBOXYCYSTEINE HYDROCHLORIDE
Mercaptamine hydrochloride
mercaptoethylammonium chloride
THIOETHANOLAMINE HYDROCHLORIDE
2-amino-ethanethiohydrochloride
2-Aminoethylmercaptarhydrochloride
2-mercapto-ethylaminhydrochloride
[EINECS(EC#)]

205-858-1
[Molecular Formula]

C2H8ClNS
[MDL Number]

MFCD00012904
[Molecular Weight]

113.61
[MOL File]

156-57-0.mol
Chemical PropertiesBack Directory
[Appearance]

White Solid
[Melting point ]

67-71 °C
[Boiling point ]

238.5℃[at 101 325 Pa]
[density ]

0.75
[vapor pressure ]

5.333Pa at 25℃
[refractive index ]

1.6100 (estimate)
[storage temp. ]

2-8°C
[solubility ]

H2O: 1 m at 20 °C, clear, colorless
[form ]

Crystalline Powder or Pellets
[color ]

White
[PH]

3.3-5.0 (400g/l, H2O, 20℃)
[Stability:]

Stable, but hygroscopic. Incompatible with strong oxidizing agents.
[biological source]

synthetic (organic)
[Water Solubility ]

VERY SOLUBLE
[Sensitive ]

Hygroscopic
[Usage]

Used as an antioxidant and in radiation therapy
[λmax]

λ: 280 nm Amax: ≤0.3
[Merck ]

14,2779
[BRN ]

3590083
[InChIKey]

OGMADIBCHLQMIP-UHFFFAOYSA-N
[LogP]

-2.14 at 25℃
[CAS DataBase Reference]

156-57-0(CAS DataBase Reference)
[EPA Substance Registry System]

156-57-0(EPA Substance)
[Absorption]

cut-off at 270nm in H2O at 1M
Safety DataBack Directory
[Hazard Codes ]

Xn,Xi
[Risk Statements ]

R22:Harmful if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[RIDADR ]

UN 3335
[WGK Germany ]

3
[RTECS ]

KJ0200000
[F ]

1-3-10-13
[TSCA ]

Yes
[HS Code ]

29309070
[Toxicity]

LD50 orally in Rabbit: 642 mg/kg
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Hydrochloric acid-->Sulfuric acid-->Carbon disulfide-->Monoethanolamine
[Preparation Products]

1,3-THIAZOLIDIN-2-ONE-->2-AMINOETHYLMETHYLSULFONE HYDROCHLORIDE-->THIAZOLIDINE-->Cystamine dihydrochloride-->N-(2-MERCAPTOETHYL)ACETAMIDE-->Thiazolidine, hydrochloride (1:1)-->2-METHYLTHIAZOLIDINE-->3-Thiomorpholineacetic acid, methyl ester-->2-(butylthio)ethanamine-->2-(3-Methylphenyl)thiazolidine, 97%-->S-BENZOYLCYSTEAMINE HYDROCHLORIDE-->2-(propylthio)ethanamine(SALTDATA: HCl)
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

Cysteamine hydrochloride(156-57-0).msds
Hazard InformationBack Directory
[Hazard]

Toxic by inhalation and ingestion.
[Description]

Cysteamine is a stable aminothiol with radioprotective activities. It reduces ionizing radiation-induced death and chromosomal damage in mice in a dose-dependent manner. Cysteamine binds rapidly and temporarily to plasma proteins upon administration and this activity is directly correlated to its radioprotective effects. In vitro, 0.1 mM cysteamine depletes 90% of free cystine from cystinotic fibroblasts. Formulations containing cysteamine have been used to treat nephropathic cystinosis and reduce glomerular deterioration in humans.
[Chemical Properties]

White Solid
[Uses]

Cysteamine hydrochloride is used as an antioxidant and in radiation therapy.
[General Description]

Cysteamine is an aminothiol that can reduce important oxidized disulfide molecules such as cystine to yield cysteine.
[Biochem/physiol Actions]

Cysteamine is an aminothiol that can reduce important oxidized disulfide molecules such as cystine to yield cysteine. Cysteamine is used in a wide range of applications from regulation of gene expression, to depletion of somatostatin, to coating of nanoparticles.
[Synthesis]

In particular to synthesizing cysteamine hydrochloride in alkali surroundings, which is characterized in that ethanolamine solution and sulfate solution are used as raw material; 2- amino ethyl sulfate is firstly synthesized before made into ring in alkaline solution by 2-amino ethyl sulfate and carbon disulfide, thereby getting Alpha -mercaptothiazoline; alkaline hydrolysis is made upon Alpha -mercaptothiazoline to produce cysteamine hydrochloride.
[Purification Methods]

Purify the salt by recrystallisation from EtOH. It is freely soluble in H2O and should be stored in a dry atmosphere. [Mills & Bogert J Am Chem Soc 62 1177 1940.] The picrate has m 125-126o; see previous entry for free base. [Beilstein 4 IV 1570.]
Spectrum DetailBack Directory
[Spectrum Detail]

Cysteamine hydrochloride(156-57-0)1HNMR
Cysteamine hydrochloride(156-57-0)13CNMR
Cysteamine hydrochloride(156-57-0)IR1
Cysteamine hydrochloride(156-57-0)IR2
Cysteamine hydrochloride(156-57-0)IR3
Cysteamine hydrochloride(156-57-0)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

2-Aminoethanethiol hydrochloride, 98%(156-57-0)
[Alfa Aesar]

2-Mercaptoethylamine hydrochloride, 98+%(156-57-0)
[Sigma Aldrich]

156-57-0(sigmaaldrich)
[TCI AMERICA]

2-Aminoethanethiol Hydrochloride,>95.0%(T)(156-57-0)
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