| Identification | More | [Name]
THIAZOLIDINE | [CAS]
504-78-9 | [Synonyms]
TETRAHYDROTHIAZOLE
THIAZOLIDINE
1,3-Thiazolidine
1-Thia-3-azacyclopentane
THIAZOLIDINE
TETRAHYDROTHIAZOLE
Thiazolidine ,98% | [EINECS(EC#)]
208-002-5 | [Molecular Formula]
C3H7NS | [MDL Number]
MFCD00005211 | [Molecular Weight]
89.16 | [MOL File]
504-78-9.mol |
| Chemical Properties | Back Directory | [Appearance]
clear colorless liquid | [Boiling point ]
72-75 °C/25 mmHg (lit.) | [density ]
1.131 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.5508(lit.)
| [Fp ]
133 °F
| [storage temp. ]
under inert gas (nitrogen or Argon) at 2–8 °C | [solubility ]
Chloroform (Sparingly), Methanol (Slightly) | [form ]
Liquid | [pka]
8.84±0.20(Predicted) | [color ]
Clear colorless | [Detection Methods]
GC | [InChI]
1S/C3H7NS/c1-2-5-3-4-1/h4H,1-3H2 | [InChIKey]
OGYGFUAIIOPWQD-UHFFFAOYSA-N | [SMILES]
C1CSCN1 | [LogP]
-1.725 (est) | [CAS DataBase Reference]
504-78-9(CAS DataBase Reference) | [Storage Precautions]
Store under nitrogen |
| Safety Data | Back Directory | [Hazard Codes ]
C | [Risk Statements ]
R34:Causes burns. | [Safety Statements ]
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
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 . | [RIDADR ]
UN 1993 3/PG 3
| [WGK Germany ]
3
| [RTECS ]
XJ5123700
| [REACH Registrations]
Active | [HazardClass ]
3 | [PackingGroup ]
III | [HS Code ]
29341000 | [Storage Class]
3 - Flammable liquids | [Hazard Classifications]
Flam. Liq. 3 |
| Hazard Information | Back Directory | [Chemical Properties]
clear colorless liquid | [Chemical Properties]
Thiazolidines are a class of hetrocyclic organic compounds having a 5 membered saturated ring with a thio ether group at 1 position and an amine group in the 3 position. It is sulfur analogue of oxazolidine. Thiazolidines may be synthesized by a condensation reaction between a thiol and an aldehyde or ketone. It is a reversible reaction. Therefore many thiazolidines are labile towards hydrolysis in aqueous solution. Hydrolysis of the thiazolidine generates the thiol and an aldehyde from which it was synthesized. | [Uses]
Thiazolidine was used in the synthesis of homogeneous penicillamine disulphide cross-linked polypeptides. | [Definition]
ChEBI: 1,3-thiazolidine is a thiazolidine. |
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| Company Name: |
J & K SCIENTIFIC LTD.
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18210857532 18210857532 |
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https://www.jkchemical.com |
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Alfa Aesar
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400-6106006 |
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http://chemicals.thermofisher.cn |
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Energy Chemical
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400-0056266 |
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www.energy-chemical.com |
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China Langchem Inc.
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0086-21-58956006 |
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www.chemicalbook.com/ShowSupplierProductsList19141/0_EN.htm |
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Spectrum Chemical Manufacturing Corp.
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021-021-021-67601398-809-809-809 15221380277 |
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