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4781-83-3

4781-83-3 Structure

4781-83-3 Structure
IdentificationMore
[Name]

2-IMINOTHIOLANE
[CAS]

4781-83-3
[Synonyms]

2-IMINOTHIOLANE
2-IMINOTHIOLANE HCL
2-IMINOTHIOLANE HYDROCHLORIDE
2-THIOLANIMINE HYDROCHLORIDE
DIHYDRO-2(3H)-THIOPHENIMINE HYDROCHLORIDE
METHYL 4-MERCAPTOBUTYRIMIDATE HYDROCHLORIDE
TRAUT'S REAGENT
Methyl-4-mercaptobutyrimidate hydrochloride 2-Iminothiolane hydrochloride
2(3H)-Thiophenimine, dihydro-, hydrochloride
2-Thiolanimine hydrochloride, 2IT, Dihydro-2(3H)-thiophenimine hydrochloride, Trauts reagent
2-Furancarboxyaldehyde, Reagent
[EINECS(EC#)]

800-330-2
[Molecular Formula]

C4H7NS
[MDL Number]

MFCD00216010
[Molecular Weight]

101.17
[MOL File]

4781-83-3.mol
Chemical PropertiesBack Directory
[Appearance]

White Crystalline Solid
[Melting point ]

198-201 °C(lit.)
[storage temp. ]

2-8°C
[solubility ]

H2O: 100 mg/mL
[form ]

powder
[color ]

White to Off-White
[Water Solubility ]

Freely soluble in water
[Usage]

A valuable tool in studies of cellular organelles and oligomeric enzymes, using the techniques of protein-protein cross-linking. It may also be used to introduce reactive sulfhydryl groups into proteins for subsequent reaction with alkylating agen
[BRN ]

3620079
[InChI]

InChI=1S/C4H7NS.ClH/c5-4-2-1-3-6-4;/h5H,1-3H2;1H
[InChIKey]

ATGUDZODTABURZ-UHFFFAOYSA-N
[SMILES]

C1(=N)SCCC1.Cl
[CAS DataBase Reference]

4781-83-3(CAS DataBase Reference)
Safety DataBack Directory
[Safety Statements ]

S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

3
[F ]

1-3-10
[HS Code ]

29349990
[Storage Class]

6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
[Hazard Classifications]

Acute Tox. 3 Oral
Hazard InformationBack Directory
[Chemical Properties]

White Crystalline Solid
[Uses]

2-Iminothiolane hydrochloride is a valuable tool in studies of cellular organelles and oligomeric enzymes, using the techniques of protein-protein cross-linking. It may also be used to introduce reactive sulfhydryl groups into proteins for subsequent reaction with alkylating agents or heavy metal compounds.
[Uses]

2-Iminothiolane hydrochloride is predominantly used as an amine reactive at pH 7-10 and is also an effective thiolation reagent for polysaccharides. It is also used as a RNA-protein crosslinking reagent as well as useful in cross-linking proteins..
[Uses]

Cross-linking reagent cleavable by thiols.
[General Description]

2-Iminothiolane hydrochloride (2-IT.HCl), a protein modification reagent, is commonly employed to attach thiol groups to proteins and peptides. Raman spectroscopic analysis of hair keratin fibers modified with 2-IT.HCl showed the formation of new disulfide groups.
[Purification Methods]

Recrystallise the hydrochloride from MeOH/Et2O (m 187-192o) or (MeOH/Me2CO), but after sublimation at ~180o/0.2mm the melting point rises to 202-203o. It has 1HNMR with 2.27 (2H, t), 3.25 (2H, t) and 3.52 (2H, t) in (CD3)2SO. [King et al. Biochemistry 17 1499 1978.] The free base is purifed by vacuum distillation (b 71-72o/6mm) with IR (film) with 1700 (C=N)cm-1 and 1HNMR (CDCl3) with at 3.58 (2H, t) and max 2.10-2.8 (4H, m). The free base is stable on storage but slowly hydrolyses in aqueous solutions with half-lives at 25o of 390hours at pH 9.1, 210hours at pH 10 and 18hours at pH 11. [Traut et al. Biochemistry 12 3266 1973, Biochemistry 17 399 1978, Alagon & King Biochemistry 19 4343 1980, Beilstein 17/9 V 12.]
Spectrum DetailBack Directory
[Spectrum Detail]

2-IMINOTHIOLANE(4781-83-3)1HNMR
2-IMINOTHIOLANE(4781-83-3)IR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

4781-83-3(sigmaaldrich)
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