D0632

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D0632

Sigma-Aldrich

 

DL-Dithiothreitol

≥98% (TLC), ≥99% (titration)

Synonym:threo-1,4-Dimercapto-2,3-butanediol, Cleland’s reagent, DTT
CAS Number:3483-12-3
Linear Formula:HSCH2CH(OH)CH(OH)CH2SH
Molecular Weight:154.25
Beilstein Registry Number:1719757
EC Number:222-468-7
MDL number:MFCD00004877
PubChem Substance ID:24893251

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Description

ApplicationAn excellent reagent for maintaining SH groups in reduced state; quantitatively reduces disulfides. DTT is effective in sample buffers for reducing protein disulfide bonds prior to SDS-PAGE. DTT can also be used for reducing the disulfide bridge of the cross-linker N,N′-bis(acryloyl)cystamine to break apart the matrix of a polyacrylamide gel. DTT is less pungent and is less toxic than 2-mercaptoethanol. Typically, a seven fold lower concentration of DTT (100 mM) is needed than is used for 2-mercaptoethanol (5% v/v, 700 mM).

Properties

assay≥98% (TLC)
 ≥99% (titration)
mp41-44 °C(lit.)
storage temp.2-8°C

Safety

Personal Protective EquipmentEyeshields, Faceshields, Gloves, Respirators
Hazard CodesXn
Risk Statements22-36/37/38
Safety Statements26-36
WGK Germany3
RTECSEK1610000
Flash Point(F)235.4 °F
Flash Point(C)113 °C

References

ReferenceCleland, W.W. Biochemistry 3, 480, (1964) Abstract
 Ruegg, U.T., Cleavage of disulfide bonds in proteins. Meth. Enzymol. 47, 111, (1977)
 Sears, D.W., In the investigation of incremental and kinetic reduction in proteins. Biochemistry 16, 2031, (1977)
 MacDonald, R.J., Isolation of RNA using guanidinium salts. Inclusion of a reductant enhances denaturation by breaking intramolecular protein disulfide bonds. Meth. Enzymol. 152, 219, (1987)
 Bacarese-Hamilton, A., Prevents the oxidation of cholecystokinin during its extraction from brain and duodenal tissues. Ann. N.Y. Acad. Sci. 448, 571, (1985)
 Jabusch, J.R., In protein sequence analysis. Anal. Biochem. 91, 532, (1978)
MerckMerck 13,3412
BeilsteinBeil. 1,III,2360
referenceAldrich MSDS 1, 840:C / Corp MSDS 1 (1), 1483:A / FT-IR 1 (1), 263:C / FT-IR 2 (1), 417:D / FT-NMR 1 (1), 424:A / IR-Spectra (3), 155:E / IR-Spectra (2), 139:A / NMR-Reference 2 (1), 230:B / RegBook 1 (1), 283:C / Sigma FT-IR 1 (2), 534:A / Structure Index 1, 38:E:8