DL-Dithiothreitol ...

DL-Dithiothreitol 3483-12-3

DL-Dithiothreitol 3483-12-3

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1 Kilogram

Negotiable

  • Min.Order :1 Kilogram
  • Purity: 99.0%
  • Payment Terms : L/C,D/A,D/P,T/T,Other

Keywords

DL-Dithiothreitol 3483-12-3 DL-Dithiothreitol

Quick Details

  • Appearance:White crystalline powder
  • Application: For Organic Synthesis use
  • PackAge:IN 25kg drums
  • ProductionCapacity:10|Metric Ton|Month
  • Storage:In Room Temperature
  • Transportation:As Per MSDS

Superiority:

Product Name: DL-1,4-Dithiothreitol
Synonyms: DL-THREO-2,3-DIHYDROXY-1,4-DITHIOLBUTANE;DL-2,3-DIHYDROXY-1,4-BUTANEDITHIOL;DL-1,4-DIMERCAPTO-2,3-BUTANEDIOL;DL-1,4-DITHIOTHREITOL;DITT;(+/-)-DITHIOTHREITOL;DITHIOTHREITOL;DITHIOTHREITOL, 1,4-
CAS: 3483-12-3
MF: C4H10O2S2
MW: 154.25
EINECS: 222-468-7
Product Categories: Chemistry;APIS;Cleland's Reagent;Protein Modification Reagents;Life Science Chemical Reagents;proteinmod
Mol File: 3483-12-3.mol
DL-1,4-Dithiothreitol Structure

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Details:

DL-1,4-Dithiothreitol Chemical Properties
mp  41-44 °C(lit.)
bp  125 °C
density  1.04 g/mL at 20 °C
Fp  >230 °F
storage temp.  2-8°C
solubility  H2O: 50 mg/mL, clear, colorless
Water Solubility  freely soluble
Sensitive  Air Sensitive
Merck  14,3376
BRN  1719757
Stability: Stability Stable, but heat sensitive. Incompatible with strong oxidizing agents. Keep frozen at -20 to -10 C.
CAS DataBase Reference 3483-12-3(CAS DataBase Reference)
NIST Chemistry Reference 2,3-Butanediol, 1,4-dimercapto-, (r*,r*)-(3483-12-3)
EPA Substance Registry System 2,3-Butanediol, 1,4-dimercapto-, (2R,3R)-rel-(3483-12-3)
 
Safety Information
Hazard Codes  Xn
Risk Statements  25-36/37/38-22-20/21/22
Safety Statements  26-45-37/39-36
WGK Germany  3
RTECS  EK1610000
F  3-10-16-23
HS Code  29309099
 
 
DL-1,4-Dithiothreitol Usage And Synthesis
Chemical Properties White crystalline powder
Usage Dithiothreitol is a redox reagent commonly used as a reducing agent for thiolated DNA. Dithiothreitol is also used to reduce the disulfide bonds of proteins.
Biological Activity Reagent for maintaining SH groups in the reduced state.

 

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