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DL-Dithiothreitol

CAS No.
3483-12-3
Chemical Name:
DL-Dithiothreitol
Synonyms
DTT;DITHIOTHREITOL;DL-1,4-DITHIOTHREITOL;1,4-DITHIOTHREITOL;1,4-DITHIO-DL-THREITOL;Sputolysin;Cleland's reagent;DTT-MBG;DITHIOTHRIETOL;cis-2,3-Dihydroxy-1,4-butanedithiol
CBNumber:
CB6342919
Molecular Formula:
C4H10O2S2
Molecular Weight:
154.25
MDL Number:
MFCD00004877
MOL File:
3483-12-3.mol
MSDS File:
SDS
Last updated:2024-11-19 23:02:33

DL-Dithiothreitol Properties

Melting point 41-44 °C(lit.)
Boiling point 125 °C
alpha -0.2~+0.2°(20℃/D)(c=5,H2O)
Density 1.04 g/mL at 20 °C
vapor density 5.3 (vs air)
vapor pressure 0.019-0.29Pa at 20-50℃
refractive index 1.5200 (estimate)
Flash point >230 °F
storage temp. -20°C (or 4°C short term).
solubility H2O: 50 mg/mL, clear, colorless
form Powder
pka pK1:8.9 (25°C)
color White
PH 4.0-6.0 (20-25℃, 0.1m in H2O)
Odor Unpleasant Odor
PH Range 4 - 6 at 15,4 g/l at 25 °C
Water Solubility freely soluble
λmax λ: 260 nm Amax: 0.400
λ: 280 nm Amax: 0.100
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.
InChIKey VHJLVAABSRFDPM-UHFFFAOYSA-N
LogP 0.07 at 25℃ and pH5
CAS DataBase Reference 3483-12-3(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII T8ID5YZU6Y
NIST Chemistry Reference 2,3-Butanediol, 1,4-dimercapto-, (r*,r*)-(3483-12-3)
EPA Substance Registry System 1,4-Dithiothreitol (3483-12-3)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS05,GHS07
Signal word  Danger
Hazard statements  H302-H315-H318
Precautionary statements  P264-P270-P280-P301+P312-P302+P352-P305+P351+P338
Hazard Codes  Xn
Risk Statements  25-36/37/38-22-20/21/22
Safety Statements  26-45-37/39-36
RIDADR  UN 3335
WGK Germany  3
RTECS  EK1610000
3-10-16-23
TSCA  Yes
HS Code  29309099
NFPA 704
1
2 1

DL-Dithiothreitol price More Price(112)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich DTT-RO DTT 1,4-Dithiothreitol 3483-12-3 2g $89.3 2024-03-01 Buy
Sigma-Aldrich DTT-RO DTT crystalline powder, =97% (Ellman′s reagent), Mr 154.3 3483-12-3 10G $251 2024-03-01 Buy
Sigma-Aldrich DTT-RO DTT 1,4-Dithiothreitol 3483-12-3 25g $547 2024-03-01 Buy
Sigma-Aldrich 646563 DL-Dithiothreitol solution 1?M in H2O 3483-12-3 10x0.5mL $107 2024-03-01 Buy
Sigma-Aldrich 233155 Cleland’s Reagent - CAS 3483-12-3 - Calbiochem 3483-12-3 5G $149 2024-03-01 Buy
Product number Packaging Price Buy
DTT-RO 2g $89.3 Buy
DTT-RO 10G $251 Buy
DTT-RO 25g $547 Buy
646563 10x0.5mL $107 Buy
233155 5G $149 Buy

DL-Dithiothreitol Chemical Properties,Uses,Production

Chemical Properties

Dithiothreitol (DTT), also known as Cleland's reagent, is a small-molecule redox reagent . Its oxidized form is a disulfide-bonded 6-membered ring. DTT has an epimeric ('sister') compound, dithioerythritol (DTE).
DTT is a white crystalline powder. It is highly soluble in water (clear solution, OD<0.05 at 0.02M), but also in ethanol, chloroform, ether and ethyl acetate.
DTT is an unusually strong reducing agent, with a redox potential of -0.33 V at pH 7. The pKa of thiol groups is typically ~8.3.
Dithiothreitol thiol-disulfide exchange reactions
The reduction of a typical disulfide bond proceeds by two sequential thiol-disulfide exchange reactions.

Uses

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.

Uses

DL-dithiothreitol (DTT) is a sulfhydryl compound that acts both as a reagent reducing disulfide bonds and as a protein denaturant on staphylococcal biofilm (Wu et al. 2011). Thanks to these properties, DTT is routinely used in clinical microbiology to liquefy respiratory specimens, but it has also been proven effective to detach biofilm from orthopaedic prosthesis (Drago et al. 2012, 2013). Since it is crucial to discriminate implant-related infections from aseptic loosening in orthopaedics, and because of the difficulty to diagnose subclinical infections, a prompt diagnosis of indwelling device-related infection is important for successful treatments (Borens et al. 2013). A fast microbiological diagnosis and bacterial identification should be recommended in order to set up a specific antimicrobial therapy. According to this strategy, the bacterial detachment from biofilm on explants should be accelerated by supporting the pathogen viability.

Definition

ChEBI: 1,4-dithiothreitol is the threo-diastereomer of 1,4-dimercaptobutane-2,3-diol. It has a role as a reducing agent, a chelator and a human metabolite. It is a dithiol and a 1,4-dimercaptobutane-2,3-diol.

Application

Dithiothreitol (DTT) is a water-soluble reducing reagent used for various applications in biotechnology, biology and biochemistry :
reduces quantitatively disulfides, generating sulfhydryls (used typically at 1-10mM for protein SS reduction)
reduction of proteins before SDS-PAGE analysis, studies of protein structure and function (Kaji 1993)
keep sulfhydryl groups of biomolecules in the reduced state - protects biomolecules in various applications (enzymes or receptors, living cells under ionizing radiations)
prevents the fading of fluorescence such as FITC labeled conjugates (Picciolo 1984)

General Description

1,4-Dithiothreitol (DTT) is the threo isomer of 2,3-dihydroxy-1,4-dithiolbutane, and an isomer of 1,4-dithioerythritol. DTT is used in molecular biology to maintain sulfhydryl (-SH) groups in the reduced state and for quantitative reduction of disulfide (-S-S-) groups, as described by Cleland in his pioneering publication from the 1960's. Its usefulness as an reducing agent stems from its water solubility and reduced odor compared to previous thiol compounds.
DTT is oxidized to the cyclic disulfide, and thereby ensures the reduction of other disulfides in solution. The disulfide reduction is complete in minutes at pH 8. DTT is less pungent and less toxic than 2-mercaptoethanol. Typically, a 7-fold lower concentration of DTT (100 mM) is required compared to 2-mercaptoethanol (5% v/v, 700 mM).

Biochem/physiol Actions

DL-Dithiothreitol denatures proteins by reducing the disulphide bonds and reducing them to SH groups. It also prevents intramolecular and intermolecular disulfide bond formation between cysteine residues of proteins.

Toxicology

The thiol-containing compound Dithiothreitol (DTT) is toxic to cultured cells by inducing the generation of reactive oxygen species that ultimately cause cell death. DTT treatment triggers the transcription of the canonical apoptosis regulators grim, hid, and rpr at low amounts. The amplitude of this induction declines with elevating DTT amounts. Through Live microscopy, Wang et al. have observed apoptotic cells, especially in the gut of DTT-treated flies. In parallel, low DTT amounts also activate the expression of the cuticle barrier component gene snsl. This indicates that a physical defense response is launched upon DTT contact. This combined measure is seemingly successful in preventing fly death. The expression of several known detoxification genes, including cyp6a2, cyp6a8, cyp12d1, and GstD2, is also enhanced through DTT contact[1].

References

[1] Yiwen Wang . “Toxicity of Dithiothreitol (DTT) to Drosophila melanogaster.” Toxicology Reports 8 (2021): Pages 124-130.

Synthesis

The most widely used DL-Dithiothreitol (DTT) synthetic method is to be raw material with Soviet Union's moss sugar alcohol, use potassium permanganate oxidation earlier, obtains the sulfo-intermediate again under the thioacetic acid effect, and this sulfo-intermediate of hydrolysis obtains DTT at last.
Yu discloses a synthesizing method of DL-Dithiothreitol.1,4-butylene glycol is used as an initiating raw material and undergoes an addition reaction with bromine at first to obtain 2,3-dibromo-1,4-butylene glycol; hydrolyzation under the catalyzation of alkali is carried out to obtain dioxirane; addition reaction with thioacetic acid is carried out to obtain dithiothreitol diacetate; and finally hydrolyzation under the catalyzation of alkali is carried out to obtain the DL-Dithiothreitol.

storage

Store lyophilized at 4°C, desiccated. In lyophilized form, the chemical is stable for 12 months. Once in solution, store at -20°C and use within 3 months to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.
DTT solutions should be prepared fresh daily. If improperly stored (including room temperature and solution forms) its reducing ability may be reduced. Exposure to air should be minimized, even though DTT has a lower tendency to be oxidized directly by air than other reducing agents.
Recorded half-life of DTT solutions at various pH and temperatures (all are in M potassium phosphate buffer):
pH 6.5 @ 20°C= 40 hours
pH 7.5 @ 20°C = 10 hours
pH 8.5 @ 20°C = 1.4 hours
pH 8.5 @ 0°C = 11 hours
pH 8.5 @ 40°C = 0.2 hours
pH 8.5 @20°C (+0.1 mM Cu2+) = 0.6 hours
pH 8.5 @20°C (+0.1 mM EDTA) = 4 hours

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View Lastest Price from DL-Dithiothreitol manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
DL-Dithiothreitol pictures 2024-11-22 DL-Dithiothreitol
3483-12-3
US $1.00 / g 1g 99% 200kg/month WUHAN FORTUNA CHEMICAL CO., LTD
DL-Dithiothreitol pictures 2024-11-22 DL-Dithiothreitol
3483-12-3
US $100.00-75.00 / kg 1kg 99% 5000Ton HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
DL-1,4-Dithiothreitol pictures 2024-11-22 DL-1,4-Dithiothreitol
3483-12-3
US $10.00 / kg 1kg 99% 20ton Hebei Zhuanglai Chemical Trading Co.,Ltd
  • DL-Dithiothreitol pictures
  • DL-Dithiothreitol
    3483-12-3
  • US $100.00-75.00 / kg
  • 99%
  • HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
DL-1,4-Dithiothreitol, 1M solution in water, for molecular biology Dithiothreitol ,98% DL-1,4-Dithiothreitol,DTT DTT DL-1,4-Dithiothreitol DL-Dithiothreitol ,99% [for Molecular biology] DL-1,4-Dithiothreitol, DNAse, RNAse and Protease free, for Molecular b DL-1,4-Dithiothreitol, DNAse, RNAse and Protease free, for Molecular biology, 99+% 1GR DL-1,4-Dithiothreitol, for biocheMistry, 99% 1GR DL-1,4-Dithiothreitol, for biocheMistry, 99% 5GR (+/-)-THREO-1,4-DIMERCAPTO-2,3-BUTANEDIOL THREO-1,4-DIMERCAPTO-2,3-BUTANEDIOL THREO-2,3-DIHYDROXY-1,4-DITHIOBUTANE THREO-2,3-DIHYDROXY-1,4-DITHIOLBUTANE DL-DITHIOTHREITOL SIGMAULTRA 1,4-DITHIO-DL-THREITOL SOL., FOR MOL. BI OL.,1 M IN WATER DL-DITHIOTHREITOL ELECTROPHORESIS*REAGEN T Dithiothreitol(D.T.T.) 1,4-Dithiothreitol=DTT Cleland's Reagent DL-2,3-Dihydroxy-1,4-butanedithiol DL-1,4-Dimercapto-2,3-butanediol DL-DTT Cleland's Reagent, Dithiothreitol, DTT DL-Dithiothreitol ,99% [for electrophoresis] DL-Dithiothreitol,threo-1,4-Dimercapto-2,3-butanediol, Cleland’s reagent, DTT (2S,3S)-1,4-diMercaptobutane-2,3-diol DL-Dithiothreitol (DTT) Solution,100MM DL-1,4-Dithiothreitol SynonyMs: Dithiothreitol Dithiothreitol, for Molecular biology DL-Dithiothreitol (DTT) Dithiothreitol, for electrophoresis 4-dimercapto-3-butanediod-threo-1 Cleland regent D-Dtt d-threo-1,4-dimercapto-2,3-butanediol D-threo-1,4-Dimercapto-2,3-butanediol, Threitol, 1,4-dithio- wr34678 DL-DITHIOTHREITOL DL-THREO-2,3-DIHYDROXY-1,4-DITHIOLBUTANE DL-2,3-DIHYDROXY-1,4-BUTANEDITHIOL DL-1,4-DIMERCAPTO-2,3-BUTANEDIOL DITT (+/-)-DITHIOTHREITOL DITHIOTHREITOL, 1,4- DL-DTT DTT (RACEMIC) CGMP DTT (2S,3S:2R,3R)-THREO-1,4-DIMERCAPTO-2,3-BUTANEDIOL 2,3-BUTANEDIOL, 1,4-DIMERCAPTO-(R*,R*)- RAC-CLELAND'S REAGENT SPUTOLYSIN(R) REAGENT (R,R)-1,4-DIMERCAPTO-2,3-BUTANEDIOL (R,R)-DITHIOTHREITOL 1,4-dithio-threito CLELAND'S REAGENT, IMMOBILIZED CLELAND'S REDUCTACRYL(TM) REAGENT CLELAND REAGENT RACEMIC 1,4-DITHIOTHREITHOL OXALIC ACID DIHYDRATE HIGH PURITY GRADE Dithiothritol