1,4-Dithio-DL-threitol

Catalog Number Size Price Stock Quantity
B2699-296120 10 g $294 In stock
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Product Information

Molecular Formula:
C4H10O2S2
Molecular Weight:
154.25
Description
Reagent for the quantitative reduction of disulfide group. Prevents the oxidation of cholecystokinin during its extraction from brain and duodenal tissues. Cleavage of disulfide bonds in proteins.
Synonyms
DL-1,4-Dithiothreitol; DTT; Cleland's reagent; threo-1,4-Dimercapto-2,3-butanediol; Dithiothreitol; dl-Dithiothreitol; 1,4-Dithiothreitol; D-Dtt; 1,4-Dithio-dl-threitol; DL-Dithiothreitol; threo-1,4-Dimercapto-2,3-butanediol
IUPAC Name
(2S,3S)-1,4-bis(sulfanyl)butane-2,3-diol
Canonical SMILES
C(C(C(CS)O)O)S
InChI
InChI=1S/C4H10O2S2/c5-3(1-7)4(6)2-8/h3-8H,1-2H2/t3-,4-/m1/s1
InChI Key
VHJLVAABSRFDPM-QWWZWVQMSA-N
Boiling Point
125.0-130.0 °C at 2 mmHg
Melting Point
41-44 °C
Flash Point
>230 °F
Purity
≥ 99 % (Assay by titration)
Density
1.040 g/mL at 20 °C
Solubility
Soluble in Water (50 mg/mL, clear, colorless)
Appearance
White crystals or free flowing powder
Application
Used as a reagent in biochemistry to prevent oxidation of thiol groups and to reduce disulfides to dithiols; Has been used as a radioprotectant; Dithiothreitol (DTT) is the common name for a small-molecule redox reagent known as Cleland's reagent.
Storage
Store at 2-8 °C
Refractive Index
1.5200 (estimate)
Stability
May decompose on exposure to moist air or water. Stable under recommended storage conditions
LogP
log Kow = -0.48 (est)
Vapor Pressure
1.28X10-4 mm Hg at 25 °C (est)
Henry's Law Constant
2.9X10-10 atm-cu m/mol at 25 °C (est)
Decomposition
Hazardous decomposition products formed under fire conditions: carbon oxides, Sulfur oxides
Odor
Characteristic

Safety Information

Hazards
H302:
Harmful if swallowed.
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
Precautionary Statement
P264:
Wash thoroughly after handling.
P270:
Do not eat, drink or smoke when using this product.
P280:
Wear protective gloves/protective clothing/eye protection/face protection.
P301+P312+P330:
IF SWALLOWED:
Call a POISON CENTER or doctor/physician if you feel unwell.
Rinse mouth.
P337+P313:
If eye irritation persists:
Get medical advice/attention.
P501:
Dispose of contents/container in accordance with local/regional/national/international regulations.
Signal Word
Danger

Computed Properties

XLogP3
-0.4
Hydrogen Bond Donor Count
4
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
3
Exact Mass
154.01222190 g/mol
Monoisotopic Mass
154.01222190 g/mol
Topological Polar Surface Area
42.5Ų
Heavy Atom Count
8
Formal Charge
0
Complexity
52
Isotope Atom Count
0
Defined Atom Stereocenter Count
2
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114134587-A Preparation method of high-performance regenerated pure keratin fiber 2021-12-24
CN-113304708-A Preparation method of glycoprotein microreactor with boron affinity surface imprinting of mesoporous molecular sieve 2021-06-11
CN-113068683-A Cell preservation solution for liquid-based cell examination and preparation method thereof 2021-03-03
WO-2022053525-A1 Array, soaking solutions and method of selecting soaking conditions for small molecules in biological macromolecular crystals 2020-09-08
WO-2022053528-A1 Array, soaking solutions and method of selecting soaking conditions for small molecules in biological macromolecular crystals 2020-09-08
WO-2022044759-A1 Composition containing semiconductor nanoparticles, color filter, and image display device 2020-08-31
WO-2022044761-A1 Composition containing semiconductor nanoparticles, color filter, and image display device 2020-08-31
JP-2022024764-A Antioxidants and their manufacturing methods, pharmaceutical compositions and their manufacturing methods, foods, and cosmetics 2020-07-28
WO-2022020288-A1 Antibody-conjugated chemical inducers of degradation of brm and methods thereof 2020-07-21
WO-2022006231-A1 Dpagt1 inhibitors of capuramycin analogues and their antimigratory activities of solid tumors 2020-06-30

Literatures

PMID Publication Date Title Journal
34244458 2021-10-01 Recruitment of endoplasmic reticulum-targeted and cytosolic mRNAs into membrane-associated stress granules RNA (New York, N.Y.)
31339623 2019-10-01 Unfolded protein response regulates P53 expression in the pulmonary endothelium Journal of biochemical and molecular toxicology
28837777 2017-09-18 Arsenite Binds to the Zinc Finger Motif of TIP60 Histone Acetyltransferase and Induces Its Degradation via the 26S Proteasome Chemical research in toxicology
25446071 2015-01-02 Impact of cadmium, cobalt and nickel on sequence-specific DNA binding of p63 and p73 in vitro and in cells Biochemical and biophysical research communications
23933410 2013-10-25 In vitro glutathione peroxidase mimicry of ebselen is linked to its oxidation of critical thiols on key cerebral suphydryl proteins - A novel component of its GPx-mimic antioxidant mechanism emerging from its thiol-modulated toxicology and pharmacology Chemico-biological interactions
23618698 2013-08-01 Determination of the warfarin inhibition constant Ki for vitamin K 2,3-epoxide reductase complex subunit-1 (VKORC1) using an in vitro DTT-driven assay Biochimica et biophysica acta
23710884 2013-08-01 Evaluation of warfarin resistance using transcription activator-like effector nucleases-mediated vitamin K epoxide reductase knockout HEK293 cells Journal of thrombosis and haemostasis : JTH
23261715 2013-02-25 Modulation of activity and inhibitor sensitivity of rabbit aldose reductase-like protein (AKR1B19) by oxidized glutathione and SH-reagents Chemico-biological interactions
22867017 2013-02-01 Disulfide bond as a switch for copper-zinc superoxide dismutase activity in asthma Antioxidants & redox signaling
22884002 2013-01-15 Sensitive and antifouling impedimetric aptasensor for the determination of thrombin in undiluted serum sample Biosensors & bioelectronics
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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