In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
May 1st, 2008 | 8 | No |
Popular Name: Dithioerythritol Dithioerythritol
Find On: PubMed — Wikipedia — Google
CAS Numbers: 12/3/3483 12:00:00 AM , 16096-97-2 , 27565-41-9 , 302912-05-6 , 3483-12-3 , 3483/12/3 , 6892-68-8 , [3483-12-3] , [6892-68-8]
(+/-)-threo-1,4-Dimercapto-2,3-butanediol
1,4-dimercapto-2,3-butanediol; 1,4-dimercaptobutane-2,3-diol
6892-68-8; C00950; DTE; Dithioerythritol; erythro-1,4-Dimercapto-2,3-butanediol
6892-68-8; DTE; dithioerythritol; erythro-1, 4-dimercapto-2,3-butanediol
CHEBI:23854; CHEBI:4664; CHEBI:11174
CHEBI:42239; CHEBI:4662; CHEBI:14184; CHEBI:23851
DITHIOERYTHREITOL molecular biology grade; [6892-68-8]
Dithioerythreitol [6892-68-8]; (DTE)
DL-Dithiothreitol [for Electrophoresis]
DL-threo-1,4-Dimercapto-2,3-butanediol
DL-threo-2,3-Dihydroxy-1,4-dithiobutane
erythro-1,4-Dimercapto-2,3-butanediol
Type pH range | xlogP | Des A‑Pol Apolar desolvation (kcal/mol) | Des Pol Polar desolvation (kcal/mol) | H Don H-bond donors | H Acc H-bond acceptors | Chg Net charge | tPSA (Ų) | MWT Molecular weight (g/mol) | RB Rotatable bonds | DL |
---|---|---|---|---|---|---|---|---|---|---|
Ref Reference (pH 7) | -0.33 | -2.14 | -6.43 | 2 | 2 | 0 | 40 | 154.256 | 3 | ↓ |
Hi High (pH 8-9.5) | -0.33 | -1.28 | -96.44 | 2 | 2 | -2 | 40 | 152.24 | 3 | ↓ |
Hi High (pH 8-9.5) | -0.33 | -1.66 | -37.68 | 2 | 2 | -1 | 40 | 153.248 | 3 | ↓ |
Note Type | Comments | Provided By |
---|---|---|
Boiling_Point | 125-130?/12mm | Alfa-Aesar |
Boiling_Point | 125-130°/12mm | Alfa-Aesar |
BP | 130 / 2 | TCI |
UniProt Database Links | 3XYN2_VIBSX; 3XYN_ALCSP; ACCA_PEA; ACCD_PEA; ADPRH_MOUSE; ADPRH_RAT; AGLB_THENE; AGTA_DICDI; ALDO1_ARATH; ALDO2_ARATH; ALLB_ECOLI; APQ13_YEAST; APR1_ARATH; APR2_ARATH; APR3_ARATH; CATLL_FASHE; CBAD1_ARTSP; CBAD2_ARTSP; CHAC1_HUMAN; CUL1_HUMAN; CUL1_MOUSE | ChEBI |
Melting_Point | 40-43? | Alfa-Aesar |
Melting_Point | 40-43° | Alfa-Aesar |
mp | 42 - 44 | MolMall (formerly Molecular Diversity Preservation International) |
MP | 43 | TCI |
Mp [°C] | 82 - 86 | Acros Organics |
M.P | 82-84 °C | Indofine |
Melting_Point | 82-84? | Alfa-Aesar |
Melting_Point | 82-84° | Alfa-Aesar |
MP | 84 | TCI |
MP | > 81 °C | Fluorochem |
Purity | >99% | Fluorochem |
Patent Database Links | EP1531160; EP1547610; EP1710304; US2006035295; US2007190069; US2007212417; US2007269488; US2008220536; WO2007103528; WO2007128983; WO2007130373 | ChEBI |
Patent Database Links | EP1749533; EP1872792; US2004038934; US2004176570; US2005027009; US2006035295; US2006040943; US2006135759; US2007190069; US2008220536; WO2005110955; WO2007128983; WO2008151324 | ChEBI |
SOLUBILITY | H2O: 10 mg/mL, clear, colorless | Indofine |
H phrase | H302: Harmful if swallowed | Acros Organics |
H phrase | H302: Harmful if swallowed; H319: Causes serious eye irritation; H335: May cause respiratory irritation; H315: Causes skin irritation | Acros Organics |
UniProt Database Links | MCR_SULTO; NSMF_HUMAN; NSMF_RAT; UBGAT_SCUBA | ChEBI |
P phrase | P261: Avoid breathing dust/fume/gas/mist/vapors/spray | Acros Organics |
P phrase | P261: Avoid breathing dust/fume/gas/mist/vapors/spray; P301+ P312: IF SWALLOWED: Call a POISON CENTER or doctor/physician if you feel unwell; P302+ P352: IF ON SKIN: Wash with plenty of soap and water; P280: Wear protective gloves/protective clothing/eye | Acros Organics |
R phrase | R22: Harmful if swallowed. | Acros Organics |
R phrase | R22: Harmful if swallowed.; R36/37/38: Irritating to eyes, respiratory system and skin. | Acros Organics |
Notes | Reagent for maintaining -SH groups in reduced state | Apollo Scientific Bioactives |
S phrase | S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. | Acros Organics |
S phrase | S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.; S37/39: Wear suitable gloves and eye/face protection. | Acros Organics |
Patent Database Links | WO2007135242 | ChEBI |
Hazard | XN: Harmful | Acros Organics |
No pre-computed analogs available. Try a structural similarity search.