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2-({2-[bis(carboxymethyl)amino]ethyl}(carboxymethyl)amino)acetic acid; 2-amino-2-(hydroxymethyl)propane-1,3-diol; boric acid
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ChemBase ID:
153117
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Molecular Formular:
C14H30BN3O14
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Molecular Mass:
475.2107
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Monoisotopic Mass:
475.18208306
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SMILES and InChIs
SMILES:
B(O)(O)O.C(CN(CC(=O)O)CC(=O)O)N(CC(=O)O)CC(=O)O.C(C(CO)(CO)N)O
Canonical SMILES:
OC(=O)CN(CC(=O)O)CCN(CC(=O)O)CC(=O)O.OB(O)O.OCC(CO)(CO)N
InChI:
InChI=1S/C10H16N2O8.C4H11NO3.BH3O3/c13-7(14)3-11(4-8(15)16)1-2-12(5-9(17)18)6-10(19)20;5-4(1-6,2-7)3-8;2-1(3)4/h1-6H2,(H,13,14)(H,15,16)(H,17,18)(H,19,20);6-8H,1-3,5H2;2-4H
InChIKey:
OSBLTNPMIGYQGY-UHFFFAOYSA-N
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Cite this record
CBID:153117 http://www.chembase.cn/molecule-153117.html
NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
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2-({2-[bis(carboxymethyl)amino]ethyl}(carboxymethyl)amino)acetic acid; 2-amino-2-(hydroxymethyl)propane-1,3-diol; boric acid
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IUPAC Traditional name
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boric acid; edta; tris buffer
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Synonyms
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TBE buffer
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Tris-Borate-EDTA buffer
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TBE 缓冲液
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Tris-硼酸-EDTA 缓冲液
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MDL Number
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PubChem SID
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PubChem CID
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DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
CALCULATED PROPERTIES
CALCULATED PROPERTIES
JChem
Acid pKa
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1.486185
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H Acceptors
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10
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H Donor
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4
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LogD (pH = 5.5)
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-10.586659
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LogD (pH = 7.4)
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-14.721412
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Log P
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-5.221795
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Molar Refractivity
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62.3456 cm3
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Polarizability
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24.69443 Å3
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Polar Surface Area
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155.68 Å2
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Rotatable Bonds
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14
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Lipinski's Rule of Five
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true
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PROPERTIES
PROPERTIES
Physical Property
Safety Information
Product Information
Bioassay(PubChem)
Apperance
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powder blend
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Show
data source
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working solution
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Show
data source
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European Hazard Symbols
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Toxic (T)
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Show
data source
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MSDS Link
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German water hazard class
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1
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Show
data source
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2
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Show
data source
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Risk Statements
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60-61
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Show
data source
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60-61-36/37/38
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Show
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Safety Statements
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23-24/25
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Show
data source
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53-26-45
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Show
data source
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53-45
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data source
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GHS Pictograms
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GHS Signal Word
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Danger
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Show
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GHS Hazard statements
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H315-H319-H335-H360
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data source
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H315-H319-H360
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Show
data source
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H360FD
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Show
data source
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GHS Precautionary statements
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P201-P261-P305 + P351 + P338-P308 + P313
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Show
data source
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P201-P305 + P351 + P338-P308 + P313
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Show
data source
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P201-P308 + P313
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Show
data source
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Personal Protective Equipment
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Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
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Show
data source
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Eyeshields, Gloves, type P2 (EN 143) respirator cartridges
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Show
data source
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Grade
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for molecular biology
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Show
data source
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Suitability
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suitable for electrophoresis
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Show
data source
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suitable for gel electrophoresis (after dilution to working concentration)
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Show
data source
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Impurities
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≤5 ppm heavy metals (as Pb)
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Show
data source
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bioburden, tested
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Show
data source
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DNase and RNase, none detected
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Show
data source
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DNase, RNase and NICKase, none detected
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Show
data source
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DNase, RNase, Protease, none detected
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Show
data source
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Dnase, RNase, Protease, tested
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Show
data source
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endotoxin, tested
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Show
data source
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Sterility
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0.2 μm filtered
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Show
data source
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sterile; 0.2 μm filtered
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Show
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Quality Level
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ELITE
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Show
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GMP
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Product Line
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BioReagent
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data source
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DETAILS
DETAILS
Sigma Aldrich
Sigma Aldrich -
T9525
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Application TBE running buffer is the most commonly used buffer for DNA and RNA polyacrylamide gel electrophoresis.1, TBE is used with non-denaturing or denaturing (7 M urea) gels. It is also routinely used for DNA automated sequencing gel.2 TBE can also be used for agarose gels but is not recommended for preparative gels for recovery of nucleic acids. Dilution of the TBE stock concentrates to a 1× TBE running buffer results in a buffer containing 89 mM Tris-borate and 2 mM EDTA, pH 8.3. The 5× or 10× stocks may also be added to an acrylamide/bis-acrylamide stock solution for making the PAGE gel. Applied voltages of less than 5 V/cm (distance between the electrodes of the unit) are recommended for maximum resolution. Other Notes 89 mM Tris borate, pH approx. 8.3, containing 2 mM EDTA. Packaging Supplied in dispenser with a spigot. Preparation Note Prepared with Biotechnology Performance Certified Trizma base (Product Code T6066) and Molecular Biology Reagents boric acid (Product Code B6768) and EDTA disodium salt (Product Code E5134). Solution prepared with 18 megohm water |
Sigma Aldrich -
T4415
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Application Ready for use in gel electrophoresis after dilution to working concentrations. TBE running buffer is the most commonly used buffer for DNA and RNA polyacrylamide gel electrophoresis. TBE is used with non-denaturing or denaturing (7 M urea) gels. It is also routinely used for DNA automated sequencing gel. TBE can also be used for agarose gels but is not recommended for preparative gels for recovery of nucleic acids. Dilution of the TBE stock concentrates to a 1× TBE running buffer results in a buffer containing 89 mM Tris-borate and 2 mM EDTA, pH 8.3. The 5× or 10× stocks may also be added to an acrylamide/bis-acrylamide stock solution for making the PAGE gel. Applied voltages of less than 5 V/cm (distance between the electrodes of the unit) are recommended for maximum resolution. Other Notes TBE buffer is prone to precipitation over time. Precipitation generally will not adversely affect performance. Packaging The 4L, 10L and 20L sizes are supplied in dispenser with a spigot. Preparation Note Prepared with 18 megohm water Prepared with Biotechnology Performance Certified Trizma base (Product Code T6066) and Molecular Biology Reagents boric acid (Product Code B6768) and EDTA disodium salt (Product Code E5134). |
Sigma Aldrich -
T6400
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Application Ready for use in gel electrophoresis after dilution to working concentrations. TBE running buffer is the most commonly used buffer for DNA and RNA polyacrylamide gel electrophoresis. TBE is used with non-denaturing or denaturing (7 M urea) gels. It is also routinely used for DNA automated sequencing gel. TBE can also be used for agarose gels but is not recommended for preparative gels for recovery of nucleic acids. Dilution of the TBE stock concentrates to a 1× TBE running buffer results in a buffer containing 89 mM Tris-borate and 2 mM EDTA, pH 8.3. The 5× or 10× stocks may also be added to an acrylamide/bis-acrylamide stock solution for making the PAGE gel. Applied voltages of less than 5 V/cm (distance between the electrodes of the unit) are recommended for maximum resolution. Other Notes 0.445 M Tris borate, pH approx. 8.3, containing 0.01 M EDTA. Packaging Supplied in dispenser with a spigot. Preparation Note Prepared with Biotechnology Performance Certified Trizma base (Product Code T6066) and Molecular Biology Reagents boric acid (Product Code B6768) and EDTA disodium salt (Product Code E5134). Solution prepared with 18 megohm water |
Sigma Aldrich -
T4448
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Application TBE running buffer is the most commonly used buffer for DNA and RNA polyacrylamide gel electrophoresis.1, TBE is used with non-denaturing or denaturing (7 M urea) gels. It is also routinely used for DNA automated sequencing gel.2 TBE can also be used for agarose gels but is not recommended for preparative gels for recovery of nucleic acids. Dilution of the TBE stock concentrates to a 1× TBE running buffer results in a buffer containing 89 mM Tris-borate and 2 mM EDTA, pH 8.3. The 5× or 10× stocks may also be added to an acrylamide/bis-acrylamide stock solution for making the PAGE gel. Applied voltages of less than 5 V/cm (distance between the electrodes of the unit) are recommended for maximum resolution. General description Made with WFI water; contains 0.445 M Tris-borate, 10 mM EDTA, at pH ~8.3. Packaging Supplied in a dispenser with a spigot Preparation Note Prepared with Biotechnology Performance Certified Trizma base (Product Code T6066) and Molecular Biology Reagents boric acid (Product Code B6768) and EDTA disodium salt (Product Code E5134). |
Sigma Aldrich -
T7527
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Application Ready for use in gel electrophoresis after dilution to working concentrations. TBE running buffer is the most commonly used buffer for DNA and RNA polyacrylamide gel electrophoresis. TBE is used with non-denaturing or denaturing (7 M urea) gels. It is also routinely used for DNA automated sequencing gel. TBE can also be used for agarose gels but is not recommended for preparative gels for recovery of nucleic acids. Dilution of the TBE stock concentrates to a 1× TBE running buffer results in a buffer containing 89 mM Tris-borate and 2 mM EDTA, pH 8.3. The 5× or 10× stocks may also be added to an acrylamide/bis-acrylamide stock solution for making the PAGE gel. Applied voltages of less than 5 V/cm (distance between the electrodes of the unit) are recommended for maximum resolution. Packaging The 1-liter size is packaged in a plastic bottle large enough to contain the 5× concentrate. Preparation Note Prepared with Biotechnology Performance Certified Trizma base (Product Code T6066) and Molecular Biology Reagents boric acid (Product Code B6768) and EDTA disodium salt (Product Code E5134). Reconstitution Produces a 5× concentrate (0.445 M Tris-borate, 10 mM EDTA, pH 8.3) after dissolving with the indicated amount of water. |
Sigma Aldrich -
T3913
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Application TBE running buffer is the most commonly used buffer for DNA and RNA polyacrylamide gel electrophoresis.1, TBE is used with non-denaturing or denaturing (7 M urea) gels. It is also routinely used for DNA automated sequencing gel.2 TBE can also be used for agarose gels but is not recommended for preparative gels for recovery of nucleic acids. Dilution of the TBE stock concentrates to a 1× TBE running buffer results in a buffer containing 89 mM Tris-borate and 2 mM EDTA, pH 8.3. The 5× or 10× stocks may also be added to an acrylamide/bis-acrylamide stock solution for making the PAGE gel. Applied voltages of less than 5 V/cm (distance between the electrodes of the unit) are recommended for maximum resolution. Packaging Packaged in pouches Preparation Note Prepared with Biotechnology Performance Certified Trizma base (Product Code T6066) and Molecular Biology Reagents boric acid (Product Code B6768) and EDTA disodium salt (Product Code E5134). Reconstitution Produces a 5× concentrate (0.445 M Tris-borate, 10 mM EDTA, pH 8.3) after dissolving with the indicated amount of water. A suitable container must be supplied. |
Sigma Aldrich -
T4323
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Application TBE running buffer is the most commonly used buffer for DNA and RNA polyacrylamide gel electrophoresis.1, TBE is used with non-denaturing or denaturing (7 M urea) gels. It is also routinely used for DNA automated sequencing gel.2 TBE can also be used for agarose gels but is not recommended for preparative gels for recovery of nucleic acids. Dilution of the TBE stock concentrates to a 1× TBE running buffer results in a buffer containing 89 mM Tris-borate and 2 mM EDTA, pH 8.3. The 5× or 10× stocks may also be added to an acrylamide/bis-acrylamide stock solution for making the PAGE gel. Applied voltages of less than 5 V/cm (distance between the electrodes of the unit) are recommended for maximum resolution. Caution TBE buffer is prone to precipitation over time. Precipitation generally will not adversely affect performance. Preparation Note Prepared with Biotechnology Performance Certified Trizma base (Product Code T6066) and Molecular Biology Reagents boric acid (Product Code B6768) and EDTA disodium salt (Product Code E5134). |
PATENTS
PATENTS
PubChem Patent
Google Patent