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Merck
CN

93361

TAPS

BioUltra, ≥99.5% (T)

Synonym(s):

N-[Tris(hydroxymethyl)methyl]-3-aminopropanesulfonic acid, [(2-Hydroxy-1,1-bis(hydroxymethyl)ethyl)amino]-1-propanesulfonic acid

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About This Item

Empirical Formula (Hill Notation):
C7H17NO6S
CAS Number:
Molecular Weight:
243.28
EC Number:
249-954-1
UNSPSC Code:
12161700
PubChem Substance ID:
Beilstein/REAXYS Number:
2452420
MDL number:
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product line

BioUltra

assay

≥99.5% (T)

impurities

insoluble matter, passes filter test

ign. residue

≤0.1% (as SO4)

pH

4.5-6.5 (25 °C, 0.1 M in H2O)

useful pH range

7.7-9.1

pKa 

8.4

mp

230-235 °C (dec.)

solubility

H2O: 0.1 M at 20 °C, clear, colorless

anion traces

chloride (Cl-): ≤50 mg/kg, sulfate (SO42-): ≤50 mg/kg

cation traces

Al: ≤5 mg/kg, As: ≤0.1 mg/kg, Ba: ≤5 mg/kg, Bi: ≤5 mg/kg, Ca: ≤10 mg/kg, Cd: ≤5 mg/kg, Co: ≤5 mg/kg, Cr: ≤5 mg/kg, Cu: ≤5 mg/kg, Fe: ≤5 mg/kg, K: ≤50 mg/kg, Li: ≤5 mg/kg, Mg: ≤5 mg/kg, Mn: ≤5 mg/kg, Mo: ≤5 mg/kg, Na: ≤50 mg/kg, Ni: ≤5 mg/kg, Pb: ≤5 mg/kg, Sr: ≤5 mg/kg, Zn: ≤5 mg/kg

λ

0.1 M in H2O

UV absorption

λ: 260 nm Amax: 0.012, λ: 280 nm Amax: 0.008

SMILES string

OCC(CO)(CO)NCCCS(O)(=O)=O

InChI

1S/C7H17NO6S/c9-4-7(5-10,6-11)8-2-1-3-15(12,13)14/h8-11H,1-6H2,(H,12,13,14)

InChI key

YNLCVAQJIKOXER-UHFFFAOYSA-N

Other Notes

For studies of electron transport and phosphorylation in chloroplast lamellae preparations; Affords good protection of oxyhaemoglobin from oxidation to methaemoglobin during freeze-drying; Background electrolyte in protein trace analysis by capillary zone electrophoresis with on-column transient isotachophoretic preconcentration


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Hydrogen ion buffers.
N E Good et al.
Methods in enzymology, 24, 53-68 (1972-01-01)
F Foret et al.
Electrophoresis, 14(5-6), 417-428 (1993-05-01)
The qualitative and quantitative aspects of transient isotachophoretic (ITP) sample preconcentration in the capillary zone electrophoretic analysis of protein samples have been demonstrated. By the proper selection of components of the background electrolyte and/or additives to the sample solution, two
A Fauvel et al.
Journal of pharmaceutical sciences, 73(6), 784-787 (1984-06-01)
Hemoglobin was freeze-dried in the presence of salts of EDTA, sulfonic acids used as buffers, or derivatives of pantothenic acid. At 0.25 M most of the compounds effectively inhibited the formation of methemoglobin. The various model compounds used (sodium zinc