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83263

Sigma-Aldrich

BICINE buffer Solution

BioUltra, for molecular biology, 1 M in H2O

Sinónimos:

N,N-Bis(2-hydroxyethyl)glycine

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About This Item

Fórmula empírica (notación de Hill):
C6H13NO4
Número de CAS:
150-25-4
Peso molecular:
163.17
Beilstein/REAXYS Number:
1769362
MDL number:
MFCD00004295
UNSPSC Code:
12161700
eCl@ss:
32129211
PubChem Substance ID:
24888105

grade

for molecular biology

product line

BioUltra

concentration

1 M in H2O

impurities

DNases, none detected
 RNases, none detected
 phosphatases, none detected
 proteases, none detected

pH

5.0±0.2

density

1.05 g/mL at 20 °C

λ

neat

UV absorption

λ: 260 nm Amax: <0.07
λ: 280 nm Amax: <0.04

suitability

in accordance for filter test

SMILES string

OCCN(CCO)CC(O)=O

Storage Class

12 - Non Combustible Liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves

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S Ito et al.
Clinica chimica acta; international journal of clinical chemistry, 115(2), 135-144 (1981-09-10)
Serum guanase activity has been considered as a possible specific indicator of hepatocellular diseases. However, no suitable method is available for routine clinical determination of serum guanase activity. Conventional assay methods are troublesome and inaccurate, since guanine and 8-azaguanine, the
Raewyn M Town et al.
The journal of physical chemistry. A, 112(12), 2563-2571 (2008-03-04)
The impact of ligand protonation on the complexation kinetics of higher-order complexes is quantitatively described. The theory is formulated on the basis of the usual situation for metal complex formation in aqueous systems in which the exchange of water for
Dominik Koszel et al.
Journal of enzyme inhibition and medicinal chemistry, 27(2), 167-173 (2011-06-04)
A series of bis-N,N-(2-hydroxyethyl)glycine (bicine) derivatives, conjugated with an inhibitor of glucosamine-6-phosphate synthase, have been synthesized and their lipophilic and antifungal properties have been tested. The obtained compounds demonstrated higher lipophilicity than free inhibitor (FMDP) and, in consequence, an increased
Irradiation inactivation analysis of acetylcholinesterase and the effect of buffer salts.
D Parkinson et al.
Radiation research, 90(2), 252-259 (1982-05-01)
N R Vaidya et al.
Electrophoresis, 11(2), 156-161 (1990-02-01)
Using 2 or 3 simple Good zwitterionic buffers at a 16 or 18 mmol/L final column concentration of the mixture, natural pH gradients of 4 to 8 and 3 to 9.5, respectively, were generated in a liquid LKB column. The
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