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Merck
CN

410977

Bicine sodium salt

40 wt. % in H2O

Synonym(s):

N,N-Bis(2-hydroxyethyl)glycine sodium salt

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About This Item

Linear Formula:
(HOCH2CH2)2NCH2CO2Na
CAS Number:
Molecular Weight:
185.15
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
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SMILES string

[Na+].OCCN(CCO)CC([O-])=O

concentration

40 wt. % in H2O

impurities

≤10% diethanolamine, sodium carbonate, sodium hydroxide and ammonium (total)

refractive index

n20/D 1.413

density

1.2 g/mL at 25 °C

pictograms

Corrosion

signalword

Danger

Hazard Classifications

Aquatic Chronic 3 - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B

Storage Class

8B - Non-combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

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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
Yoshiteru Seo et al.
Magnetic resonance in medicine, 65(4), 1005-1012 (2011-03-18)
The toxicity of free Mn(2+) is a bottleneck for the in vivo application of manganese ion enhanced MRI. To reduce free Mn(2+) concentration ([Mn(2+) ]), a low affinity chelate reagent: N,N-bis(2-hydroxyethyl)glycine (bicine) was used. Considering the conditional association constant of
S Ito et al.
The Histochemical journal, 16(5), 489-499 (1984-05-01)
Histochemical studies of human guanase (guanine deaminase) have seldom been undertaken, in part because of technical difficulties which result in heavy background staining. In this report, we describe a modified procedure in which the methodological inadequacies have been overcome. The
E Gopinath et al.
Proceedings of the National Academy of Sciences of the United States of America, 86(9), 3041-3044 (1989-05-01)
The nature and rate of reduction of Hg2+ to Hg0 by 1,5-dihydro-3,(3-sulfopropyl)lumiflavin (FIH2) in buffered aqueous solutions (pH 4.7) is dependent on the ligation of Hg2+. In the presence of N,N-bis(2-hydroxyethyl)glycine or when ligated to ethylenediaminetetraacetic acid, the reduction is
The myosin dimer: an intermediate in the self-assembly of the thick filament of vertebrate skeletal muscle.
J S Davis et al.
FEBS letters, 140(2), 293-297 (1982-04-19)

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