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Merck

410977

Sigma-Aldrich

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
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:

Pricing and availability is not currently available.

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

SMILES string

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

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1 of 4

This Item
576581723401732028
assay

97% (CP)

assay

-

assay

97% (CP)

assay

97% (CP)

mass shift

M+1

mass shift

M+1

mass shift

M+1

mass shift

M+4

form

gas

form

-

form

liquid

form

liquid

bp

6 °C (lit.)

bp

6 °C (lit.)

bp

69-71 °C/0.4 mmHg (lit.)

bp

246-248 °C (lit.)

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Storage Class Code

8B - Non-combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), 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
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
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
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
Irradiation inactivation analysis of acetylcholinesterase and the effect of buffer salts.
D Parkinson et al.
Radiation research, 90(2), 252-259 (1982-05-01)

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