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Merck

77067

Supelco

Glycerin

analytical standard

Synonym(e):

1,2,3-Propantriol, Glycerin

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About This Item

Lineare Formel:
HOCH2CH(OH)CH2OH
CAS-Nummer:
Molekulargewicht:
92.09
Beilstein:
635685
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
85151701
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Dampfdichte

3.1 (vs air)

Dampfdruck

<1 mmHg ( 20 °C)

Assay

≥98.5% (GC)

Selbstzündungstemp.

698 °F

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Verunreinigungen

≤0.3% water

Brechungsindex

n20/D 1.474 (lit.)

bp

182 °C/20 mmHg (lit.)

mp (Schmelzpunkt)

20 °C (lit.)

Dichte

1.25 g/mL (lit.)

Anwendung(en)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

Format

neat

SMILES String

OCC(O)CO

InChI

1S/C3H8O3/c4-1-3(6)2-5/h3-6H,1-2H2

InChIKey

PEDCQBHIVMGVHV-UHFFFAOYSA-N

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Allgemeine Beschreibung

Glycerol is a simple polyol compound, which is obtained as a byproduct of soap and biodiesel industries.
Glycerol is odourless, colorless, viscous in nature, and exists as a sweet tasting liquid. It can be derived naturally as well as from petrochemical feedstock. Glycerol has a wide variety of applications, and is one of the most valuable and versatile chemical substances in nature. It can be used as an emollient, solvent, sweetening agent, in pharmaceutical formulations, cosmetics, foodstuffs and toiletries. It is very stable and can be easily stored under normal temperature; also it is non-irritating and has no adverse impact to the environment.
This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food. Find all available reference materials for compounds listed in 10/2011 here

Anwendung

Glycerol has been used as
  • a supplement during cell culture of Mycobacterium tuberculosis and Mycobacterium avium.
  • a fuel during designing enzymatic biofuel cell.
  • a liquid composite matrix with 4-HCCA and 3-amino­quinoline for analysis of neutral and acidic glycans.
  • a matrix for fast atom bombardment MS.
  • may be employed as liquid matrix for the quantification studies by MALDI (Matrix-assisted laser desorption/ionization mass spectrometry) analysis.
Glycerol may be used as a reference standard in the determination of glycerol in samples of beer using gas liquid chromatography (GLC).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Biochem./physiol. Wirkung

Glycerol is hygroscopic in nature and is soluble in water owing to its three hydrophilic alcoholic hydroxyl groups. It can form both inter- and intramolecular hydrogen bonds, making it a very flexible molecule. The physiologic effect of glycerine is due to cell-mediated immunity, increased IgG production and increased histamine release.

Empfohlene Produkte

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 1

Flammpunkt (°F)

390.2 °F - Pensky-Martens closed cup

Flammpunkt (°C)

199 °C - Pensky-Martens closed cup


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Analysenzertifikate (COA)

Lot/Batch Number

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Kunden haben sich ebenfalls angesehen

The Future of Glycerol (2010)
The quantitative determination of glycerol in beer by gas?liquid chromatography.
Parker E W and Richardson J P.
Journal of the Institute of Brewing, 76(2), 191-198 (1970)
Biofuels: Securing the Planet?s Future Energy Needs (2008)
B E Aronson et al.
Biochimica et biophysica acta, 1839(11), 1273-1282 (2014-06-01)
GATA4 is expressed in the proximal 85% of small intestine where it promotes a proximal intestinal ('jejunal') identity while repressing a distal intestinal ('ileal') identity, but its molecular mechanisms are unclear. Here, we tested the hypothesis that GATA4 promotes a
Guntram Borck et al.
Genome research, 25(2), 155-166 (2015-01-07)
RNA polymerase III (Pol III) synthesizes tRNAs and other small noncoding RNAs to regulate protein synthesis. Dysregulation of Pol III transcription has been linked to cancer, and germline mutations in genes encoding Pol III subunits or tRNA processing factors cause

Protokolle

99%; Glycerol, ≥99.5%; Tetraethylene glycol, 99%

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