49781
Glycerol solution
83.5-89.5% (T)
Synonym(s):
1,2,3-Propanetriol
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Linear Formula:
HOCH2CH(OH)CH2OH · aq
CAS Number:
Molecular Weight:
92.09 (anhydrous basis)
Beilstein:
635685
EC Number:
MDL number:
UNSPSC Code:
50161901
PubChem Substance ID:
NACRES:
NA.28
Recommended Products
Quality Level
Assay
83.5-89.5% (T)
form
viscous liquid
technique(s)
MALDI-MS: suitable
impurities
10.5-16.5% water
ign. residue
≤0.01% (as SO4)
bp
182 °C/20 mmHg (lit.)
density
1.252 g/mL at 25 °C (lit.)
SMILES string
OCC(O)CO
InChI
1S/C3H8O3/c4-1-3(6)2-5/h3-6H,1-2H2
InChI key
PEDCQBHIVMGVHV-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
General description
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.
Application
Glycerol solution has been used:
- in the preparation of blood mimicking fluid
- in epidermis mimicking films
- as a constituent of nuclei storage buffer
Biochem/physiol Actions
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 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.
Other Notes
Substrate for the assay of glycerokinase; glycerol dehydratase; glycerol oxidase
WGK
WGK 1
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Glycerol oxidase from Aspergillus japonicus.
T Uwajima et al.
Methods in enzymology, 89 Pt D, 243-248 (1982-01-01)
Automated end-to-end blood testing at the point-of-care: Integration of robotic phlebotomy with downstream sample processing
Balter ML, et al.
Technology, 1-8 (2018)
Glycerol dehydratase from Aerobacter aerogenes.
B C Johnson et al.
Methods in enzymology, 42, 315-323 (1975-01-01)
Multilayered tissue mimicking skin and vessel phantoms with tunable mechanical, optical, and acoustic properties
Chen AI, et al.
Medical Physics, 43(6), 3117-3131 (2016)
H.U. Bergmeyer, ed.
Methods of Enzymatic Analysis, 2, 216-216 (1983)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service