POLYGLYCOLIDE

Product Information

Molecular Formula:
(C2H4O3)n
Molecular Weight:
0
Description
Polyglycolide (PGA) along with polylactide may be used to prepare a biodegradable copolymer to be used as implantations. Fabrication of biopolymer/carbon nanotube composite has been reported using PGA fiber as one of the constituents of the composite. Modified porous PGA scaffolds has been fabricated.
Synonyms
BP-0700; PURASORB(R) PG; POLY(GLYCOLIC ACID); POLYGLYCOLIDE; POLYGLYCOLLIC ACID; hydroxy-aceticacihomopolymer
IUPAC Name
2-hydroxyacetic acid
Canonical SMILES
C(C(=O)O)O
InChI
InChI=1S/C2H4O3/c3-1-2(4)5/h3H,1H2,(H,4,5)
InChI Key
AEMRFAOFKBGASW-UHFFFAOYSA-N
Boiling Point
100 °C
Melting Point
78-80 °C (alpha-modification)
Flash Point
Not applicable
Density
1.53 g/mL at 25 °C(lit.)
Solubility
In water, 1X10+6 mg/L at 25 °C (est)
Appearance
Colorless, translucent solid;Solid glycolic acid forms colorless, monoclinic, prismatic crystals
Application
Used as a cheap organic acid to manufacture adhesives; to dye, print, and crease-proof textiles; to clean metals, water wells, and dairy equipment; and to delime hides and process furs; Also used in leather dyeing, adhesives, electroplating, pH control, copper pickling, printed wire board flux, oil well acidification, biodegradable polymers, soldering compounds, iron chelating, chemical milling, etching lithographic plates, and dermatology; Active product registrations for uses in cleaning products.
Storage
2-8°C
Stability
Stable under recommended storage conditions.
LogP
log Kow = -1.11
Vapor Pressure
0.02 [mmHg]
Henry's Law Constant
8.5X10-8 atm-cu m/mol at 25 °C (est)
Decomposition
Hazardous decomposition products formed under fire conditions. - Carbon oxides
Dissociation Constants
3.83
Odor
Odorless

Safety Information

Handling
Eyeshields, Gloves, type N95 (US)

Computed Properties

XLogP3
-1.1
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
3
Rotatable Bond Count
1
Exact Mass
76.016043985 g/mol
Monoisotopic Mass
76.016043985 g/mol
Topological Polar Surface Area
57.5Ų
Heavy Atom Count
5
Formal Charge
0
Complexity
40.2
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-110028627-A Carboxymethyl cellulose graft copolymer and application thereof 2019-03-06
CN-106905488-A A kind of preparation method of many carboxy starch composite high water absorption resins 2017-04-12
CN-106905488-B A kind of preparation method of more carboxy starch composite high water absorption resins 2017-04-12
CN-110382553-A Amphiphilic polysaccharide derivates and composition comprising it 2016-12-16
CN-109312003-A Detergent composition 2016-06-13
CN-109312268-A Detergent composition 2016-06-13
TW-201708653-A Improved device and method 2015-06-01
US-2016200741-A1 Novel indazoles for the treatment and prophylaxis of respiratory syncytial virus infection 2015-01-09
CN-104448742-A High-performance anti-static filament reinforced polylactic acid composite material and preparation method thereof 2014-12-01
CN-104448742-B High performance antistatic long fiber reinforcement lactic acid composite material and preparation method thereof 2014-12-01

Literatures

PMID Publication Date Title Journal
33688722 2021-03-19 Covalent Inactivation of Mycobacterium tuberculosis Isocitrate Lyase by cis-2,3-Epoxy-Succinic Acid ACS chemical biology
33358762 2021-03-01 The EyeIRR-IS assay: Development and evaluation of an in vitro assay to measure the eye irritation sub-categorization of liquid chemicals Toxicology in vitro : an international journal published in association with BIBRA
32979392 2020-11-15 The effects of aliphatic alcohols and related acid metabolites in zebrafish embryos - correlations with rat developmental toxicity and with effects in advanced life stages in fish Toxicology and applied pharmacology
31711903 2020-01-01 Exposure-based assessment of chemical teratogenicity using morphogenetic aggregates of human embryonic stem cells Reproductive toxicology (Elmsford, N.Y.)
29953848 2018-08-25 Mechanistic-based non-animal assessment of eye toxicity: Inflammatory profile of human keratinocytes cells after exposure to eye damage/irritant agents Chemico-biological interactions
22975400 2012-12-01 Large-surface mesoporous TiO2 nanoparticles: synthesis, growth and photocatalytic performance Journal of colloid and interface science
23084901 2012-12-01 Prohormone-substrate peptide sequence recognition by peptidylglycine α-amidating monooxygenase and its reflection in increased glycolate inhibitor potency Bioorganic & medicinal chemistry letters
22137963 2012-11-01 Advanced bacterial polyhydroxyalkanoates: towards a versatile and sustainable platform for unnatural tailor-made polyesters Biotechnology advances
22925453 2012-11-01 Inside the alkalinity engine: the role of electron donors in the organomineralization potential of sulfate-reducing bacteria Geobiology
23044998 2012-11-01 Review: ototoxic characteristics of platinum antitumor drugs Anatomical record (Hoboken, N.J. : 2007)
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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