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Glycolic Acid, Crystal, Reagent

Catalog NumberACM79141-1

CAS Number79-14-1

CategoryPolymers

Glycolic Acid, Crystal, Reagent
Description
DryPowder; Liquid; PelletsLargeCrystals;Solid;COLOURLESS HYGROSCOPIC CRYSTALS.
IUPAC Name
2-hydroxyacetic acid
Molecular Weight
76.05g/mol
Molecular Formula
C2H4O3;HOCH2COOH;C2H4O3
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
79.5 °C;78-80 °C (alpha-modification); 63 °C (beta-modification, metastable);75-80°C;80 °C
Density
1.49 at 25 °C/4 °C;Relative density (water = 1): 1.49
Solubility
In water, 1X10+6 mg/L at 25 °C (est);Soluble in ethanol, ethyl ether;Soluble in methanol, acetone, acetic acid;Solubility in water: very good
Application
Glycolic Acid, Crystal, Reagent serves a versatile purpose across various industries, primarily in skincare. As the smallest alpha-hydroxy acid (AHA), its molecular structure allows for deep penetration into the skin, making it highly effective in exfoliating and enhancing skin hydration. It dissolves the cellular cement responsible for excessive keratinization, promoting the sloughing of dead skin cells and reducing common skin issues like acne, dry skin, and wrinkles. Its ability to enhance moisture uptake and improve skin's water binding capacity further elevates its role in skincare, leading to softer, smoother, and younger-looking skin. Beyond cosmetics, glycolic acid is utilized in the textile industry for dyeing and tanning, as a flavoring agent in food processing, and in pharmaceuticals. Additionally, it is integrated into emulsion polymers, solvents, and ink additives to improve flow properties and add gloss. Glycolic acid is also a key intermediate in organic synthesis, including reactions like oxidative-reduction, esterification, and polymerization, making it indispensable in both industrial and cosmetic applications.
Color/Form
Colorless, translucent solid;Solid glycolic acid forms colorless, monoclinic, prismatic crystals.;Orthorhombic needles from water; leaves from diethyl ether
Complexity
40.2
Corrosivity
Corrosive
Covalently-Bonded Unit Count
1
EC Number
201-180-5;217-693-2;247-326-1
Exact Mass
76.016044g/mol
Formal Charge
0
Heavy Atom Count
5
ICSC Number
1537
Log P
-1.11 (LogP);log Kow = -1.11;-1.11;-1.11
MeSH Entry Terms
glycolate;glycolic acid;glycolic acid, 1-(14)C-labeled;glycolic acid, 2-(14)C-labeled;glycolic acid, calcium salt;glycolic acid, monoammonium salt;glycolic acid, monolithium salt;glycolic acid, monopotassium salt;glycolic acid, monosodium salt;glycolic acid, potassium salt;hydroxyacetic acid;potassium glycolate
Monoisotopic Mass
76.016044g/mol
NSC Number
166
Odor
Odorless
Other Experimental
BP: decomposes;MP: 79.5 °C;Hygroscopic;Heat of combustion: 697.1kJ/mole; heat of solution: -11.5 kJ/mole;Light, straw-colored lliquid, odor like burnt sugar; density: 1.27; mp: 10 °C /Commercial 70% solution/;When heated to decomposition it emits acrid smoke and irritating fumes.;Henry's Law constant = 8.5X10-8 atm-cu m/mol at 25 °C (est);Hydroxyl radical reaction rate constant = 3.11X10-12 cu cm/molecule-sec at 25 °C (est)
Rotatable Bond Count
1
RTECS Number
MC5250000
Stability
Stable under recommended storage conditions.
UNII
0WT12SX38S
UN Number
3261
Vapor Density
Relative vapor density (air = 1): 2.6
Vapor Pressure
0.02 mmHg;2.0X10-2 mm Hg at 25 °C (extrapolated)
XLogP3
-1.1
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