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Glycolic acid

Glycolic acid Structure
CAS No.
79-14-1
Chemical Name:
Glycolic acid
Synonyms
2-HYDROXYACETIC ACID;GLYCOLATE;glycolic;HYDROXYACETIC ACID;HOCH2COOH;GLYCOLLIC ACID;Glycolic acid 70%;GLYCOLIC ACID SIGMAULTRA;glycolate (hydroxyacetate);GLYCOLIC ACID, HIGH PURITY, 70 WT.% SOLU TION IN WATER
CBNumber:
CB9463563
Molecular Formula:
C2H4O3
Molecular Weight:
76.05
MOL File:
79-14-1.mol
MSDS File:
SDS
Modify Date:
2024/8/8 13:40:43

Glycolic acid Properties

Melting point 75-80 °C (lit.)
Boiling point 112 °C
Density 1.25 g/mL at 25 °C
vapor pressure 10.8 hPa (80 °C)
refractive index n20/D 1.424
Flash point 112°C
storage temp. Store below +30°C.
solubility H2O: 0.1 g/mL, clear
form Solution
pka 3.83(at 25℃)
color White to off-white
PH 2 (50g/l, H2O, 20℃)
Odor at 100.00 %. odorless very mild buttery
Odor Type buttery
Water Solubility SOLUBLE
Sensitive Hygroscopic
Merck 14,4498
BRN 1209322
Stability Stable. Incompatible with bases, oxidizing agents and reducing agents.
InChIKey AEMRFAOFKBGASW-UHFFFAOYSA-N
LogP -1.07 at 20℃
CAS DataBase Reference 79-14-1(CAS DataBase Reference)
NIST Chemistry Reference Acetic acid, hydroxy-(79-14-1)
EPA Substance Registry System Glycolic acid (79-14-1)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS05,GHS07
Signal word  Danger
Hazard statements  H314-H332
Precautionary statements  P260-P271-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338
Hazard Codes  C
Risk Statements  34-22-20
Safety Statements  26-36/37/39-45-23
RIDADR  UN 3265 8/PG 3
WGK Germany  1
RTECS  MC5250000
TSCA  Yes
HS Code  2918 19 98
HazardClass  8
PackingGroup  II
Toxicity LD50 orally in rats: 1.95 g/kg, H. F. Smyth et al., J. Ind. Hyg. Toxicol. 23, 259 (1941)
NFPA 704
0
3 0

Glycolic acid price More Price(43)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) G8284 Glycolic acid BioXtra, ≥98.0% (titration) 79-14-1 10MG ₹1894.38 2022-06-14 Buy
Sigma-Aldrich(India) G8284 Glycolic acid BioXtra, ≥98.0% (titration) 79-14-1 25G ₹3236.68 2022-06-14 Buy
Sigma-Aldrich(India) PHR1427 Glycolic Acid Pharmaceutical Secondary Standard; Certified Reference Material 79-14-1 1G ₹8281.13 2022-06-14 Buy
Sigma-Aldrich(India) G8284 Glycolic acid BioXtra, ≥98.0% (titration) 79-14-1 100G ₹9233.73 2022-06-14 Buy
Sigma-Aldrich(India) G8284 Glycolic acid BioXtra, ≥98.0% (titration) 79-14-1 500G ₹26283.1 2022-06-14 Buy
Product number Packaging Price Buy
G8284 10MG ₹1894.38 Buy
G8284 25G ₹3236.68 Buy
PHR1427 1G ₹8281.13 Buy
G8284 100G ₹9233.73 Buy
G8284 500G ₹26283.1 Buy

Glycolic acid Chemical Properties,Uses,Production

Chemical Properties

Glycolic acid, CH20HCOOH, also known as hydroxyacetic acid, is composed of colorless deliquescent leaflets that decompose at approximately 78° C (172 OF). It is soluble in water,alcohol,and ether.Glycolic acid is used in dyeing, tanning, electropolishing,and in foodstuffs. It is produced by oxidizing glycol with dilute nitric acid.

Uses

glycolic acid (hydroxyacetic acid) reduces corenocyte cohesion and corneum layer thickening where an excess buildup of dead skin cells can be associated with many common skin problems, such as acne, dry and severely dry skin, and wrinkles. glycolic acid acts by dissolving the internal cellular cement responsible for abnormal keratinization, facilitating the sloughing of dead skin cells. It also improves skin hydration by enhancing moisture uptake as well as increasing the skin’s ability to bind water. This occurs in the cellular cement through an activation of glycolic acid and the skin’s own hyaluronic acid content. Hyaluronic acid is known to retain an impressive amount of moisture and this capacity is enhanced by glycolic acid. As a result, the skin’s own ability to raise its moisture content is increased. glycolic acid is the simplest alpha hydroxyacid (AHA). It is also the AHA that scientists and formulators believe has greater penetration potential largely due to its smaller molecular weight. It is mildly irritating to the skin and mucous membranes if the formulation contains a high glycolic acid concentration and/ or a low pH. glycolic acid proves beneficial for acne-prone skin as it helps keep pores clear of excess keratinocytes. It is also used for diminishing the signs of age spots, as well as actinic keratosis. However, glycolic acid is most popularly employed in anti-aging cosmetics because of its hydrating, moisturizing, and skin-normalizing abilities, leading to a reduction in the appearance of fine lines and wrinkles. Regardless of the G skin type, glycolic acid use is associated with softer, smoother, healthier, and younger looking skin. glycolic acid is naturally found in sugarcane but synthetic versions are most often used in cosmetic formulations.

Definition

ChEBI: A 2-hydroxy monocarboxylic acid that is acetic acid where the methyl group has been hydroxylated.

Preparation

There are different preparation methods to synthesize glycolic acid. However, the most common method is the catalyzed reaction of formaldehyde with synthesis gas, which costs less. It can be prepared when chloroacetic acid reacts with sodium hydroxide and undergoes re-acidification. Electrolytic reduction of oxalic acid also could synthesize this compound. Glycolic acid can be separated from natural sources like sugarcane, sugar beets, pineapple, cantaloupe, and unripe grapes. It can be prepared by hydrolyzing the cyanohydrin that is derived from formaldehyde.

benefits

Glycolic acid addresses skin issues by exfoliating dead skin cells that accumulate on the surface of the epidermis and contribute to dull, discolored, and uneven looking skin.

Side effects

Common side effects of Glycolic acid include dry skin, erythema (skin redness), burning sensation, itching, skin irritation, and skin rash. It can make the skin more sensitive in the sunlight, hence always use sunscreen and protective clothing before you step outdoors.

Source

Glycolic acid is widespread in nature and can be separated from natural sources like sugarcane, sugar beets, pineapple, cantaloupe, and unripe grapes.

Purification Methods

Crystallise it from diethyl ether. [Beilstein 3 IV 571.]

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