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    2. Fine Chemicals: Catalsts and Auxiliary Agents

      Home - Products List - Fine Chemicals: Catalsts and Auxiliary Agents

      Glycolic acid

      • Product Name: Glycolic acid
      • CAS: 79-14-1
      • Purity:
      • Appearance: Light yellow to amber liquid

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      Factory supply good quality Glycolic acid 79-14-1 with stock

      • Molecular Formula:C2H4O3
      • Molecular Weight:76.052
      • Appearance/Colour:Light yellow to amber liquid 
      • Vapor Pressure:0.001mmHg at 25°C 
      • Melting Point:75-80 °C(lit.) 
      • Refractive Index:n20/D 1.424  
      • Boiling Point:265.6 °C at 760 mmHg 
      • Flash Point:128.7 °C 
      • PSA:57.53000 
      • Density:1.416 g/cm3 
      • LogP:-0.93670 

      Glycolic acid(Cas 79-14-1) Usage

      Industrial and Commercial Uses

      Widely used in various industries, including pH control, cleaning agents, metal processing, textile dyeing and tanning, adhesives, and water treatment.
      Used in acidic cleansing agents, dairy and industrial cleaning agents, and inhibits the growth of iron-oxidizing bacteria.
      Applied in metal processing for pickling, cleaning, chemical milling, and electroplating, as well as in textile dyeing, printing, and creaseproofing.
      Commercially available as a technical grade 70% aqueous solution, a 57% aqueous solution, or a 100% crystalline solid.

      Medical and Cosmetic Applications

      Utilized in the pharmaceutical industry as a skin care agent, and in the food industry as a flavor and preservative.
      Included in cosmetics as a skin-conditioning additive and humectant to help retain moisture.
      Marketed for cosmetic products and household cleaning agents, with a growing market size expected to reach US$415.0 million by 2024.

      Biomedical Applications

      Used in medical applications for its ability to convert to biodegradable polymers like polyglycolic acid (PGA) and copolymers such as polylactic-co-glycolic acid (PLGA). PLGA is used in various medical applications due to its good mechanical properties.

      Regulatory Status

      Previously regulated as an antimicrobial pesticide under the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA), but its use as a pesticide has been cancelled.
      Still regulated by FIFRA as an inert ingredient, categorized under List 3, inerts of unknown toxicity, with a PC code assigned by the EPA.

      General Description

      Glycolic acid is a type of alpha hydroxy acid (AHA) derived from sugar cane. It is a colorless, odorless, and water-soluble chemical that is commonly used in skin care products. Glycolic acid is known for its exfoliating properties, as it works by breaking down the bonds between dead skin cells, promoting the shedding of the outer layer of the skin. This process helps to improve skin texture, reduce the appearance of fine lines and wrinkles, and even out skin tone. Additionally, glycolic acid can also help to unclog pores and reduce acne. It is a popular ingredient in chemical peels and other professional skin treatments, as well as in over-the-counter skincare products such as cleansers, toners, and serums. While glycolic acid can be beneficial for many skin types, it is important to use it cautiously and always wear sunscreen when using products containing this ingredient, as it can increase skin sensitivity to the sun.

      InChI:InChI=1/C2H4O3/c3-1-2(4)5/h3H,1H2,(H,4,5)/p-1

      79-14-1 Relevant articles

      Gas Evolution Oscillators. 2. A Reexamination of Formic Acid Dehydration

      Smith, Kenneth W.,Noyes, Richard M.,Bowers, Peter G.

      , p. 1514 - 1519 (1983)

      At formic acid concentrations of about 0...

      Glycolic acid production using ethylene glycol-oxidizing microorganisms

      Kataoka, Michihiko,Sasaki, Mie,Hidalgo, Aklani-Rose G.D.,Nakano, Michiko,Shimizu, Sakayu

      , p. 2265 - 2270 (2001)

      Screening for microorganisms oxidizing e...

      Glycolic acid formation in Chlorella.

      WARBURG,KRIPPAHL

      , (1960)

      -

      Theoretical study of Al(iii)-catalyzed conversion of glyoxal to glycolic acid: Dual activated 1,2-hydride shift mechanism by protonated Al(OH) 3 species

      Ohshima, Takashi,Yamamoto, Yoshihiro,Takaki, Usaji,Inoue, Yoshihisa,Saeki, Takuya,Itou, Kenji,Maegawa, Yusuke,Iwasaki, Takanori,Mashima, Kazushi

      , p. 2688 - 2690 (2009)

      Density functional theory calculations d...

      Facilitated series electrochemical hydrogenation of oxalic acid to glycolic acid using TiO2 nanotubes

      Im, Sunmi,Park, Yiseul,Saad, Sarwar

      , (2022/01/11)

      In this study, the electrochemical reduc...

      Electrochemical oxidation of diclofenac on CNT and M/CNT modified electrodes

      Ferreira, M.,Figueiredo, J. L.,Fonseca, A. M.,Güney, S.,Ku?niarska-Biernacka, I.,Neves, I. C.,Parpot, P.,Pereira, M. F. R.,Soares, O. S. G. P.

      , p. 12622 - 12633 (2021/07/25)

      The electrochemical oxidation of diclofe...

      PROCESSES FOR PREPARING ALDARIC, ALDONIC, AND URONIC ACIDS

      -

      Paragraph 0113-0116, (2021/05/29)

      Various processes for preparing aldaric ...

      Experimental and kinetic study of the conversion of waste starch into glycolic acid over phosphomolybdic acid

      Dai, Hongqi,Qiao, Yongzhen,Wang, Xiu

      , p. 30961 - 30970 (2021/11/19)

      The starch used to enhance the paper sur...

      79-14-1 Process route

      L-Tartaric acid
      87-69-4,138508-61-9

      L-Tartaric acid

      carbon dioxide
      124-38-9,18923-20-1

      carbon dioxide

      sulfuric acid
      7664-93-9

      sulfuric acid

      glycolic Acid
      79-14-1

      glycolic Acid

      DL-tartaric acid
      133-37-9,138508-61-9

      DL-tartaric acid

      2-oxo-propionic acid
      127-17-3

      2-oxo-propionic acid

      Conditions
      Conditions Yield
      rhodamine B
      81-88-9

      rhodamine B

      phenylacetic acid
      103-82-2

      phenylacetic acid

      glycolic Acid
      79-14-1

      glycolic Acid

      LACTIC ACID
      849585-22-4,106989-11-1,26811-96-1,31587-11-8,26100-51-6

      LACTIC ACID

      propylene glycol
      57-55-6,63625-56-9

      propylene glycol

      cyclohexen-1-ol
      4065-81-0

      cyclohexen-1-ol

      1.3-butanediol
      18826-95-4,107-88-0

      1.3-butanediol

      4-Methyl-1-pentanol
      626-89-1

      4-Methyl-1-pentanol

      terephthalic acid
      100-21-0

      terephthalic acid

      Phthalic acid dibutyl ester
      84-74-2

      Phthalic acid dibutyl ester

      2-Phenylbutyric acid
      90-27-7

      2-Phenylbutyric acid

      cyclohexanol
      108-93-0

      cyclohexanol

      Conditions
      Conditions Yield
      for 0.5h; pH=5; UV-irradiation; Darkness;

      79-14-1 Upstream products

      • 56-23-5
        56-23-5

        tetrachloromethane

      • 53834-50-7
        53834-50-7

        (Z)-1,2-dichloro-3-phenyl-2-propene

      • 502-97-6
        502-97-6

        glycolide

      • 50-00-0
        50-00-0

        formaldehyd

      79-14-1 Downstream products

      • 6478-80-4
        6478-80-4

        5,6-dichloro-2-hydroxymethyl-1H-benzimidazole

      • 87-51-4
        87-51-4

        indole-3-acetic acid

      • 90357-58-7
        90357-58-7

        n-propyl 2-hydroxyacetate

      • 624-55-5
        624-55-5

        glycolic acid-(2-ethoxy-ethyl ester)

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