mPEG3-acetic acid - CAS 16024-60-5

2,5,8,11-Tetraoxa-13-tridecanoic Acid (CAS# 16024-60-5 ) is a useful research chemical.

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Molecular Formula
C9H18O6
Molecular Weight
222.24

mPEG3-acetic acid

    • Specification
      • Purity
        >97%
        Appearance
        Colorless or Light Yellowish Liquid
        Storage
        Pure form, -20°C, 3 years; 4°C, 2 years; In solvent, -80°C, 6 months; -20°C, 1 month
        Shipping
        Room temperature in continental US; may vary elsewhere.
        IUPAC Name
        2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]acetic acid
        Synonyms
        2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]acetic acid; 2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]acetic acid
    • Properties
      • Boiling Point
        338.4±27.0 °C at 760 mmHg
        Density
        1.1±0.1 g/cm3
        InChI Key
        BCGLNCAVZDQPGE-UHFFFAOYSA-N
        InChI
        InChI=1S/C9H18O6/c1-12-2-3-13-4-5-14-6-7-15-8-9(10)11/h2-8H2,1H3,(H,10,11)
        Canonical SMILES
        COCCOCCOCCOCC(=O)O
    • Reference Reading
      • 1. Kinetics of hydroxyapatite dissolution in acetic, lactic, and phosphoric acid solutions
        H C Margolis, E C Moreno Calcif Tissue Int. 1992 Feb;50(2):137-43.doi: 10.1007/BF00298791.
        The present study was undertaken in an attempt to relate the kinetics of hydroxyapatite dissolution to solution parameters, under experimental conditions relevant to the dental caries process. Thus, the dissolution of hydroxyapatite was studied in acetic, lactic, and dilute phosphoric acid solutions having initial pH values from 4 to 6. Rates of dissolution and the corresponding degree of saturation with respect to hydroxyapatite were determined at various times throughout the dissolution process. Rates of dissolution of all solutions were found to decrease with increasing degree of solution saturation and were greater in solutions with lower initial values of pH. However, rates of dissolution in partially saturated phosphoric acid solutions (without added organic acid) were at least one order of magnitude lower than those observed in the organic acid buffers with the same initial pH, over the same range of saturation values. The data obtained are consistent with a surface-controlled dissolution model in which the rate of dissolution is dependent upon the degree of saturation and the sum of the activities of the acidic species in solution, i.e., phosphoric and organic acids. These results suggest that in order to assess the cariogenic potential of a given medium (e.g., plaque fluid), one must determine both the degree of saturation with respect to the dissolving mineral and the activities of acidic species in solution.
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