mPEG3-acetic acid

 CAS No.: 16024-60-5  Cat No.: BP-501475  Purity: >97% 4.5  

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

mPEG3-acetic acid

Structure of 16024-60-5

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Molecular Formula
C9H18O6
Molecular Weight
222.24
Appearance
Colorless or Light Yellowish Liquid

* For research and manufacturing use only. Not for human or clinical use.

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Popular Publications Citing BOC Sciences Products
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.
IUPACName
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
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
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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