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2-(2-Methoxyethoxy)acetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 16024-56-9 Structure
  • Basic information

    1. Product Name: 2-(2-Methoxyethoxy)acetic acid
    2. Synonyms: TIMTEC-BB SBB008497;3,6-DIOXAHEPTANOIC ACID;2-(2-METHOXYETHOXY)ACETIC ACID;(2-methoxyethoxy)acetic acid;2-(2-METHOXYETHOXY)ACETIC ACID, TECH.;2-(2-Methoxyethoxy)Acetic;o-(2-methoxyethyl)glycolic acid;(2-Methoxyethoxy)essigsure
    3. CAS NO:16024-56-9
    4. Molecular Formula: C5H10O4
    5. Molecular Weight: 134.13
    6. EINECS: 240-161-6
    7. Product Categories: Heterocyclic Compounds
    8. Mol File: 16024-56-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 245-250 °C(lit.)
    3. Flash Point: >230 °F
    4. Appearance: /
    5. Density: 1.18 g/mL at 25 °C(lit.)
    6. Vapor Pressure: 0.00651mmHg at 25°C
    7. Refractive Index: n20/D 1.436(lit.)
    8. Storage Temp.: Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. PKA: 3.40±0.10(Predicted)
    11. Water Solubility: Fully miscible in water.
    12. BRN: 1753567
    13. CAS DataBase Reference: 2-(2-Methoxyethoxy)acetic acid(CAS DataBase Reference)
    14. NIST Chemistry Reference: 2-(2-Methoxyethoxy)acetic acid(16024-56-9)
    15. EPA Substance Registry System: 2-(2-Methoxyethoxy)acetic acid(16024-56-9)
  • Safety Data

    1. Hazard Codes: C
    2. Statements: 34
    3. Safety Statements: 26-36/37/39-45
    4. RIDADR: UN 3265 8/PG 2
    5. WGK Germany: 1
    6. RTECS:
    7. HazardClass: 8
    8. PackingGroup: II
    9. Hazardous Substances Data: 16024-56-9(Hazardous Substances Data)

16024-56-9 Usage

Chemical Properties

Colorless to pale yellow liquid

Check Digit Verification of cas no

The CAS Registry Mumber 16024-56-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,2 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16024-56:
(7*1)+(6*6)+(5*0)+(4*2)+(3*4)+(2*5)+(1*6)=79
79 % 10 = 9
So 16024-56-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H10O4/c1-8-2-3-9-4-5(6)7/h2-4H2,1H3,(H,6,7)/p-1

16024-56-9 Well-known Company Product Price

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  • Alfa Aesar

  • (L20090)  2-(2-Methoxyethoxy)acetic acid, 98%   

  • 16024-56-9

  • 5g

  • 618.0CNY

  • Detail
  • Alfa Aesar

  • (L20090)  2-(2-Methoxyethoxy)acetic acid, 98%   

  • 16024-56-9

  • 25g

  • 2385.0CNY

  • Detail
  • Aldrich

  • (407011)  2-(2-Methoxyethoxy)aceticacid  technical grade

  • 16024-56-9

  • 407011-250ML

  • 2,713.23CNY

  • Detail
  • Aldrich

  • (407011)  2-(2-Methoxyethoxy)aceticacid  technical grade

  • 16024-56-9

  • 407011-1L

  • 8,096.40CNY

  • Detail

16024-56-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-Methoxyethoxy)acetic acid

1.2 Other means of identification

Product number -
Other names 2-(2-Methoxyethoxy)Acetic Acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:16024-56-9 SDS

16024-56-9Relevant articles and documents

Electroorganic synthesis in oil-in-water (O/W) nanoemulsion: TEMPO-mediated electrooxidation of amphiphilic alcohols in water

Kuroboshi, Manabu,Yoshida, Tomonori,Oshitani, Jun,Goto, Kuniaki,Tanaka, Hideo

, p. 7177 - 7185 (2009)

Oil-in-water nanoemulsion which consisted of TEMPO, amphiphilic alcohols, and water offered unique reaction environments for electrooxidation of the alcohols to give the corresponding carboxylic acids in good to excellent yields.

NOVEL TRITERPENE DERIVATIVES AS HIV INHIBITORS

-

Page/Page column 51, (2020/08/28)

The present invention relates to novel triterpene derivatives of formula (I); and pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, and ring are as defined herein. The invention also relates to novel triterpene derivatives, related compounds, and pharmaceutical compositions useful for the therapeutic treatment of viral diseases and particularly HIV mediated diseases.

BENZODICYCLOALKANE DERIVATIVE, PREPARATION METHOD AND USE THEREOF

-

Paragraph 0154; 0348; 0352; 0436; 0438, (2019/06/19)

It is provided herein a benzobicycloalkane derivative, and a preparation method and use thereof. In particular, it is provided herein a compound of Formula (I), or a pharmaceutically acceptable salt, stereoisomer or solvate thereof, a preparation method, and a use thereof in preparation of drugs for treating pain.

OPIOID AGONISTS AND USES THEREOF

-

Paragraph 00261, (2015/06/11)

Provided are compounds, including those of Formula I; and pharmaceutically acceptable salts and solvates thereof. The compounds described herein relate to and/or have application(s) in (among others) the fields of drug discovery, pharmacotherapy, physiology, organic chemistry and polymer chemistry.

Ceria supported gold-platinum catalysts for the selective oxidation of alkyl ethoxylates

Heidkamp, Katharina,Aytemir, Memet,Vorlop, Klaus-Dieter,Pruesse, Ulf

, p. 2984 - 2992 (2013/11/06)

This work covers the development of a ceria based AuPt catalyst for the selective aerobic oxidation of alkyl ethoxylates to their corresponding carboxylic acids. By optimizing metal loading and the Au to Pt ratio the activity of the catalyst could be increased significantly, while maintaining total selectivity. Although the choice of ceria as a support helped to suppress intermediate metal leaching, the catalyst still showed poor long-term stability in repeated batches. The cause for deactivation could finally be identified by TPR studies as over-oxidation. These suspicions were confirmed by a long-term stability study in continuous-mode. It proved to be possible to deactivate the catalyst on purpose by employing unfavourable oxidising reaction conditions, i.e. low substrate concentrations and excess oxygen. By avoiding such unfavourable conditions either in continuous-flow mode or in repeated batches, the long-term stability of the catalyst increased tremendously. A substrate screening of various ethoxylates showed that the catalyst was very well-suited to selectively oxidize a wide range of alkyl ethoxylates.

Chromium(VI) oxide oxidation of non-ethoxylated and ethoxylated alcohols for determination by electrospray ionization mass spectrometry

Beneito-Cambra, Miriam,Bernabe-Zafon, Virginia,Simo-Alfonso, Ernesto F.,Ramis-Ramos, Guillermo

experimental part, p. 2093 - 2100 (2011/11/06)

A new derivatization procedure to increase the sensitivity of electrospray ionization mass spectrometry (ESI-MS) to non-ethoxylated and ethoxylated alcohols was investigated. The analytes were oxidized with chromium(VI) oxide and the resulting carboxylic and ethoxy-carboxylic acids were isolated by extraction with ethyl acetate; the extracts were alkalinized and infused into the ESI-MS system working in the negative-ion mode. The yields of the combined oxidation-extraction were ca. 100% for non-ethoxylated fatty alcohols dissolved in acetone and they decreased moderately in samples containing increasing amounts of water (e.g., a 75% yield was obtained with 50% water). Ethoxylated alcohols with more than two ethylene oxide units resulted in yields of ca. 60%. Low limits of detection (LODs) were obtained when the procedure was applied to the analysis of body- care products and cosmetics containing fatty alcohols, e.g., in a varicose-vein cream, the LODs were 25 μ cetyl alcohol and 7.5 μ stearyl alcohol (detected as palmitic acid and stearic acid, respectively) per gram of sample. High molecular mass alcohols were also detected in seawater after pre- concentration by solid-phase extraction. Thus, the proposed method is particularly valuable for use in industrial samples having complex matrices and in environmental samples and it is competitive with other methods for the analysis of trace amounts of fatty alcohols.

Electroorganic synthesis in oil-in-water nanoemulsion: TEMPO-mediated electrooxidation of amphiphilic alcohols in water

Yoshida, Tomonori,Kuroboshi, Manabu,Oshitani, Jun,Gotoh, Kuniaki,Tanaka, Hideo

, p. 2691 - 2694 (2008/02/12)

Oil-in-water nanoemulsions, consisting of TEMPO, amphiphilic alcohols, and water, offer unique reaction environments for electrooxidation of the alcohols to give the corresponding carboxylic acids in good to excellent yields. Georg Thieme Verlag Stuttgart.

Permeable, water soluble, non-irritating prodrugs of chemotherapeutic agents with oxaalkanoic acids

-

, (2008/06/13)

The present invention relates to the field of prodrugs of chemotherapeutic agents and method of use thereof.

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