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C14E6 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 5157-04-0 Structure
  • Basic information

    1. Product Name: C14E6
    2. Synonyms: C14E6;HEXAETHYLENE GLYCOL MONOTETRADECYL ETHER;TETRADECYLHEXAGLYCOL;polyoxyethylene 6 myristyl ether;3,6,9,12,15,18-hexaoxadotriacontan-1-ol;hexaethyleneglycol mono-n-tetradecyl ether;C14E6, Tetradecylhexaglycol;17-(Tetradecyloxy)-3,6,9,12,15-pentaoxaheptadecane-1-ol
    3. CAS NO:5157-04-0
    4. Molecular Formula: C26H54O7
    5. Molecular Weight: 478.7
    6. EINECS: 225-930-6
    7. Product Categories: N/A
    8. Mol File: 5157-04-0.mol
  • Chemical Properties

    1. Melting Point: 32-33 °C
    2. Boiling Point: 544.7oC at 760mmHg
    3. Flash Point: 283.2oC
    4. Appearance: Solid
    5. Density: 0.97 g/cm3
    6. Vapor Pressure: 3.91E-14mmHg at 25°C
    7. Refractive Index: 1.457
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 14.36±0.10(Predicted)
    11. Stability: Stable.
    12. BRN: 1805220
    13. CAS DataBase Reference: C14E6(CAS DataBase Reference)
    14. NIST Chemistry Reference: C14E6(5157-04-0)
    15. EPA Substance Registry System: C14E6(5157-04-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: 22-24/25
    4. RIDADR: UN 3082 9/PG 3
    5. WGK Germany: 2
    6. RTECS:
    7. F: 3
    8. HazardClass: N/A
    9. PackingGroup: N/A
    10. Hazardous Substances Data: 5157-04-0(Hazardous Substances Data)

5157-04-0 Usage

Chemical Properties

Solid

Check Digit Verification of cas no

The CAS Registry Mumber 5157-04-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,5 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5157-04:
(6*5)+(5*1)+(4*5)+(3*7)+(2*0)+(1*4)=80
80 % 10 = 0
So 5157-04-0 is a valid CAS Registry Number.
InChI:InChI=1/C26H54O7/c1-2-3-4-5-6-7-8-9-10-11-12-13-15-28-17-19-30-21-23-32-25-26-33-24-22-31-20-18-29-16-14-27/h27H,2-26H2,1H3

5157-04-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-[2-[2-[2-(2-tetradecoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethanol

1.2 Other means of identification

Product number -
Other names 3,6,9,12,15,18-Hexaoxadotriacontan-1-ol

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:5157-04-0 SDS

5157-04-0Relevant articles and documents

Efficient concrete foam stabilizer and preparation method thereof

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Paragraph 0027; 0052-0053, (2021/07/17)

The invention discloses an efficient concrete foam stabilizer and a preparation method thereof, according to the efficient foam stabilizer, polyol is subjected to an esterification reaction to form ester bonds, and the ester bonds are connected with amphiphilic side chains, and the number of the amphiphilic side chains is 3-7; one end of the amphiphilic side chain is a hydrophobic chain segment, and the other end of the amphiphilic side chain is a hydrophilic unit; wherein the hydrophobic chain segment is an alkyl chain (R) with 8-14 carbons, and the hydrophilic unit is 2-10 ethylene oxide units. The efficient concrete foam stabilizer is a multi-chain type surfactant, and the multi-chain type surfactant is hydrolyzed under the alkaline condition to release an air-entraining type surfactant. The efficient concrete foam stabilizer has an excellent effect of stabilizing the air content of concrete, meanwhile, hardened concrete has a better pore structure, and the hardening strength of the concrete cannot be greatly influenced.

Combinatorial synthesis of PEG oligomer libraries

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Page/Page column 10, (2010/02/15)

A simple chain-extending approach was established for the scale-up of the monoprotected monodisperse PEG diol materials. Reactions of THP-(OCH2CH2)n—OMs (n=4, 8, 12) with a large excess of commercially available H—(OCH2CH2)n—OH (n=1-4) under basic conditions led to THP-(OCH2CH2)n—OH (n=5-15). Similarly, Me-(OCH2CH2)n—OH (n=4-11, 13) were prepared from Me-(OCH2CH2)n—OMs (n=3, 7, 11). For the chain elongation steps, 40-80% yields were achieved through extraction purification. PEG oligomer libraries I and II were generated in 50-95% overall yields by alkylation or acylation of THP-(OCH2CH2)n—OH (n=1-15) followed by deprotection. Alkylation of Me-(OCH2CH2)n—OH (n=1-11, 13) with X—(CH2)m—CO2R (X=Br or OMs) and subsequent hydrolysis led to PEG oligomer library III in 30-60% overall yields. Combinatorial purification techniques were adapted to the larger-scale library synthesis. A total of 498 compounds, each with a weight of 2-5 g and a minimum purity of 90%, were synthesized.

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