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C14E8 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 27847-86-5 Structure
  • Basic information

    1. Product Name: C14E8
    2. Synonyms: OCTAETHYLENE GLYCOL MONOTETRADECYL ETHER;POLYOXYETHYLENE 8 MYRISTYL ETHER;TETRADECYL OCTAETHYLENE GLYCOL ETHER;TETRADECYLOCTAGLYCOL;C14E8;3,6,9,12,15,18,21,24-Octaoxaoctatriacontan-1-ol;C14E8, Polyoxyethylene (8) myristyl ether, Tetradecyl octaethylene glycol ether, Tetradecyloctaglycol
    3. CAS NO:27847-86-5
    4. Molecular Formula: C30H62O9
    5. Molecular Weight: 566.81
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 27847-86-5.mol
  • Chemical Properties

    1. Melting Point: 38-39 °C
    2. Boiling Point: 607.3°C at 760 mmHg
    3. Flash Point: 321.1°C
    4. Appearance: colourless solid
    5. Density: 0.99g/cm3
    6. Vapor Pressure: 2.78E-17mmHg at 25°C
    7. Refractive Index: 1.459
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. Stability: Stable. Incompatible with strong oxidizing agents.
    11. CAS DataBase Reference: C14E8(CAS DataBase Reference)
    12. NIST Chemistry Reference: C14E8(27847-86-5)
    13. EPA Substance Registry System: C14E8(27847-86-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: 24/25
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 27847-86-5(Hazardous Substances Data)

27847-86-5 Usage

Chemical Properties

colourless solid

Check Digit Verification of cas no

The CAS Registry Mumber 27847-86-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,8,4 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 27847-86:
(7*2)+(6*7)+(5*8)+(4*4)+(3*7)+(2*8)+(1*6)=155
155 % 10 = 5
So 27847-86-5 is a valid CAS Registry Number.
InChI:InChI=1/C30H62O9/c1-2-3-4-5-6-7-8-9-10-11-12-13-15-32-17-19-34-21-23-36-25-27-38-29-30-39-28-26-37-24-22-35-20-18-33-16-14-31/h31H,2-30H2,1H3

27847-86-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names Tetradecyl octaethylene glycol ether

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:27847-86-5 SDS

27847-86-5Upstream product

27847-86-5Downstream Products

27847-86-5Relevant articles and documents

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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