TRIETHYLENE GLYCOL MONOMETHYL ETHER (TM)

Basic information

  • Product Name:TRIETHYLENE GLYCOL MONOMETHYL ETHER (TM)
  • CasNo.:112-35-6
  • MF:C7H16O4
  • MW:164.202

Physical and Chemical Properties

  • Purity:99%
  • Boiling Point:-44oC
  • Packing:Colorless odorless liquid
  • Throughput:
Inquiry

Product Details

CasNo: 112-35-6

MF: C7H16O4

Appearance: Colorless odorless liquid

Factory supply TRIETHYLENE GLYCOL MONOMETHYL ETHER (TM) 112-35-6 with sufficient production capacity

  • Molecular Formula:C7H16O4
  • Molecular Weight:164.202
  • Appearance/Colour:Colorless odorless liquid 
  • Vapor Pressure:<0.01 mm Hg ( 20 °C) 
  • Melting Point:-44oC 
  • Refractive Index:n20/D 1.439(lit.)  
  • Boiling Point:233.9 °C at 760 mmHg 
  • PKA:14.36±0.10(Predicted) 
  • Flash Point:95.3 °C 
  • PSA:47.92000 
  • Density:1.021 g/cm3 
  • LogP:-0.34170 

TRIETHYLENE GLYCOL MONOMETHYL ETHER(Cas 112-35-6) Usage

Air & Water Reactions

Ethers tend to form unstable peroxides when exposed to oxygen. Ethyl, isobutyl, ethyl tert-butyl, and ethyl tert-pentyl ether are particularly hazardous in this respect. Ether peroxides can sometimes be observed as clear crystals deposited on containers or along the surface of the liquid.

Reactivity Profile

Ethers, such as TRIETHYLENE GLYCOL MONOMETHYL ETHER, can act as bases. They form salts with strong acids and addition complexes with Lewis acids. The complex between diethyl ether and boron trifluoride is an example. Ethers may react violently with strong oxidizing agents. In other reactions, which typically involve the breaking of the carbon-oxygen bond, ethers are relatively inert.

Health Hazard

No appreciable hazard in ordinary handling or use.

Safety Profile

Mildly toxic by ingestion and skincontact. A skin and eye irritant. Many glycol ethercompounds have dangerous human reproductive effects.Combustible when exposed to heat or flame. To fight fire,use alcohol foam, dry chemical. When heated todecomposit

Definition

ChEBI: A hydroxypolyether that is the monomethyl ether derivative of triethylene glycol. Metabolite observed in cancer metabolism.

General Description

Colorless odorless liquid.

InChI:InChI=1/C7H16O4/c1-9-4-5-11-7-6-10-3-2-8/h8H,2-7H2,1H3

112-35-6 Relevant articles

Squaraine-derived rotaxanes: Highly stable, fluorescent near-IR dyes

Arunkumar, Easwaran,Fu, Na,Smith, Bradley D.

, p. 4684 - 4690 (2006)

Squaraines are fluorescent, near-IR dyes...

Synthesis of glycol ethers and their use for intensification of oil recovery

Lebedeva,Mazaev,Tret'yakov

, p. 1415 - 1417 (2001)

Monoalkyl ethers of ethylene and triethy...

-

Takahashi,H.,Kuwamura,T.

, p. 623 - 626 (1973)

-

Effect of carboxylic acid on micelles of a neutral amphiphilic dendro-calix[4]arene

Huang, Hong,Li, Dong-Mi,Wang, Weizhou,Chen, Yi-Chang,Khan, Khalid,Song, Song,Zheng, Yan-Song

, p. 729 - 735 (2012)

An amphiphilic calix[4]arene bearing bra...

Synthesis, characterization and spectroscopic properties of water soluble coumarins substituted with oligomeric alkoxy functions

Surya Prakash Rao,Babu, Mohan,Desai, Avinash

, p. 11064 - 11072 (2014)

Novel water soluble robust fluorescent c...

Inclusion complexes of a new family of non-ionic amphiphilic dendrocalix[4]arene and poorly water-soluble drugs naproxen and ibuprofen

Khan, Khalid,Lal Badshah, Syed,Ahmad, Nasir,Rashid, Haroon Ur,Mabkhot, Yahia

supporting information, (2017/06/08)

The inclusion complexes of a new family ...

Bis-TEGylated poly(p-benzamide)s: Combining organosolubility with shape persistence

Schulze, Maren,Michen, Benjamin,Fink, Alke,Kilbinger, Andreas F. M.

, p. 5520 - 5530 (2013/08/23)

The synthesis of perfectly planar, bis-s...

112-35-6 Process route

3-Hydroxybenzyl alcohol
620-24-6

3-Hydroxybenzyl alcohol

triethylene glucol monomethyl ether
112-35-6,95507-80-5

triethylene glucol monomethyl ether

3-Phenoxybenzyl alcohol
13826-35-2

3-Phenoxybenzyl alcohol

Conditions
Conditions Yield
87%
dimethyl sulfate
77-78-1

dimethyl sulfate

2,2'-[1,2-ethanediylbis(oxy)]bisethanol
112-27-6

2,2'-[1,2-ethanediylbis(oxy)]bisethanol

triethylene glucol monomethyl ether
112-35-6,95507-80-5

triethylene glucol monomethyl ether

Conditions
Conditions Yield
With sodium hydroxide; at 120 ℃; for 4h;
59%
With sodium hydroxide; at 120 ℃;

112-35-6 Upstream products

  • 75-21-8
    75-21-8

    oxirane

  • 67-56-1
    67-56-1

    methanol

  • 109-86-4
    109-86-4

    2-methoxy-ethanol

  • 249508-40-5
    249508-40-5

    triethylene glycol benzyl methyl ether

112-35-6 Downstream products

  • 52995-76-3
    52995-76-3

    1-chloro-3,6,9-trioxadecane

  • 23601-40-3
    23601-40-3

    hexaethylene glycol monomethyl ether

  • 1072-40-8
    1072-40-8

    2,5,8,11,14,17,20-heptaoxahenicosane

  • 65633-96-7
    65633-96-7

    2-[4-(2,4-Dichloro-phenoxy)-phenoxy]-propionic acid 2-[2-(2-methoxy-ethoxy)-ethoxy]-ethyl ester