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25961-89-1

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25961-89-1 Usage

Uses

Different sources of media describe the Uses of 25961-89-1 differently. You can refer to the following data:
1. Agricultural chemical.
2. n-Hexyltrioxyethylene is a commercial repellent against Xenopsylla cheopis.

Hazard

A poison by ingestion.

Check Digit Verification of cas no

The CAS Registry Mumber 25961-89-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,9,6 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 25961-89:
(7*2)+(6*5)+(5*9)+(4*6)+(3*1)+(2*8)+(1*9)=141
141 % 10 = 1
So 25961-89-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H26O4/c1-2-3-4-5-7-14-9-11-16-12-10-15-8-6-13/h13H,2-12H2,1H3

25961-89-1SDS

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-hexoxyethoxy)ethoxy]ethanol

1.2 Other means of identification

Product number -
Other names C6E3

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Solvents (which become part of product formulation or mixture)
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:25961-89-1 SDS

25961-89-1Downstream Products

25961-89-1Relevant articles and documents

Tuning the lifetime of transient phases of mechanochromic gold isocyanide complexes through functionalization of the terminal moieties of flexible side chains

Seki, Tomohiro,Kashiyama, Kentaro,Yagai, Shiki,Ito, Hajime

, p. 1415 - 1418 (2017)

The lifetime of the transient phases of luminescent mechanochromic gold isocyanide complexes could be tuned through the modification of the termini of flexible side chains. Upon grinding, these complexes initially showed an emission color change from blue to yellow. The yellow emission spontaneously changed to blue or green, but with different lifetimes of the yellow-emitting transient phases depending on the substituents. Details of the mechano-induced structure changes were also described.

Self-assembling properties of non-ionic tetraphenylporphyrins and discotic phthalocyanines carrying oligo(ethylene oxide) alkyl or alkoxy units

Kroon, Johannes M.,Koehorst, Robert B. M.,Van Dijk, Marinus,Sanders, Georgine M.,Sudhoelter, Ernst J. R.

, p. 615 - 624 (2007/10/03)

The thermotropic phase behaviour and self-assembling features of some non-ionic tetraphenylporphyrins and phthalocyanines containing oligo(ethylene oxide) alkoxy or alkyl units have been investigated. From DSC measurements and polarization microscopy it was concluded that none of the tetraphenylporphyrins was mesomorphic while the phthalocyanines displayed discotic hexagonal phases even at room temperature. The aggregation of the compounds in aqueous media was studied by means of UV-VIS and fluorescence spectroscopy and it has been found that in water the tetraphenylporphyrins form J- or head-to-tail type of aggregates while phthalocyanines form H- or face-to-face type of aggregates. The luminescence properties of the tetraphenylporphyrin and phthalocyanine aggregates are explained on the basis of the molecular exciton approximation. Steric constraints and orientational disorder in the tetraphenylporphyrin aggregates determine the luminescence yield relative to the monomeric species. The cofacial arrangement of the macrocycles in phthalocyanine aggregates results in a forbidden S1-S0 transition and thus in a complete disappearance of the luminescence.

Topical mosquito repellents VII: Alkyl triethylene glycol monoethers

Johnson,DeGraw,Engstrom,Skinner,Brown,Skidmore,Maibach

, p. 693 - 695 (2007/10/05)

Normal and branched chain aliphatic monoethers of triethylene glycol are effective topical mosquito repellents. In terms of duration of protection, they are generally superior to the corresponding diethylene glycol analogs, and some are superior to diethyltoluamide. The n heptyl monoether of triethylene glycol affords double the protection time of diethyltoluamide under controlled laboratory conditions, and appears to be a useful new mosquito repellent.

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