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117606-92-5

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117606-92-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117606-92-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,6,0 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 117606-92:
(8*1)+(7*1)+(6*7)+(5*6)+(4*0)+(3*6)+(2*9)+(1*2)=125
125 % 10 = 5
So 117606-92-5 is a valid CAS Registry Number.

117606-92-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name cetyl glycidyl ether

1.2 Other means of identification

Product number -
Other names hexadecyl glycidyl 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:117606-92-5 SDS

117606-92-5Relevant articles and documents

Synthesis and thermotropic properties of novel double-chained quaternary ammonium chlorides with symmetric and asymmetric hydrocarbon chain length

Ding, Zhaoyun,Hao, Aiyou

, p. 127 - 131 (2009)

A series of novel double-chained quaternary ammonium chlorides with symmetrical and asymmetrical hydrocarbon chain length R1-O-CH2-CH(OH)-CH2-N+(CH3)2-R2·Cl- (R1, R2: C12H25, C14H29, C16H33) have been synthesized by the reaction of 1-O-alkyl glycidyl ether with N,N-dimethylalkylamine and N,N-dimethylalkylamine hydrochloride. Their chemical structures have been characterized through FT-IR, 1H NMR, MS and elementary analysis. Their thermotropic properties have been examined by differential scanning calorimetry (DSC), polarizing light microscopy (PLM) and X-ray diffraction (XRD). It has been found that the compounds with longer hydrocarbon chain length and being higher asymmetry in hydrocarbon chain length exhibit lower melting point (Tm), isotropization temperature (Ti) and narrower mesophase temperature range. However, the hydrocarbon chain length and the symmetry in the hydrocarbon chain length have little influence on the type of liquid crystals. All compounds form cholesteric liquid crystal.

Physicochemical properties of novel phosphobetaine zwitterionic surfactants and mixed systems with an anionic surfactant

Nong, Lanping,Xiao, Chengliang,Zhong, Zhensheng

, p. 433 - 438 (2011)

A series of novel zwitterionic phosphobetaine (PPBT) surfactants were synthesized using long chain fatty alcohol, epichlorohydrin, dimethylamine and sodium dihydrogen phosphate as raw materials. The physicochemical properties of the phosphobetaine surfactants such as isoelectric point, foaming, surface tension, critical micelle concentration (CMC) and Krafft point were measured. Low CMC and surface tension values indicated the surface activities of the phosphobetaine surfactants were quite excellent. The CMC and surface tension values of PPBT/SDS mixed systems were determined. It was found both of CMC and surface tension values decreased compared with single surfactant system because of the association between dodecyl sulfate anions and cationic groups in phosphobetaine by electrostatic attraction. AOCS 2011.

Synthesis, Surface and Antimicrobial Activities of Novel Cationic Gemini Surfactants

Ding, Zhaoyun,Fang, Shimin

, p. 1051 - 1057 (2015)

A series of novel cationic gemini surfactants [C n H2n+1-O-CH2-CH(OH)-CH2-N+(CH3)2-(CH2)2]2·2Br- [3a (n = 12), 3b (n = 14) and 3c (n = 16)] having a 2-hydroxy-1,3-oxypropylene group [-CH2-CH(OH)-CH2-O-] in the hydrophobic chain have been synthesized and characterized. Their water solubility, surface activity, foaming properties, and antibacterial activity have been examined. The critical micelle concentration (CMC) values of the novel cationic gemini surfactants are one to two orders of magnitude smaller than those of the corresponding monomeric surfactants. Furthermore, the novel cationic gemini surfactants have better water solubility and surface activity than the comparable [C n H2n+1-N+(CH3)2-(CH2)2]2·2Br- (n-4-n) geminis. The novel cationic gemini surfactants 3a and 3b also exhibit good foaming properties and show good antibacterial and antifungal activities.

Synthesis of natural 1- O -alkylglycerols: A study on the chemoselective opening of the epoxide ring by onium quaternary salts (N and P) and ionic liquids

Nascimento, Thiana Santiago,Braga, Esther Faria,Casaes Gomes, Giselle Cristina,Batista, William Rom?o,Mazzei Albert, André Luís,Capella Lopes, Rosangela Sabbatini,Lopes, Claudio Cerqueira

, p. 1050 - 1054 (2020/01/23)

A chemoselective route for the synthesis of 1-O-alkylglycerols chimyl (1), batyl (2), and selachyl (3) is reported. These compounds can be naturally isolated from shark liver oil and the skin of animals such as stingrays and chimeras and exhibit potential anti-fouling activity. The synthetic approach developed in this work included two distinct methods of preparation. The first was based on solvent-free reactions catalyzed by onium quaternary salts (N and P) and ionic liquids; the second methodology was based on a series of one-pot reactions.

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