4016-11-9 Usage
Description
ETHYL GLYCIDYL ETHER is a colorless, highly flammable, and polymerizable liquid with a flash point near 100°F. It is less dense than water and can cause severe irritation to the skin, eyes, and mucous membranes. Ingestion, inhalation, and skin absorption may also result in toxicity.
Uses
Used in Chemical Synthesis:
ETHYL GLYCIDYL ETHER is used as a chemical intermediate for the synthesis of various compounds, such as glycidyl ethers and epoxides, due to its reactive epoxy and ethyl groups.
Used in Pharmaceutical Industry:
ETHYL GLYCIDYL ETHER is used as a starting material for the production of pharmaceutical compounds, as its chemical properties allow for the creation of diverse drug molecules with potential therapeutic applications.
Used in Coatings and Adhesives:
ETHYL GLYCIDYL ETHER is used as a reactive diluent in the coatings and adhesives industry, where its ability to polymerize helps improve the performance and properties of the final products.
Used in Composite Materials:
ETHYL GLYCIDYL ETHER is used as a component in the manufacturing of composite materials, where its polymerization properties contribute to the formation of strong and durable materials.
Used in Surface Treatments:
ETHYL GLYCIDYL ETHER is used in surface treatments, such as adhesion promoters and coupling agents, to enhance the bonding between different materials, like plastics, metals, and ceramics.
Used in Electronic Industry:
ETHYL GLYCIDYL ETHER is used in the electronic industry as a component in the production of encapsulants and potting compounds, which protect electronic components from environmental factors and mechanical stress.
Air & Water Reactions
Highly flammable. Soluble with possible partial decomposition in water.
Reactivity Profile
An epoxide and ether. Ethers 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. Epoxides are highly reactive. They polymerize in the presence of catalysts or when heated. These polymerization reactions can be violent. Compounds in this group react with acids, bases, and oxidizing and reducing agents. They react, possibly violently with water in the presence of acid and other catalysts.
Health Hazard
Inhalation or contact with material may irritate or burn skin and eyes. Fire may produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control may cause pollution.
Fire Hazard
HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.
Safety Profile
Mutation data reported.
A flammable liquid. When heated to
decomposition it emits acrid smoke and
irritating vapors.
Potential Exposure
It has limited commercial use in
organic synthesis.
Shipping
UN2752 1,2-Epoxy-3-ethoxypropane, Hazard
Class: 3; Labels: 3-Flammable liquid
Incompatibilities
Polymerizable. Keep away from strong
oxidizers, heat, flames
Waste Disposal
Dissolve or mix the material
with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal,
state, and local environmental regulations must be
observed.
Check Digit Verification of cas no
The CAS Registry Mumber 4016-11-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,1 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4016-11:
(6*4)+(5*0)+(4*1)+(3*6)+(2*1)+(1*1)=49
49 % 10 = 9
So 4016-11-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H10O2/c1-2-6-3-5-4-7-5/h5H,2-4H2,1H3/t5-/m1/s1
4016-11-9Relevant articles and documents
Rational design 2-hydroxypropylphosphonium salts as cancer cell mitochondria-targeted vectors: Synthesis, structure, and biological properties
Amerhanova, Syumbelya K.,Dimukhametov, Mudaris N.,Gubaidullin, Aidar T.,Islamov, Daut R.,Litvinov, Igor A.,Lyubina, Anna P.,Mironov, Vladimir F.,Nemtarev, Andrey V.,Pashirova, Tatiana N.,Titov, Eugenii A.,Tsepaeva, Olga V.,Voloshina, Alexandra D.
, (2021/11/01)
It has been shown for a wide range of epoxy compounds that their interaction with triphenylphosphonium triflate occurs with a high chemoselectivity and leads to the formation of (2-hydroxypropyl)triphenylphosphonium triflates 3 substituted in the 3-position with an alkoxy, alkylcarboxyl group, or halogen, which were isolated in a high yield. Using the methodology for the disclosure of epichlorohydrin with alcohols in the presence of boron trifluoride ether-ate, followed by the substitution of iodine for chlorine and treatment with triphenylphosphine, 2-hydroxypropyltriphenylphosphonium iodides 4 were also obtained. The molecular and supramolec-ular structure of the obtained phosphonium salts was established, and their high antitumor activity was revealed in relation to duodenal adenocarcinoma. The formation of liposomal systems based on phosphonium salt 3 and L-α-phosphatidylcholine (PC) was employed for improving the bioavailabil-ity and reducing the toxicity. They were produced by the thin film rehydration method and exhibited cytotoxic properties. This rational design of phosphonium salts 3 and 4 has promising potential of new vectors for targeted delivery into mitochondria of tumor cells.
hybrid-fluorinated non-ionic surfactant with short perfluoroalkyl chains and preparation method thereof
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Paragraph 0178-0181; 0189-0192, (2018/07/03)
The present invention relates to a hybrid fluorine-based nonionic surfactant containing a short fluorinated alkyl group, and a preparing method thereof, and more particularly, to a hybrid fluorine-based nonionic surfactant having one low fluorinated alkyl group and one hydrocarbon group, and a preparing method thereof. According to the present invention, the hybrid fluorine-based nonionic surfactant realizes a low surface tension and CMC even though a short fluorinated alkyl group is included in one molecule, and has high solubility in water and excellent emulsification stability, and thus has excellent physical properties as a surfactant. In addition, the hybrid fluorine-based nonionic surfactant is less harmful to the human body and the environment compared to a conventional surfactant due to low fluorinated alkyl group, and requires low manufacturing costs and thus can be beneficially used as an eco-friendly and economical fluorine-based nonionic surfactant having competitiveness in terms of price. In particular, the hybrid fluorine-based nonionic surfactant of the present invention can be beneficially used as a surfactant replacing a conventional fluorine-based nonionic surfactant containing a long perfluorinated alkyl group such as PFOA or PFOS known to be harmful to the environment and the human body.COPYRIGHT KIPO 2018
SYNTHESIS AND UTEROSTIMULATING ACTIVITY OF DERIVATIVES OF 1-DIALKYLAMINO-3-ALKOXY-2-PROPANOL
Zaitsev, L. M.,Korotkii, Yu. V.,Krasavtsev, I. I.,Lozinskii, M. O.
, p. 492 - 495 (2007/10/02)
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