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17557-23-2

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17557-23-2 Usage

Chemical Properties

colourless liquid

Uses

Different sources of media describe the Uses of 17557-23-2 differently. You can refer to the following data:
1. Thismay be used as a bifunctional reactive diluent for viscosity reduction of resins with minimum change in cured resin properties and to allow increased filler incorporation.
2. Neopentyl Glycol Diglycidyl Ether is used in preparation of aqueous Epoxy curing agents for orange peel-like leveling coatings.
3. NGDE can be used in the synthesis of epoxy polymers for the development of shape memory polymers. It can also be used in the photopolymerization of cationic polymers.

Production Methods

The ether is made by condensing neopentyl glycol with epichlorohydrin followed by dehydrochlorination with caustic.

General Description

Clear liquid.

Air & Water Reactions

Slightly soluble in water.

Reactivity Profile

Neopentyl glycol diglycidyl ether is a ether-alcohol derivative. The ether being relatively unreactive. Flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents. They react with oxoacids and carboxylic acids to form esters plus water. Oxidizing agents convert alcohols to aldehydes or ketones. Alcohols exhibit both weak acid and weak base behavior. They may initiate the polymerization of isocyanates and epoxides.

Fire Hazard

Neopentyl glycol diglycidyl ether is combustible.

Carcinogenicity

A 2 year dermal carcinogenicity study of NPGDGE in C3H mice was conducted at dose levels of 0.94, 1.87, and 3.75 mg/mouse . Skin tumor incidences were 10/50, 6/50, and 0/50 at 3.75, 1.87, and 0.94 mg/ mouse; no tumors occurred in the 300 acetone-treated controls. Tumor potency was calculated to be 1/700th that of benzo[a]pyrene, which was tested concurrently.

Check Digit Verification of cas no

The CAS Registry Mumber 17557-23-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,5 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17557-23:
(7*1)+(6*7)+(5*5)+(4*5)+(3*7)+(2*2)+(1*3)=122
122 % 10 = 2
So 17557-23-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O3.C5H12O2/c1(5-3-8-5)7-2-6-4-9-6;1-5(2,3-6)4-7/h5-6H,1-4H2;6-7H,3-4H2,1-2H3

17557-23-2 Well-known Company Product Price

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  • (Code)Product description
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  • Aldrich

  • (338036)  Neopentylglycoldiglycidylether  technical grade

  • 17557-23-2

  • 338036-100ML

  • 563.94CNY

  • Detail
  • Aldrich

  • (338036)  Neopentylglycoldiglycidylether  technical grade

  • 17557-23-2

  • 338036-500ML

  • 2,197.26CNY

  • Detail

17557-23-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Neopentyl Glycol Diglycidyl Ether

1.2 Other means of identification

Product number -
Other names Diglycidyl Ether of Neo-Pentyl Glycol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Adhesives and sealant chemicals,CBI,Paint additives and coating additives not described by other categories
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:17557-23-2 SDS

17557-23-2Downstream Products

17557-23-2Relevant articles and documents

Nucleophilic opening of bis-epoxides: A new access to symmetrically functionalised macrocycles

Sebban, Mohamed Faouzi,Vottero, Philippe,Alagui, Abdelhakim,Dupuy, Claude

, p. 1019 - 1022 (2000)

A series of polyhydroxylated symmetrical macrocycles has been prepared in satisfactory yield by 1:1 condensation of several bis-epoxides with various bis-nucleophiles. Preliminary results are reported, which illustrate the synthesis of crown ethers and oxa-azacrown and oxa-thiacrown compounds. (C) 2000 Elsevier Science Ltd.

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