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1,4-Butanediol Diglycidyl Ether

Product Introduction

1,4-Butanediol diglycidyl ether Basic information

Product Name:	1,4-Butanediol diglycidyl ether
Synonyms:	1,4-Butanediol diglycidyl ether >=95%;1,4-Butanediol diglycidyl ether technical grade, 60%;1,4-Butanediol diglycidyl ether, 98%, 98%;1,4-butandedioldiglycidylether;1,4-Butane diglycidyl ether;1,4-butanediglycidylether;1,4-Diglycidloxybutane;2-([4-(2-Oxiranylmethoxy)butoxy]methyl)oxirane
CAS:	2425-79-8
MF:	C10H18O4
MW:	202.25
EINECS:	219-371-7
Product Categories:	Epoxy Diluents;Epoxide Monomers;Oxiranes;Simple 3-Membered Ring Compounds;Monomers;Polymer Science;bc0001;2425-79-8
Mol File:	2425-79-8.mol

1,4-Butanediol diglycidyl ether Chemical Properties

Melting point	-21 °C
Boiling point	266 °C (lit.)
density	1.1 g/mL at 25 °C (lit.)
vapor pressure	~10 mm Hg ( 20 °C)
refractive index	n20/D 1.453
Fp	>230 °F
storage temp.	Inert atmosphere,2-8°C
solubility	Chloroform (Soluble), Methanol (Slightly)
form	Liquid
Specific Gravity	1.07
color	Clear yellow
Water Solubility	SOLUBLE
Sensitive	Hygroscopic
BRN	115238
Stability:	Hygroscopic
InChIKey	SHKUUQIDMUMQQK-UHFFFAOYSA-N
LogP	-0.27 at 25℃
CAS DataBase Reference	2425-79-8(CAS DataBase Reference)
NIST Chemistry Reference	Oxirane, 2,2'-[1,4-butanediylbis(oxymethylene)]bis-(2425-79-8)
EPA Substance Registry System	1,4-Butanediol diglycidyl ether (2425-79-8)

Hazard Codes	Xn
Risk Statements	20/21-36/38-43-52/53-22
Safety Statements	26-28-37/39-28B
WGK Germany	1
RTECS	EJ5100000
F	3-10
TSCA	Yes
HS Code	29109000
Hazardous Substances Data	2425-79-8(Hazardous Substances Data)
Toxicity	LD50 oral in rat: 1134mg/kg

MSDS Information

Provider	Language
1,4-Butanediol diglycidyl ether	English
ACROS	English
SigmaAldrich	English
ALFA	English

1,4-Butanediol diglycidyl ether Usage And Synthesis

Description	1,4-Butanediol diglycidyl ether is a reactive diluent in epoxy resins.
Chemical Properties	Clear yellow liquid
Uses
Uses	1,4-Butanediol diglycidyl ether is used for preparing amylose, xylan and hydroxyethyl-cellulose, to cross link polyethylenimine which also serves as a hole-blocking layer in organic solar cells, to cross link hyaluronic acid into hydrogels and for the activation of soluble dextran polymers. It is the most commonly used homobifunctional epoxide compound
Production Methods	The compound results from condensation of butanediol with epichlorohydrin followed by dehydrochlorination with caustic.
General Description	Clear pale yellow liquid.
Air & Water Reactions	Hygroscopic. Water soluble
Reactivity Profile	1,4-Butanediol diglycidyl ether reacts with acids.
Fire Hazard	1,4-Butanediol diglycidyl ether is combustible.
Flammability and Explosibility	Non flammable
Contact allergens	This substance is a reactive diluent in epoxy resins
Carcinogenicity	A2 year dermal cancer bioassay was conducted in CF1 mice at doses of 0%, 0.05%, and 0.2% in acetone . Treatment did not adversely affect survival, did not increase the incidence of skin tumors, and did not result in significant skin irritation. There were no statistically significant increases in incidence of any systemic tumors, except for lymphatic tumors in females. Because there was a high background incidence of this tumor type in CF1 mice used in the testing laboratory , there was no clear evidence of 1,4-BDDGE-induced carcinogenicity.