B7381
1,4-Butanediyl diglycidyl ether
~70%
Synonym(s):
Araldite® RD-2
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About This Item
Empirical Formula (Hill Notation):
C10H18O4
CAS Number:
Molecular Weight:
202.25
Beilstein:
115238
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
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Assay
~70%
bp
155-160 °C/11 mmHg
density
1.05 g/mL (lit.)
SMILES string
C(CCOCC1CO1)COCC2CO2
InChI
1S/C10H18O4/c1(3-11-5-9-7-13-9)2-4-12-6-10-8-14-10/h9-10H,1-8H2
InChI key
SHKUUQIDMUMQQK-UHFFFAOYSA-N
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Legal Information
Araldite is a registered trademark of Huntsman Advanced Materials Inc.
replaced by
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Description
Pricing
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1
Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Flash Point(F)
235.4 °F - closed cup
Flash Point(C)
113 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Cesar G Gomez et al.
Journal of biochemical and biophysical methods, 55(1), 23-36 (2003-02-01)
The influence of the morphology of ethylene glycol dimethacrylate-hydroxyethyl methacrylate copolymer [poly(EGDMA-co-HEMA)] base support to obtain different Fe(3+)-containing sorbents and their properties in retention of O-phosphothreonine [Thre(P)] is examined in this paper. Three base supports poly(EGDMA-co-HEMA) (I-III) were obtained using
M P Markowicz et al.
The International journal of artificial organs, 29(12), 1167-1173 (2007-01-16)
Ongoing research has achieved much progress towards the development of new artificial skin substitute products. However, effective implant material for correcting full-thickness defects (such as those arising from extensive burns, tumor resection, hereditary or congenital defects and chronic wounds) has
Anabela Alves et al.
International journal of pharmaceutics, 426(1-2), 76-81 (2012-01-28)
The polysaccharide ulvan, composed of sulphated rhamnose, glucoronic and iduronic acids was used to produce polymeric membranes by solvent casting. As ulvan is soluble in water, a cross-linking step was necessary to render the membrane insoluble in water and stable
R Zeeman et al.
Journal of biomedical materials research, 46(3), 424-433 (1999-07-09)
Crosslinking of dermal sheep collagen (DSC) was accomplished using 1, 4-butanediol diglycidyl ether (BDDGE). At pH values > 8.0, epoxide groups of BDDGE will react with amine groups of collagen. The effects of BDDGE concentration, pH, time, and temperature were
Laura Oakey et al.
Analytical biochemistry, 335(2), 316-325 (2004-11-24)
This study reevaluates the potential for direct coupling of NAD(P)(+) to a carboxylate-terminating spacer arm using carbodiimide-promoted coupling in an attempt to develop a greatly simplified synthetic method for cofactor immobilization that would support the more widespread adoption of kinetic-based
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