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Key Documents

B7381

Sigma-Aldrich

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:
Pricing and availability is not currently available.

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

Product No.
Description
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Pictograms

CorrosionExclamation mark

Signal Word

Danger

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

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D S Pepper
Molecular biotechnology, 2(2), 157-178 (1994-10-01)
Three different coupling chemistries that have been tried and tested for use in affinity chromatography are described. These methods are particularly recommended for use by workers who do not have access to, or do not wish to use, complex organic
Petr Kubán et al.
Analytical chemistry, 79(14), 5462-5467 (2007-06-21)
The preparation and performance of a multilayered stationary phase for open tubular anion exchange chromatography in relatively large bore (75 microm diameter) columns are described. The inner surface of a fused-silica capillary tube is coated with up to 25 successive
A Nicoletti et al.
Journal of materials science. Materials in medicine, 24(1), 17-35 (2012-10-12)
Serious cartilage lesions (Outerbridge III, IV) may be successfully treated with a three-layered gradient scaffold made by magnesium-doped hydroxyapatite and type I collagen, manufactured through a bio-inspired process and stabilised by a reactive bis-epoxy (1,4-butanediol diglycidyl ether, BDDGE). Each layer
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

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