Skip to Content
Merck
All Photos(1)

Documents

371130

Sigma-Aldrich

1,4-Diisocyanatobutane

97.0%

Synonym(s):

Tetramethylene diisocyanate

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
OCN(CH2)4NCO
CAS Number:
Molecular Weight:
140.14
Beilstein:
1756894
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

Assay

97.0%

form

liquid

bp

102-104 °C/14 mmHg (lit.)

density

1.105 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

O=C=NCCCCN=C=O

InChI

1S/C6H8N2O2/c9-5-7-3-1-2-4-8-6-10/h1-4H2

InChI key

OVBFMUAFNIIQAL-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

1,4-Diisocyanatobutane is a highly reactive compound with two isocyanate (-NCO) groups separated by a butane chain. It can undergo reactions such as urethane formation, crosslinking, and chain extension. It is widely used as a building block to synthesize polyurethane-based materials with excellent flexibility, impact resistance, and mechanical properties, making them useful in tissue engineering, contact lenses, biocompatible coatings, adhesives, foams, elastomers, and sealants.

Application

1,4-Diisocyanatobutanecan be used in the following fields:

Tissue engineering -As a precursor to synthesize polyurethane composites which can be used as 3D scaffolds for tissue engineering,

Contact lenses- As a cross-linking agent to prepare inorganic-organic hydrogel contact lenses for high refractive index ocular refractive correction biomaterial,

Controlled drug delivery- As a chain extender to synthesize segmented polyurethanes for redox-sensitive controlled drug release systems.

Pictograms

Health hazardExclamation mark

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

222.8 °F - closed cup

Flash Point(C)

106 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Synthesis and characterization of redox-sensitive polyurethanes based on l-glutathione oxidized and poly(ether ester) triblock copolymers
Fabio S. Palumbo, et al.
Reactive and Functional Polymers, 126, 104986-104986 (2021)
Polymerizable-group capped ZnS nanoparticle for high refractive index inorganic-organic hydrogel contact lens
Peili Zhao, et al.
Materials Science and Engineering, C, 90, 485-493 (2018)
3D-composite scaffolds from radiation-induced chitosan grafted poly(3-hydroxybutyrate) polyurethane
Maykel Gonzalez Torres
Materials Today Communications, 23, 100902-100902 (2020)
Vladimir Burmistrov et al.
Bioorganic & medicinal chemistry letters, 24(9), 2193-2197 (2014-04-02)
A series of inhibitors of the soluble epoxide hydrolase (sEH) containing two urea groups has been developed. Inhibition potency of the described compounds ranges from 2.0 μM to 0.4 nM. 1,6-(Hexamethylene)bis[(adamant-1-yl)urea] (3b) was found to be a potent slow tight

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service