H11807
1,6-Hexanediol
97%
Synonym(s):
Hexamethylene glycol
Sign Into View Organizational & Contract Pricing
All Photos(4)
About This Item
Recommended Products
vapor pressure
0.53 mmHg ( 20 °C)
Assay
97%
autoignition temp.
608 °F
expl. lim.
16 %
bp
250 °C (lit.)
mp
38-42 °C (lit.)
SMILES string
OCCCCCCO
InChI
1S/C6H14O2/c7-5-3-1-2-4-6-8/h7-8H,1-6H2
InChI key
XXMIOPMDWAUFGU-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
Related Categories
Application
1,6-Hexanediol is generally used to introduce C6-spacer in molecular substrates. It is also widely used in the synthesis of various polyesters.
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
215.6 °F - closed cup
Flash Point(C)
102 °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.
Customers Also Viewed
Proceedings of the National Academy of Sciences of the United States of America, 117(44), 27676-27684 (2020-10-21)
Proteinaceous liquid-liquid phase separation (LLPS) occurs when a polypeptide coalesces into a dense phase to form a liquid droplet (i.e., condensate) in aqueous solution. In vivo, functional protein-based condensates are often referred to as membraneless organelles (MLOs), which have roles
Polymers, 12(9) (2020-08-28)
Among the various catalysts that can be used for polycondensation reactions, enzymes have been gaining interest for three decades, offering a green and eco-friendly platform towards the sustainable design of renewable polyesters. However, limitations imposed by their delicate nature, render
Liquid crystalline phthalocyanine-fullerene dyads.
Journal of Materials Chemistry, 21(5), 1531-1536 (2011)
A series of furan-aromatic polyesters synthesized via direct esterification method based on renewable resources.
Journal of Polymer Science Part A: Polymer Chemistry, 50(5), 1026-1036 (2012)
Melt-phase synthesis and properties of triptycene-containing copolyesters.
Macromolecules, 44(11), 4049-4056 (2011)
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