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H11807

Sigma-Aldrich

1,6-Hexanediol

97%

Synonym(s):

Hexamethylene glycol

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About This Item

Linear Formula:
HO(CH2)6OH
CAS Number:
Molecular Weight:
118.17
Beilstein/REAXYS Number:
1633461
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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

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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

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

215.6 °F - closed cup

flash_point_c

102 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)


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’.

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Clinton Belott et al.
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
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Ince, Mine et al.
Journal of Materials Chemistry, 21(5), 1531-1536 (2011)
A series of furan-aromatic polyesters synthesized via direct esterification method based on renewable resources.
Jiang, Min et al.
Journal of Polymer Science Part A: Polymer Chemistry, 50(5), 1026-1036 (2012)
Melt-phase synthesis and properties of triptycene-containing copolyesters.
Liu, Yanchun et al.
Macromolecules, 44(11), 4049-4056 (2011)

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