52800
1,6-Hexanediol
purum, ≥95.0% (GC)
Synonym(s):
Hexamethylene glycol
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About This Item
Linear Formula:
HO(CH2)6OH
CAS Number:
Molecular Weight:
118.17
EC Number:
211-074-0
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
1633461
vapor pressure
0.53 mmHg ( 20 °C)
grade
purum
assay
≥95.0% (GC)
autoignition temp.
608 °F
expl. lim.
16 %
impurities
0.3-3% water
bp
250 °C (lit.)
mp
38-42 °C (lit.), 41-43 °C
solubility
H2O: 0.1 g/mL, clear, colorless
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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Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
215.6 °F - closed cup
flash_point_c
102 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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D Pandolfi et al.
Nucleosides & nucleotides, 18(9), 2051-2069 (1999-11-05)
Synthetic oligonucleotides are increasingly used because of their potential activity as regulators of gene expression. One of their major drawbacks is instability toward nucleases, in particular exonucleases. In this article, we studied some terminal modifications that can enhance exonuclease resistance
Nataliya Shulga et al.
Molecular and cellular biology, 23(2), 534-542 (2003-01-02)
The nuclear pore complex (NPC) is a permeable sieve that can dilate to facilitate the bidirectional translocation of a wide size range of receptor-cargo complexes. The binding of receptors to FG nucleoporin docking sites triggers channel gating by an unknown
M J Politis et al.
Journal of neurocytology, 9(4), 505-516 (1980-08-01)
This study examined the thesis that 2,5-dexanedione (2,5-HD) produces distal (dying-back) axonopathy by direct toxic action on nerve fibers. Single or repeated application of undiluted or 10% 2,5-HD to exposed rat sciatic nerves caused some fibres to develop focal axonal
R J Shamberger
Clinical chemistry, 33(4), 589-591 (1987-04-01)
In this assay for lactate dehydrogenase (EC 1.1.1.27) isoenzyme 1 (LD-1), 1,6-hexanediol is added to serum after total LD has been measured. After incubation for 5 min the total LD remaining is determined. Samples from patients who had a myocardial
M Durand et al.
Nucleic acids research, 18(21), 6353-6359 (1990-11-11)
An oligodeoxyribonucleotide, d(GCTCACAAT-X-ATTGTGAGC), where X represents a hexaethylene glycol chain, was studied using circular dichroism spectroscopy. Its conformation and conformational stability were compared to those of compounds where X was replaced by four thymines and to the duplex of same
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