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88571

Sigma-Aldrich

1,6-Hexanediol solution

BioUltra, ~6 M in H2O

Synonym(s):

α,ω-Hexanediol, Hexamethylene glycol

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About This Item

CAS Number:
629-11-8
EC Number:
211-074-0
MDL number:
MFCD00002985
UNSPSC Code:
12352200
PubChem Substance ID:
57653317
NACRES:
NA.26

product line

BioUltra

form

liquid

concentration

~6 M in H2O

impurities

insoluble matter, passes filter test

cation traces

Al: ≤5 mg/kg
Ba: ≤5 mg/kg
Bi: ≤5 mg/kg
Ca: ≤10 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
K: ≤50 mg/kg
Li: ≤5 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Mo: ≤5 mg/kg
Na: ≤50 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Sr: ≤5 mg/kg
Zn: ≤5 mg/kg

λ

neat

UV absorption

λ: 260 nm Amax: 0.1
λ: 280 nm Amax: 0.1

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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Related Categories

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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
M A Rahman et al.
Dental materials journal, 14(2), 230-235 (1995-12-01)
The optimum concentration and application time for an experimental dentin primer composed of an aqueous solution of 1,6-hexanediol were determined by measuring the wall-to-wall polymerization contraction gap width of a commercial light-activated resin composite in a cylindrical dentin cavity prepared
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
Jennifer Tuma et al.
The journal of physical chemistry. B, 111(45), 13101-13106 (2007-10-26)
The solution structure of a synthetic DNA mini-hairpin possessing a stilbenediether linker and three G:C base pairs has been obtained using (1)H NMR spectral data and constrained torsion angle molecular dynamics. Notable features of this structure include a compact hairpin
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