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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存储类别
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)
法规信息
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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
Roosmarijn E Vandenbroucke et al.
The journal of gene medicine, 10(7), 783-794 (2008-05-13)
Small interfering (si)RNA mediated inhibition of oncogenes or viral genes may offer great opportunities for the treatment of several diseases such as hepatocellular carcinoma and viral hepatitis. However, the development of siRNAs as therapeutic agents strongly depends on the availability
K Tanishima et al.
Clinical chemistry, 31(7), 1175-1177 (1985-07-01)
To measure activities of lactate dehydrogenase (EC 1.1.1.27) isoenzymes LD1 and LD2 in serum, we developed a method involving 1,6-hexanediol as specific inhibitor of the M-subunit. Addition of hexanediol, 0.6 mol/L, to five LD isoenzyme fractions purified from human liver
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
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