07-0055
Decahydronaphthalene, mixture of cis + trans
SAJ first grade, ≥98.0%
Synonim(y):
Decalin™
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Informacje o tej pozycji
Wzór empiryczny (zapis Hilla):
C10H18
Numer CAS:
Masa cząsteczkowa:
138.25
EC Number:
202-046-9
UNSPSC Code:
12352001
PubChem Substance ID:
Beilstein/REAXYS Number:
878165
MDL number:
Assay:
≥98.0%
Form:
liquid
Pomoc techniczna
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Pozwól nam pomócgrade
SAJ first grade
vapor density
4.76 (vs air)
vapor pressure
42 mmHg ( 92 °C), 741 mmHg ( 188 °C)
assay
≥98.0%
form
liquid
autoignition temp.
482 °F
expl. lim.
0.7-4.9 %, 100 °F
availability
available only in Japan
refractive index
n20/D 1.474 (lit.)
bp
189-191 °C (lit.)
mp
−125 °C (lit.)
density
0.896 g/mL at 25 °C (lit.)
SMILES string
C1CCC2CCCCC2C1
InChI
1S/C10H18/c1-2-6-10-8-4-3-7-9(10)5-1/h9-10H,1-8H2
InChI key
NNBZCPXTIHJBJL-UHFFFAOYSA-N
Legal Information
Decalin is a trademark of Sigma-Aldrich Co. LLC
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1C
Klasa składowania
3 - Flammable liquids
wgk
WGK 3
flash_point_f
134.6 °F - closed cup
flash_point_c
57 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
Lin Zhu et al.
Journal of natural products, 75(4), 567-571 (2012-03-08)
Five new decalin derivatives (1-5), together with two known compounds (6 and 7), were isolated from the ethyl acetate extract of red yeast rice. Their structures were elucidated by means of NMR and mass spectroscopic analyses. Monascusic lactone A (1)
Joseph B Lim et al.
The journal of physical chemistry. B, 116(1), 203-210 (2011-12-06)
A modification of the CHARMM36 lipid force field (C36) for cholesterol, henceforth, called C36c, is reported. A fused ring compound, decalin, was used to model the steroid section of cholesterol. For decalin, C36 inaccurately predicts the heat of vaporization (~10
Franco Cataldo et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 77(5), 998-1004 (2010-09-25)
Oleum (fuming sulphuric acid), a well known superacid, was used as medium for the generation of the radical cation of a series of selected PAHs. The resulting radical cation spectra were studied by electronic absorption spectroscopy. Not only common PAHs