T19607
1,2,4,5-Tetramethylbenzene
98%
Synonym(s):
Durene, 1,2,4,5-Tetramethylbenzene
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All Photos(3)
About This Item
Linear Formula:
C6H2(CH3)4
CAS Number:
Molecular Weight:
134.22
Beilstein:
1903393
EC Number:
MDL number:
UNSPSC Code:
12352100
eCl@ss:
39011404
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
vapor density
4.6 (vs air)
Quality Level
vapor pressure
160 mmHg ( 140 °C)
Assay
98%
mp
76-80 °C (lit.)
density
0.838 g/mL at 25 °C (lit.)
SMILES string
Cc1cc(C)c(C)cc1C
InChI
1S/C10H14/c1-7-5-9(3)10(4)6-8(7)2/h5-6H,1-4H3
InChI key
SQNZJJAZBFDUTD-UHFFFAOYSA-N
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Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Flam. Sol. 1
Storage Class Code
4.1B - Flammable solid hazardous materials
WGK
WGK 1
Flash Point(F)
165.2 °F - closed cup
Flash Point(C)
74 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Joaquín Ortego et al.
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D Reichert et al.
Solid state nuclear magnetic resonance, 13(3), 137-148 (1999-02-19)
One- (1-D) and two-dimensional (2-D) carbon-13 NMR exchange measurements in powder samples of isotopically normal durene under magic angle spinning (MAS) are reported. The experiments include rotor synchronized 2-D exchange (RS2DE), 1-D magnetization transfer (MT) and time reverse ODESSA (tr-ODESSA).
Elin Rönnberg et al.
Immunology, 143(2), 155-163 (2014-04-03)
Staphylococcus aureus is a major pathogen that can cause a broad spectrum of serious infections including skin infections, pneumonia and sepsis. Peritoneal mast cells have been implicated in the host response towards various bacterial insults and to provide mechanistic insight
S David et al.
Journal of inorganic biochemistry, 28(2-3), 125-135 (1986-10-01)
Solution equilibria are presented for in situ reactions of the type FeII(porp) + B----FeII(porp)B, where porp represents the dianion of some durene-capped porphyrins with variable length linking methylene straps, and B is 1-methyl, 1,2-dimethyl, or 1,5-dicyclohexylimidazole. Increasing distortion of the
B C Gerstein et al.
Solid state nuclear magnetic resonance, 6(1), 63-71 (1996-02-01)
Delayed acquisition of the proton NMR in selected organic molecular solids (L-alanine, durene, ethyl fumarate, and p-hydroxybenzoic acid) is shown to allow the observation of mobile species in the presence of relatively rigid bulk molecules. The mobility is found to
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