D90601
1,2-Diethylbenzene
technical grade, 92%
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About This Item
Formula condensata:
C6H4(C2H5)2
Numero CAS:
Peso molecolare:
134.22
Beilstein:
1904392
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Grado
technical grade
Saggio
92%
Forma fisica
liquid
Temp. autoaccensione
743 °F
Indice di rifrazione
n20/D 1.502 (lit.)
P. eboll.
183 °C (lit.)
Punto di fusione
−31 °C (lit.)
Densità
0.88 g/mL at 25 °C (lit.)
Stringa SMILE
CCc1ccccc1CC
InChI
1S/C10H14/c1-3-9-7-5-6-8-10(9)4-2/h5-8H,3-4H2,1-2H3
KVNYFPKFSJIPBJ-UHFFFAOYSA-N
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Categorie correlate
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Flam. Liq. 3
Codice della classe di stoccaggio
3 - Flammable liquids
Classe di pericolosità dell'acqua (WGK)
WGK 2
Punto d’infiammabilità (°F)
131.0 °F - closed cup
Punto d’infiammabilità (°C)
55 °C - closed cup
Dispositivi di protezione individuale
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Jean-Paul Payan et al.
Archives of toxicology, 82(9), 591-600 (2008-02-07)
The bio-distribution of the neurotoxic 1,2-diethylbenzene (1,2-DEB) was studied in male Sprague-Dawley rats after intravenous administration of [(14)C] 1,2-DEB (1 mg kg(-1)). The highest concentrations of [(14)C] non-volatile metabolites, determined by whole-body auto-radiography, were in the nasal cavity, ethmoid turbinates
A M Saillenfait et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 37(11), 1089-1096 (1999-11-24)
Sprague-Dawley rats were administered 1,2-diethylbenzene (1,2-DEB) by gavage on gestational days (GD) 6 through 20 at dose levels of 0 (corn oil), 5, 15, 25 or 35 mg/kg. The dams were euthanized on GD21 and the offspring were weighed and
J P Payan et al.
Drug metabolism and disposition: the biological fate of chemicals, 29(6), 868-876 (2001-05-17)
In a previous study, it was shown that the neurotoxic compound 1,2-diethylbenzene (1,2-DEB) is mainly hydroxylated in the alkyl chain to give 1-(2'-ethylphenyl)ethanol (1,2-EPE) and excreted in urine of rats as two glucuronide compounds (GA1 and GA2). Some findings have
I Linhart et al.
Xenobiotica; the fate of foreign compounds in biological systems, 26(12), 1263-1272 (1996-12-01)
1. Biotransformation of 1,2-diethenylbenzene (1) in rat was studied. Five urinary metabolites were isolated by extraction of acid hydrolysed urine and identified by nmr and mass spectroscopy, namely, 1-(2-ethenylphenyl)ethane-1,2-diol (2) 2-ethenylmandelic acid (3), 2-ethenylphenylglyoxylic acid (4), 2-ethenylphenylacetylglycine (5) N-acetyl-S-[1-(2-ethenylphenyl)-2-hydroxyethyl]cysteine (6)
Desire Tshala-Katumbay et al.
Toxicological sciences : an official journal of the Society of Toxicology, 105(1), 134-141 (2008-05-27)
Motor neuron axonopathy in diseases such as amyotrophic lateral sclerosis can be modeled and probed with neurotoxic chemicals that induce similar patterns of pathology, such as axonal spheroids that represent focal accumulation of anterogradely transported neurofilaments (NFs). The aromatic gamma-diketone-like
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