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Xylol, Isomerengemisch

1,2-Xylene; 1,3-xylene; 1,4-xylene

HCID 6850715
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GrundinformationenÜberblickNamen und BezeichnerEigenschaftenSicherheit und RegulatorischesChemie und IndustrieZugehörige ReaktionenNotizen zur Verbindung
TeilstruktursucheÄhnliche Strukturen suchen

Grundinformationen

CAS
1330-20-7
Standard-SMILES
Cc1ccc(C)cc1.Cc1cccc(C)c1.Cc1ccccc1C
InChIKey
MVZVDAGWAAZJPE-UHFFFAOYSA-N
Summenformel
C24H30
Durchschnittliche Molmasse
318,5 g/mol

Überblick

See also: Xylene (annotation moved to).

Namen und Bezeichner

Bevorzugter Name
1,2-Xylene; 1,3-xylene; 1,4-xylene
IUPAC
1,2-xylene;1,3-xylene;1,4-xylene
Lokaler Name
Xylol, Isomerengemisch
Englischer Name
Xylene
Summenformel
C8H10
Molmasse
106.17

Namen und Synonyme

1,2-xylene; 1,3-xylene; 1,4-xyleneRefChem:412235905-215-11,2-xylene;1,3-xylene;1,4-xyleneXylenes, ACS reagent, >=98.5% xylenes + ethylbenzene basisXylenes reagentXylenes, ACS reagentXylenes, reagent gradeXylenes, histological gradeXylenes, puriss., 98.0%SCHEMBL2091251Xylene, mixed isomers, >98%
Weitere Namen anzeigen
XYLENESXyLMIXED XYLENEDIMETHYLBENZENEXYLOLxylenenXYLENES, MIXEDNAPHTHA SOLVENTbenzene,dimethyl-SCINTILENE COCKTAIL
SCHEMBL29376029Xylenes, AR, sulfur free, >=99%Xylenes, LR, sulfur free, >=98%AKOS026745417Xylenes, SAJ first grade, >=80.0%Xylenes, SAJ special grade, >=80.0%ST50406765Dimethylbenzene; Entellan New; Xylol; ZEP-RD;

Datenbank-Bezeichner

CAS
1330-20-7

Eigenschaften

Berechnete StruktureigenschaftenWird ergänzt

Polarare Oberfläche (TPSA)
0 Ų
H-Brücken-Donoren
0
H-Brücken-Akzeptoren
0
Frei drehbare Bindungen
0
Schwere Atome
24
Formalladung
0
Komplexität
163

Physikochemische Eigenschaften

Schmelzpunkt
-34 °C · -34 °C
Siedepunkt
137 · 137-140 °C (lit.)
Dichte
0.86 g/mL · 0.86 g/mL at 25 °C (lit.)
Dampfdichte
3.7 · 3.7 (vs air)
Dampfdruck
18 mm · 18 mm Hg ( 37.7 °C)
Brechungsindex
20 · n20/D 1.497(lit.)
Flammpunkt
77 °F · 77 °F(lit.)
storage temp.
Flammables area
Löslichkeit
Chloroform (Soluble), Methanol (Slightly)
Aggregatzustand
Liquid
Farbe
10 · APHA: ≤10
Geruch (Odor)
char. sweet odor
Explosionsgrenze
7 % · 7%
Wasserlöslichkeit
0.1 g/L · <0.1 g/L (20 ºC)
Merck
14 · 14,10081
BRN
1901563 · 1901563

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

GHS-Klassifizierung

GHS Classification · 4 Einträge

Warning

H226 (100%): Flammable liquid and vapor [Warning Flammable liquids]

P210, P233, P240, P241, P242, P243, P261, P264, P271, P280, P302+P352, P303+P361+P353, P304+P340, P317, P321, P332+P317, P362+P364, P370+P378, P403+P235, and P501 (click each P-code to see the statement)

The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

Gefahrenhinweise

Hazard Classes and CategoriesFlam. Liq. 3 (100%)

Sicherheitsdaten

OEB
A
OEL
TWA: 100.0 ppm; 435.0 mg/m3, STEL: 150.0 ppm; 655.0 mg/m3
wgk
2
tsca
TSCA listed
ridadr
UN 1307 3/PG II/III (XYLENES)
hs_code
29024400
RTECS-Nr.
ZE2100000
risk_code
10-20/21-38-36/38-65-48/20
Toxizität
LD50 oral in rat: 4300mg/kg
hazard_code
Xn,F
safety_code
25-36/37-62
hazard_class
3
packing_group
II
Speicherklasse
3 - Flammable liquids
Giftige Stoffe Daten
1330-20-7(Hazardous Substances Data)

Chemie und Industrie

Anwendungen · 2 Einträge

BeschreibungXylene is used as a solvent. In this application, the mixture of isomers is often referred to as xylenes or xylol. Solvent xylene often contains a small percentage of ethylbenzene. Like the individual isomers, the mixture is colourless, sweet smelling, and highly flammable. Application of xylene is extensive and includes, but is not limited to, printing, rubber, and leather industries. Similarly, it is used as a cleaning agent for steel and silicon wafers. In the petroleum industry, xylene is also a frequent component of paraffin solvents, used when the tubing becomes clogged with paraffin wax. Xylene is incompatible with strong oxidisers and is known to cause fires and explosions. There are three forms of xylene in which the methyl groups vary on the benzene ring: (i) meta-xylene, (ii) ortho-xylene, and (iii) para-xylene. These forms are referred to as isomers. Xylene is a colourless, sweet-smelling liquid. Xylene occurs naturally in petroleum and coal tar. Chemical industries produce xylene from petroleum. It is also used as a cleaning agent and a thinner for paint and in paints, in glues, in printing inks, and in varnishes. Xylene evaporates quickly from the soil and surface water into the air.

VerwendenXylene is used as a chemical feedstock in the chemical industry. Xylenes can undergooxidation where the side methyl groups are oxidized to give a carboxyl group (COOH)yielding a carboxylic acid. The particular acid produced depends on the isomer oxidized. Wheno-xylene is oxidized phthalic acid is produced, and when p-xylene is oxidized terephthalic acidresults. Terephthalic acid is one of the main feedstocks in making polyesters.Terephthalic acid reacts with ethylene glycol to form the ester polyethylene terephthalate(PET). PET is one of the most common plastics used as food and beverage containers. PETcontainers contain the recycling symbol with a number 1. PET is marketed using a numberof commercial names; the most generic of these is polyester. It is also the material known asDacron. Mylar is PET in the form of thin films. Although all three isomers of xylene are usedas chemical feedstocks, the greatest demand is for para-xylene to produce terephthalic acid.The smallest demand is for meta-xylene. Approximately 30 million tons of xylenes are usedannually worldwide.

Vor- und nachgelagerte Produkte

Vorgelagerte Rohstoffe

Diethylenglykol

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Auf dieser SeiteGrundinformationenÜberblickNamen und BezeichnerEigenschaftenSicherheit und RegulatorischesChemie und IndustrieZugehörige ReaktionenNotizen zur Verbindung
PubChem CID
6850715
EC Number
905-215-1
Dielectric constant
10 · 10.0(Ambient)
Stabilität
Volatile, flammable and its vapors form explosive mixtures with air at room temperature.
Kosmetik-Inhaltsstoffe Funktionen
SOLVENTFRAGRANCEPERFUMING
InChI
1S/3C8H10/c1-7-3-5-8(2)6-4-7;1-7-4-3-5-8(2)6-7;1-7-5-3-4-6-8(7)2/h3*3-6H,1-2H3
InChIKey
KAKOUNRRKSHVJO-UHFFFAOYSA-N
SMILES
Cc1ccc(C)cc1.Cc2cccc(C)c2.Cc3ccccc3C
LogP
3.16 at · 3.16 at 20℃
CAS Datenbank
1330 · 1330-20-7(CAS DataBase Reference)
EPA chemische Informationen
Xylene (1330-20-7)
ECETOC JACC REPORT
Xylene (1330-20-7)
Hazard Classifications
Acute Tox. 4 DermalAcute Tox. 4 InhalationAquatic Chronic 3Asp. Tox. 1Eye Irrit. 2Flam. Liq. 3Skin Irrit. 2STOT RE 2 InhalationSTOT SE 3
Selbstentzündungstemperatur
867 °F
Platin
Motor benzol
heavy benzol
Hydrogenated gasoline
light benzol
Naphtha
COUMARONE RESIN
Natriumhydroxid
Poly(acrylic acid)
Calcium chloride hexahydrate
Schwefelsure

Nachgelagerte Produkte

pesticide emulsifier BSLpolyurethane water-based emulsion finishes PU-II seriesCHLOROMETHYL ISO-PROPYL ETHERPropisochlorPesticide emulsifier 0207Fenvalerate+Malathion,E.C.(21%)3-(Benzyloxy)phenolreversible temperature indicating coating (IV)TolualdehydN,N'-DiphenylbenzidinAsphalt antifouling paint L40-32pesticide emuslsifier 656Lp-Phenylenbis(methylamin)2-Chlor-N-(2,6-dimethylphenyl)-N-(1H-pyrazol-1-ylmethyl)acetamid4,6-Dimethyl-2-pyridylaminVat Voilet 3N-ACETYLHOMOPIPERAZINEAmino resin varnishpesticide emulsifier 6502biodegrddable finishing agent for fabricSantalolpesticide emulsifier 0206SantalylacetatCHLOROMETHYL BUTYL ETHERPyridaben E.C.Malathion+Fenitrothion,E.C.ETHYLENESULFATEQuizalofop-ethyl E.C.DiethylbenzolAcrylic acid maleic acid copolymer(2,6-Diisopropyl-4-Phenoxy)PhenylthioureaAmino baking varnish[3R-(3α,3aβ,6β,7β,8aα)]-Octahydro-6-methoxy-3,6,8,8-tetramethyl-1H-3a,7-methanoazulenN-Methyl-1-(methylthio)-2-nitrovinylaminXylidinEthyl-2,3-epoxy-3-phenylbutyrat4-PROPYL-PYRIDIN-2-YLAMINEMethyl 3-isoquinolinecarboxylatepesticide emulsifier BCLfire resistant silicone sealant LZ-850

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Ergänzende Hinweise · 1 Eintrag

DefinitionAn organic hydrocarbon present in the light-oil fraction of crude oil. It is used extensively as a solvent. There are three isomeric compounds with this name and formula, distinguished as 1,2-, 1,3-, and 1,4-dimethylbenzene according to the positions of the methyl groups on the benzene ring.