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m-Xylene

m-Xylene Structure
CAS No.
108-38-3
Chemical Name:
m-Xylene
Synonyms
1,3-Xylene;1,3-DIMETHYLBENZENE;3-xylene;m-Xylol;META-XYLENE;Benzene,1,3-dimethyl-;2,4-Xylene;3-methyltoluene;m-XyL;M-XYLENE
CBNumber:
CB4852746
Molecular Formula:
C8H10
Molecular Weight:
106.17
MOL File:
108-38-3.mol
MSDS File:
SDS
Modify Date:
2024/3/14 15:18:26

m-Xylene Properties

Melting point -48 °C (lit.)
Boiling point 138-139 °C (lit.)
Density 0.868 g/mL at 25 °C (lit.)
vapor density 3.7 (vs air)
vapor pressure 16 mm Hg ( 37.7 °C)
refractive index n20/D 1.497(lit.)
Flash point 77 °F
storage temp. 2-8°C
solubility Miscible with many organic solvents, including alcohol and ether
form Liquid
pka >15 (Christensen et al., 1975)
color Colorless
Odor Like benzene; characteristic aromatic.
Odor Threshold 0.041ppm
explosive limit 1.1-7%(V)
Water Solubility Miscible with organic solvents. Immiscible with water.
Merck 14,10081
BRN 605441
Henry's Law Constant 14.80 at 45.00 °C, 17.26.4 at 50.00 °C, 19.90 at 55.00 °C, 23.01.3 at 60.00 °C, 27.46.3 at 70.00 °C (static headspace-GC, Park et al., 2004)
Exposure limits NIOSH REL: 100 ppm (435 mg/m3), STEL 150 ppm (655 mg/m3), IDLH 900 ppm; OSHA PEL: TWA 100 ppm; ACGIH TLV: TWA 100 ppm, STEL 150 ppm (adopted).
Dielectric constant 2.3999999999999999
InChIKey IVSZLXZYQVIEFR-UHFFFAOYSA-N
LogP 3.16 at 20℃
CAS DataBase Reference 108-38-3(CAS DataBase Reference)
NIST Chemistry Reference Benzene, 1,3-dimethyl-(108-38-3)
EPA Substance Registry System m-Xylene (108-38-3)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS02,GHS07,GHS08
Signal word  Danger
Hazard statements  H226-H304-H312+H332-H315-H319-H335-H412
Precautionary statements  P210-P273-P280-P301+P310-P303+P361+P353-P331
Hazard Codes  Xn,T,F
Risk Statements  10-20/21-38-39/23/24/25-23/24/25-11-36/38
Safety Statements  25-45-36/37-16-7
RIDADR  UN 1307 3/PG 3
OEB A
OEL TWA: 100 ppm (435 mg/m3), STEL: 150 ppm (655 mg/m3)
WGK Germany  2
RTECS  ZE2275000
Autoignition Temperature 982 °F
TSCA  Yes
HazardClass  3
PackingGroup  II
HS Code  29024200
Toxicity LD50 orally in rats: 7.71 ml/kg (Smyth)
NFPA 704
3
2 0

m-Xylene price More Price(21)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) RTC000101 m-Xylene Pharmaceutical Secondary Standard; Certified Reference Material 108-38-3 20ML ₹11723.78 2022-06-14 Buy
Sigma-Aldrich(India) 95672 m-Xylene puriss. p.a., ≥99.0% (GC) 108-38-3 1L ₹13799.33 2022-06-14 Buy
Sigma-Aldrich(India) PHR1313 m-Xylene Pharmaceutical Secondary Standard; Certified Reference Material 108-38-3 1G ₹11682.68 2022-06-14 Buy
Sigma-Aldrich(India) 95672 m-Xylene puriss. p.a., ≥99.0% (GC) 108-38-3 2.5L ₹20149.28 2022-06-14 Buy
Sigma-Aldrich(India) 95670 m-Xylene analytical standard 108-38-3 5ML ₹9124.2 2022-06-14 Buy
Product number Packaging Price Buy
RTC000101 20ML ₹11723.78 Buy
95672 1L ₹13799.33 Buy
PHR1313 1G ₹11682.68 Buy
95672 2.5L ₹20149.28 Buy
95670 5ML ₹9124.2 Buy

m-Xylene Chemical Properties,Uses,Production

Chemical Properties

Xylene exists in three isomeric forms, ortho-, meta-, and para-xylene. Commercial xylene is a mixture of these three isomers and may also contain ethylbenzene as well as small amounts of toluene, trimethylbenzene, phenol, thiophene, pyridine, and other nonaromatic hydrocarbons. m-Xylene is predominant in commercial xylene.

Physical properties

Clear, colorless, watery liquid with a sweet, aromatic odor. An odor threshold concentration of 48 ppbv was reported by Nagata and Takeuchi (1990).

Uses

m-Xylene is used in the production of isophthalic acid, which is a monomer and utilized in preparation of polyethylene terephthalate. It is used as an important starting material in the production of 2,4- and 2,6-xylidine. It is used as solvent in histology.

Definition

ChEBI: A xylene carrying methyl groups at positions 1 and 3.

General Description

A colorless watery liquid with a sweet odor. Less dense than water. Insoluble in water. Irritating vapor.

Air & Water Reactions

Highly flammable. Insoluble in water.

Reactivity Profile

m-Xylene may react with oxidizing materials. .

Health Hazard

Vapors cause headache and dizziness. Liquid irritates eyes and skin. If taken into lungs, causes severe coughing, distress, and rapidly developing pulmonary edema. If ingested, causes nausea, vomiting, cramps, headache, and coma; can be fatal. Kidney and liver damage can occur.

Fire Hazard

Behavior in Fire: Vapor is heavier than air and may travel considerable distance to a source of ignition and flash back.

Chemical Reactivity

Reactivity with Water No reaction; Reactivity with Common Materials: No reaction; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.

Safety Profile

Moderately toxic by intraperitoneal route. Wdly toxic by ingestion, skin contact, and inhalation. An experimental teratogen. Human systemic effects by inhalation: motor activity changes, ataxia, and irritabihty. Experimental reproductive effects. A severe skin irritant. A common air contaminant. A very dangerous fire hazard when exposed to heat or flame; can react with oxidzing materials. Explosive in the form of vapor when exposed to heat or flame. To fight fire, use foam, CO2, dry chemical. Emitted from modern building materials (CENEAR 69,22,91). When heated to decomposition it emits acrid smoke and irritating fumes. See also other xylene entries.

Potential Exposure

Xylene is used as a solvent; as a constituent of paint, lacquers, varnishes, inks, dyes, adhesives, cements, cleaning fluids, and aviation fuels; and as a chemical feed-stock for xylidines, benzoic acid; phthalic anhydride; isophthalic, and terephthalic acids; as well as their esters (which are specifically used in the manufacture of plastic materials and synthetic textile fabrics). Xylene is also used in the manufacture of quartz crystal oscillators, hydrogen peroxide; perfumes, insect repellants; epoxy resins; pharmaceuticals; and in the leather industry. m-Xylene is used as an intermediate in preparation of isophthalic acid; o-xylene is used in manufacture of phthalic anhydride and in pharmaceutical and insecticide synthesis. p-xylene is used in pharmaceutical and insecticide synthesis and in production of polyester.

Shipping

UN1307 Xylenes, Hazard Class: 3; Labels: 3-Flammable liquid.

Purification Methods

The general purification methods listed under xylene are applicable. The o-and p-isomers can be removed by their selective oxidation when a m-xylene sample containing them is boiled with dilute HNO3 (one part conc acid to three parts water). After washing with water and alkali, the product can be steam distilled, collected as for o-xylene, then distilled and purified further by sulfonation. [Clarke & Taylor J Am Chem Soc 45 831 1923.] m-Xylene is selectively sulfonated when a mixture of xylenes is refluxed with the theoretical amount of 50-70% H2SO4 at 85-95o under reduced pressure. By using a still resembling a Dean and Stark apparatus, water in the condensate can be progressively withdrawn while the xylene is returned to the reaction vessel. After cooling, then adding water, unreacted xylenes are distilled off under reduced pressure. The m-xylene sulfonic acid is subsequently hydrolysed by steam distillation up to 140o, the free m-xylene is washed, dried with silica gel and again distilled. It is stored over molecular sieves Linde type 4A. [Beilstein 5 H 370, 5 I 182, 5 II 287, 5 III 823, 5 IV 932.]

Incompatibilities

Vapor may form explosive mixture with air. Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, and epoxides. Electrostatic charges can be generated from agitation or flow.

Waste Disposal

Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal. Incineration.

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