ChemicalBook--->CAS DataBase List--->1321-94-4

1321-94-4

1321-94-4 Structure

1321-94-4 Structure
IdentificationBack Directory
[Name]

Methylnaphthalene
[CAS]

1321-94-4
[Synonyms]

dycar mn
tetrosin mnlf
methylnaftalen
MEHYL NAPHTHALENE
methyl-naphthalen
Methylnaphthalene
Naphthalene, methyl-
monomethylnaphthalene
Mixed Methylnaphthalene
1(or2)-Methylnaphthalene
ALPHA/B-Methylnaphthalene
Methylnaphthalene ISO 9001:2015 REACH
[EINECS(EC#)]

215-329-7
[Molecular Formula]

C11H10
[MDL Number]

MFCD00004034
[MOL File]

1321-94-4.mol
[Molecular Weight]

142.197
Questions And AnswerBack Directory
[Preparation]

Preparation of 1-Methylnaphthalene
The methylnaphthalene fraction with a distillation range of 240-245℃ is separated from the wash oil fraction of the distillation. The methylnaphthalene fraction is cooled to -20℃, and crude 2-methylnaphthalene crystals are separated. The resulting mother liquor is used to extract 1-methylnaphthalene. After sulfonation with 95-98% concentrated sulfuric acid, the unsulfonated oil is separated and removed. Then, water is added for dilution, and 1-methylnaphthalene sulfonic acid crystals are precipitated at 10℃. After filtration of the crystals, they are hydrolyzed with superheated steam at 125-150℃ to remove the aqueous layer, yielding industrial-grade 1-methylnaphthalene with a purity of 85-90%. Repeated sulfonation and hydrolysis of industrial-grade 1-methylnaphthalene 2-3 times can yield 1-methylnaphthalene with a purity greater than 98%.
Preparation of 2-Methylnaphthalene
The methylnaphthalene fraction with a distillation range of 240–245 °C is separated from the wash oil fraction of the distillation. The methylnaphthalene fraction is cooled to -20 °C to separate crude 2-methylnaphthalene crystals. The crude 2-methylnaphthalene is recrystallized from ethanol or methanol. The obtained crystals are centrifuged and heated to melt and filter to remove impurities, yielding 2-methylnaphthalene with a purity of over 97%.
[Application]

1-Methylnaphthalene is used as a surfactant, heat transfer fluid, pharmaceutical intermediate, and sulfur extractant for vinyl chloride fiber and polyester dyeing carriers. It can also be used in the production of plasticizers and fiber dyeing auxiliaries. It can also be used as a diesel cetane number tester, a solvent for pesticides, and a solvent for anthraquinone hydrogen peroxide production. It can also be used to produce the plant growth regulator 1-naphthaleneacetic acid. 2-Methylnaphthalene is mainly used in the production of vitamin K3, polyester fiber chromosome carriers, fiber dyeing auxiliaries, organic pigments, concrete additives, detergents, emulsifiers, hemostatic agents, wetting agents, plant growth regulators, beverage additives, feed additives, oral contraceptives, and color film dyes. 3. Mixed Methylnaphthalene can be used as a raw material for pharmaceuticals and surfactants. Furthermore, methylnaphthalene can be catalyzed with HF/BF3 to prepare mesophase pitch, which is a high-quality raw material for carbon fiber production.
Chemical PropertiesBack Directory
[Melting point ]

34°C
[Boiling point ]

229.78°C (estimate)
[density ]

1.0381 (estimate)
[refractive index ]

1.6085 (estimate)
[EPA Substance Registry System]

Methylnaphthalene (1321-94-4)
Safety DataBack Directory
[RIDADR ]

3082
[TSCA ]

TSCA listed
[HazardClass ]

9
[PackingGroup ]

III
[Hazardous Substances Data]

1321-94-4(Hazardous Substances Data)
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Sodium hydroxide-->Sulfuric acid-->Ethylene tar
[Preparation Products]

Menadione-->Sodium poly[(naphthaleneformaldehyde)sulfonate]-->Vitamin K1-->Menadiol diacetate-->Dispersant DDA881
Hazard InformationBack Directory
[Definition]

ChEBI: 1-methylnaphthalene is a methylnaphthalene carrying a methyl substituent at position 1. It has a role as a carcinogenic agent and a plant metabolite.
[General Description]

Bluish-brown oil or a clear yellow liquid. Coal tar or mothball odor.
[Air & Water Reactions]

Insoluble in water.
[Reactivity Profile]

Methylnaphthalene is incompatible with strong oxidizing agents. Methylnaphthalene is also incompatible with peroxides and oxygen.
[Fire Hazard]

Methylnaphthalene is probably combustible.
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