ChemicalBook > CAS DataBase List > 1-Methylnaphthalene
1-Methylnaphthalene
1-Methylnaphthalene
- CAS No.90-12-0
- Chemical Name:1-Methylnaphthalene
- CBNumber:CB4127653
- Molecular Formula:C11H10
- Formula Weight:142.2
- MOL File:90-12-0.mol
1-Methylnaphthalene Property
- Melting point −22 °C(lit.)
- Boiling point 240-243 °C(lit.)
- Density 1.001 g/mL at 25 °C(lit.)
- vapor pressure 2 hPa (25 °C)
- refractive index n
20/D 1.615(lit.) - FEMA 3193 | 1-METHYLNAPHTHALENE
- Flash point 180 °F
- storage temp. Store below +30°C.
- solubility 0.026g/l
- pka 37(at 25℃)
- form Liquid
- color Clear colorless to yellow
- Odor at 1.00 % in dipropylene glycol. naphthyl chemical medicinal camphor
- Odor Type naphthyl
- biological source synthetic
- explosive limit 0.7-6.5%(V)
- Water Solubility 0.026 g/L (25 ºC)
- JECFA Number 1335
- BRN 506793
- Dielectric constant 2.7(20℃)
- Exposure limits ACGIH: TWA 0.5 ppm (Skin)
- Stability Stable. Combustible. Incompatible with strong oxidizing agents, oxygen.
- InChIKey QPUYECUOLPXSFR-UHFFFAOYSA-N
- LogP 3.91
- Surface tension 38.6mN/m at 20°C
- Substances Added to Food (formerly EAFUS) 1-METHYLNAPHTHALENE
- CAS DataBase Reference 90-12-0(CAS DataBase Reference)
- FDA UNII E7SK1Y1311
- NIST Chemistry Reference Naphthalene, 1-methyl-(90-12-0)
- EPA Substance Registry System 1-Methylnaphthalene (90-12-0)
- UNSPSC Code 41116107
- NACRES NA.24
Safety
- Hazard Codes :Xn,N,T
- Risk Statements :22-36/37/38-42/43-51/53-39/23/24/25-23/24/25-20/21/22
- Safety Statements :7-26-36/37/39-61-45-36/37-23-36
- RIDADR :UN 3082 9/PG 3
- WGK Germany :2
- RTECS :QJ9630000
- Autoignition Temperature :984 °F
- TSCA :Yes
- HazardClass :9
- PackingGroup :III
- HS Code :29029080
- Hazardous Substances Data :90-12-0(Hazardous Substances Data)
- Toxicity :LD50 orally in Rabbit: 1840 mg/kg
-
NFPA 704:
1 1 0
-
Symbol(GHS)
- Signal wordDanger
- Hazard statements H302-H304-H411
- Precautionary statements P273-P301+P310+P331-P301+P312+P330
1-Methylnaphthalene Price
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- Brand: Sigma-Aldrich(India)
- Product number: W319309
- Product name : 1-Methylnaphthalene
- Purity: ≥95%
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- Price: ₹4880.63
- Updated: 2022/06/14
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- Product number: W319309
- Product name : 1-Methylnaphthalene
- Purity: ≥95%
- Packaging: 100G
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- Brand: Sigma-Aldrich(India)
- Product number: W319309
- Product name : 1-Methylnaphthalene
- Purity: ≥95%
- Packaging: 1KG
- Price: ₹14960.4
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- Brand: Sigma-Aldrich(India)
- Product number: W319309
- Product name : 1-Methylnaphthalene
- Purity: ≥95%
- Packaging: 5KG
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- Product number: M56808
- Product name : 1-Methylnaphthalene
- Purity: 95%
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1-Methylnaphthalene Chemical Properties,Usage,Production
- Description 1-methylnaphthalene is a methylnaphthalene carrying a methyl substituent at position. It is a polycyclic aromatic hydrocarbon (PAH). It is present in cigarette smoke, wood smoke, tar, asphalt, and at some hazardous waste sites. The main use of 1-methylnaphthalene is as a raw material for naphthoic acid, fluorescent whitening agents, and surfactants. It is also used as a raw material for dyestuff dispersants and heat transfer oils, and as a solvent for agricultural chemical.
- Chemical Properties 1-methylnaphthalene is a colorless, bluefluorescing liquid with an earthy, phenolic odor. It is insoluble in water but dissolves in alcohol and ether. With a density greater than water, this combustible substance is obtained from coal tar and used in organic synthesis. It has a role as a carcinogenic agent and a plant metabolite.
- Occurrence Methylnaphthalene was identified as a volatile component of cassava, roasted filberts and nectarines. Assorted types of lima, pinto, red kidney, black, navy and mung beans, soybeans, split peas and lentils were found to contain 1-methylnaphthalene at concentrations ranging from 2.8 to 49.2 ppb.
- Uses The main uses of methylnaphthalene are as a raw material for dyestuff dispersants and heat transfer oils, and as a solvent for agricultural chemical. It is used in insecticide manufacturing; manufacture of phthalic anhydride; solvent in organic synthesis; asphalt and naptha constituent. It is also used as a test substance for the determination of the cetane number of diesel fuels. Further, it is employed in the preparation of 1-methylnaphthalene-d10 using deuterium oxide, sodium deuteroxide.
- 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.
- Preparation 1-Methylnaphthalene is primarily derived from coal tar and petroleum oils. It is present in high-temperature coal tar in a concentration of 0.5% and is produced industrially from the methylnaphthalene fraction, which boils between 240 and 245 °C, by redistillation of the 2-methylnaphthalene filtrate following crystallization and separation of 2-methylnaphthalene.
- Aroma threshold values Detection: 7.5 to 20 ppb.
- Taste threshold values Taste characteristics at 1 ppm: naphthyl-like with a medicinal nuance.
-
Synthesis Reference(s)
Journal of the American Chemical Society, 65, p. 295, 1943 DOI: 10.1021/ja01242a503
The Journal of Organic Chemistry, 53, p. 4466, 1988 DOI: 10.1021/jo00254a009
Tetrahedron Letters, 29, p. 97, 1988 DOI: 10.1016/0040-4039(88)80026-1 - General Description 1-methylnaphthalene is a colorless liquid. Freezing point -22 °C (7.6 °F). Boiling point 240-243 °C (464-469 °F). Flash point 82 °C (180 °F). Denser than water. Derived from coal tar and used in organic synthesis.
- Air & Water Reactions Insoluble in water.
- Reactivity Profile 1-Methylnaphthalene is sensitive to heat. Reacts with strong oxidizing agents. Incompatible with oxygen and peroxides .
- Hazard Moderate fire risk. Lower respiratory tractirritant and lung damage. Questionable carcinogen.
- Health Hazard Harmful if inhaled. Liquid causes irritation of the eyes and skin and skin photosensitization. Harmful if swallowed. Chronic exposure may cause liver or kidney damage.
- Fire Hazard 1-Methylnaphthalene is combustible.
- Carcinogenicity The carcinogenic potential of 1- and 2-methyl was investigated in B6C3F1 mice. Female and male mice were given methylnaphthalene in their diets for 81 weeks. The results indicated that 1-methyl was a possible weak carcinogen in the lung of male but not female mice whereas 2-methyl did not possess unequivocal carcinogenic potential in these mice.
- Purification Methods Dry 1-methylnaphthalene for several days with CaCl2 or by prolonged refluxing with BaO. Fractionally distil it through a glass helices-packed column from sodium. Purify it further by solution in MeOH and precipitation of its picrate complex by adding to a saturated solution of picric acid in MeOH. The picrate, after crystallisation to constant melting point (m 140-141o) from MeOH, is dissolved in *benzene and extracted with aqueous 10% LiOH until the extract is colourless. Evaporation of the *benzene solution under vacuum gives 1-methylnaphthalene [Kloetzel & Herzog J Am Chem Soc 72 1991 1950]. However, neither the picrate nor the styphnate complexes satisfactorily separate 1-and 2-methylnaphthalenes. To achieve this, 2-methylnaphthalene (10.7g) in 95% EtOH (50mL) has been precipitated with 1,3,5-trinitrobenzene (7.8g) and this complex has been crystallised from MeOH to m 153-153.5o (m of the 2-methyl isomer is 124o). [Alternatively, 2,4,7-trinitrofluorenone in hot glacial acetic acid could be used, and the derivative (m 163-164o) is recrystallised from glacial acetic acid]. The 1-methylnaphthalene is regenerated by passing a soution of the complex in dry *benzene through a 15-in column of activated alumina and washing with *benzene/pet ether (b 35-60o) until the coloured band of the nitro compound had moved down near the end of the column. The complex can also be decomposed using tin and acetic-hydrochloric acids, followed by extraction with diethyl ether and *benzene; the extracts are washed successively with dilute HCl, strongly alkaline sodium hypophosphite, water, dilute HCl and water. [Soffer & Stewart J Am Chem Soc 74 567 1952.] It can be freed from anthracene by zone melting [Beilstein 5 IV 1687.]
- Toxics Screening Level The current ITSL for 1-methylnaphthalene (250 μg/m3) has a justification (attached) dated April 28, 2008. The averaging time (AT) assigned at that time was 24 hours, as per the default methodology (Rule 232(2)(b))
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