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1-Methylnaphthalene

Product Name
1-Methylnaphthalene
CAS No.
90-12-0
Chemical Name
1-Methylnaphthalene
Synonyms
Α-METHYLNAPHTHALENE;Naphthalene,1-methyl-;ALPHA-METHYLNAPHTHALENE;FEMA 3193;femanumber3193;1-Methylnaphth;1-Methylphthalene;1-Methylnaphthene;1-methyl-naphthalen;A-METHYLNAPHTHALENE
CBNumber
CB4127653
Molecular Formula
C11H10
Formula Weight
142.2
MOL File
90-12-0.mol
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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)
FEMA 
3193 | 1-METHYLNAPHTHALENE
refractive index 
n20/D 1.615(lit.)
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
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
CAS DataBase Reference
90-12-0(CAS DataBase Reference)
NIST Chemistry Reference
Naphthalene, 1-methyl-(90-12-0)
EPA Substance Registry System
1-Methylnaphthalene (90-12-0)
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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
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H302Harmful if swallowed

H304May be fatal if swallowed and enters airways

H411Toxic to aquatic life with long lasting effects

Precautionary statements

P273Avoid release to the environment.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
W319309
Product name
1-Methylnaphthalene
Purity
≥95%
Packaging
1kg
Price
$157
Updated
2024/03/01
Sigma-Aldrich
Product number
W319309
Product name
1-Methylnaphthalene
Purity
≥95%
Packaging
5kg
Price
$470
Updated
2024/03/01
Sigma-Aldrich
Product number
8.20809
Product name
1-Methylnaphthalene
Purity
for synthesis
Packaging
5ml
Price
$34.6
Updated
2024/03/01
Sigma-Aldrich
Product number
8.20809
Product name
1-Methylnaphthalene
Purity
for synthesis
Packaging
250ML
Price
$69.1
Updated
2024/03/01
Sigma-Aldrich
Product number
8.20809
Product name
1-Methylnaphthalene
Purity
for synthesis
Packaging
1L
Price
$223
Updated
2024/03/01
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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.

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.

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.

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.]

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1-Methylnaphthalene Suppliers

SHANGHAI BANGCHENG CHEMICAL Co.,Ltd.
Tel
021-69106960 13701823733
Fax
021-69106780
Email
13701823733@163.com
Country
China
ProdList
4775
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60
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
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China
ProdList
30132
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TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24539
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81
Energy Chemical
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021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
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China
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44751
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Shanghai Longsheng chemical Co.,Ltd.
Tel
021-58099652-8005 13585536065
Fax
021-58099609
Email
bin.wu@shlschem.com
Country
China
ProdList
9816
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Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696;
Email
info@hanhongsci.com
Country
China
ProdList
42982
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Syntechem Co.,Ltd
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Fax
E-Mail Inquiry
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info@syntechem.com
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China
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BEST-REAGENT
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400-1166-196 18981987031
Fax
028-84555506 800101999
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cdhxsj@163.com
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China
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11726
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China Langchem Inc.
Tel
0086-21-58956006
Fax
0086-21-58956100
Country
China
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7815
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Tianjin heowns Biochemical Technology Co., Ltd.
Tel
400 638 7771
Email
sales@heowns.com
Country
China
ProdList
14443
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View Lastest Price from 1-Methylnaphthalene manufacturers

Henan Fengda Chemical Co., Ltd
Product
1-Methylnaphthalene 90-12-0
Price
US $100.00-1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
g-kg-tons, free sample is available
Release date
2023-12-25
Hebei Mojin Biotechnology Co., Ltd
Product
1-Methylnaphthalene 90-12-0
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
50000KG/month
Release date
2023-08-23
Baoji Guokang Bio-Technology Co., Ltd.
Product
1-Methylnaphthalene 90-12-0
Price
US $20.00/KG
Min. Order
25Kg/Drum
Purity
96%
Supply Ability
100T
Release date
2021-06-02

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