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CAS RN: 119-64-2 | Product Number: T0107

1,2,3,4-Tetrahydronaphthalene


Purity: >97.0%(GC)
Synonyms:
Product Documents:
25ML
€16.00
1   ≥80 
500ML
€26.00
5   ≥100 

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Product Number T0107
Purity / Analysis Method >97.0%(GC)
Molecular Formula / Molecular Weight C__1__0H__1__2 = 132.21 
Physical State (20 deg.C) Liquid
Storage Temperature Room Temperature (Recommended in a cool and dark place, <15°C)
Store Under Inert Gas Store under inert gas
Condition to Avoid Air Sensitive
CAS RN 119-64-2
Reaxys Registry Number 1446407
PubChem Substance ID 87576117
SDBS (AIST Spectral DB) 907
Merck Index (14) 9221
MDL Number

MFCD00001733

Specifications
Appearance Colorless to Almost colorless clear liquid
Purity(GC) min. 97.0 %
Properties (reference)
Melting Point -36 °C
Boiling Point 207 °C
Flash point 75 °C
Specific Gravity (20/20) 0.97
Refractive Index 1.54
Solubility in water Insoluble
Degree of solubility in water 47 mg/l   28 °C
Solubility (miscible with) Benzene, Alcohol, Ether
GHS
Pictogram Pictogram Pictogram Pictogram
Signal Word Danger
Hazard Statements H302 : Harmful if swallowed.
H315 : Causes skin irritation.
H319 : Causes serious eye irritation.
H373 : May cause damage to organs through prolonged or repeated exposure.
H336 : May cause drowsiness or dizziness.
H304 : May be fatal if swallowed and enters airways.
H411 : Toxic to aquatic life with long lasting effects.
Precautionary Statements P273 : Avoid release to the environment.
P260 : Do not breathe mist or vapours.
P264 : Wash skin thoroughly after handling.
P391 : Collect spillage.
P331 : Do NOT induce vomiting.
P301 + P310 : IF SWALLOWED: Immediately call a POISON CENTER/doctor.
Related Laws:
EC Number 204-340-2
RTECS# QK3850000
Transport Information:
UN Number UN3082
Class 9
Packing Group III
HS Number 2902900000
Application
Preparation of Anhydrous Hydrogen Bromide

Typical procedure: Bromine is slowly added dropwise to a round bottom flask containing a suspension of iron and 1,2,3,4-tetrahydronaphthalene. In the early stage of the reaction, the flask is cooled with water. The reaction is warmed to 30 to 40 ℃ allowing gas evolution. The gas is passed through a wash bottle containing 1,2,3,4-tetrahydronaphthalene in order to eliminate any bromine in the hydrogen bromide. For optimum yields of hydrogen bromide, dry the 1,2,3,4-tetrahydronaphthalene over anhydrous sodium sulfate and then distill it under a dry inert atmosphere (such as argon or nitrogen). If any moisture is introduced into the reaction, the yield of hydrogen bromide becomes remarkably poor.

References

  • Inorg. Synth. 1939, 1, 149.


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