acenaphthylene cyclopenta(de)naphthalene Cyclopenta
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4.Method of Aanlysis(MOA)
5.Nuclear Magnetic Resonance(NMR)
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Product Name: | ACENAPHTHYLENE |
Synonyms: | ACENAPHTHALENE;ACENAPHTHYLENE;acenaphthylene,industrial;cyclopenta(de)naphthalene;Cyclopenta[de]naphthalene;ACENAPHTHYLENE, 99+%;ACENAPHTHYLENE, 100MG, NEAT;ACENAPHTHYLENE, 1X1ML, MEOH, 5000UG/ML |
CAS: | 208-96-8 |
MF: | C12H8 |
MW: | 152.19 |
EINECS: | 205-917-1 |
Product Categories: | Industrial/Fine Chemicals;AA to ALAnalytical Standards;A;A-BAlphabetic;Alpha Sort;AromaticsChemical Class;Chemical Class;Hydrocarbons;NeatsAnalytical Standards;PAHs;Volatiles/ Semivolatiles;Arenes;Building Blocks;Organic Building Blocks;Naphthalenes;AA to AL;Alphabetic;Aromatics;Mutagenesis Research Chemicals;Building Blocks;Chemical Synthesis;Organic Building Blocks;PAH |
Mol File: | 208-96-8.mol |
ACENAPHTHYLENE Chemical Properties |
mp | 78-82 °C(lit.) |
bp | 280 °C(lit.) |
density | 0.899 g/mL at 25 °C(lit.) |
Fp | 122°C |
storage temp. | APPROX 4°C |
BRN | 774092 |
Stability: | Stable. Incompatible with oxidizing agents. |
CAS DataBase Reference | 208-96-8(CAS DataBase Reference) |
Safety Information |
Hazard Codes | Xn,N,F,T,Xi |
Risk Statements | 22-36/37/38-67-65-50/53-38-11-39/23/24/25-23/24/25-20 |
Safety Statements | 26-36/37/39-62-61-60-45-36/37-16-7-37/39-33-25-9 |
RIDADR | UN 1145 3/PG 2 |
WGK Germany | 3 |
RTECS | AB1254000 |
MSDS Information |
Provider | Language |
---|---|
SigmaAldrich | English |
ACROS | English |
ALFA | English |
ACENAPHTHYLENE Usage And Synthesis |
Chemical Properties | yellow crystalline powder |
Usage | Polycyclic aromatic hydrocarbons as carcinogenic |
General Description | Colorless crystalline solid. Insoluble in water. Used in dye synthesis, insecticides, fungicides, and in the manufacture of plastics. |
Air & Water Reactions | Insoluble in water. |
Reactivity Profile | Vigorous reactions, sometimes amounting to explosions, can result from the contact between aromatic hydrocarbons, such as ACENAPHTHYLENE, and strong oxidizing agents. They can react exothermically with bases and with diazo compounds. Substitution at the benzene nucleus occurs by halogenation (acid catalyst), nitration, sulfonation, and the Friedel-Crafts reaction. |
ACENAPHTHYLENE Preparation Products And Raw materials |
Preparation Products | 4-AMINO-1,8-NAPHTHALIMIDE-->1-ACETOXYACENAPHTHENE |
Raw materials | Calcium oxide-->Potassium sulfate -->Polishing oil-->Acenaphthene--> |
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