•~»£s^
o Dicyclopentel
Alcohol
*'- -y^K^'^^^p^M^ > *v Molecular Weight Distillation Hange Specific G r a v i t y (25°/25°C.) Iodine INumbcr Hydroxy 1 Number Flash P o i n t (Tag. open cup) Solubility:
ISO
9 5 % between 1U-121°C. at 10 m m . 1.079 169 367 2 I 9 ° C . (126°F.)
Water
Insoluble
Organic Solvents
M i s c i b l e i n all p r o p o r t i o n s w i t h m e t h a n o l , acetone, dioxane, benzene, e t h e r , kerosene, p e t r o l e u m oils, castor o i l .
D i c y c l o p e n t e n v l alcohol undergoes t h e normal reactions of a secontlary alcohol. T h e double bond is s o m e w h a t less reactive t h a n an o r d i n a r y olefin, but under some conditions, will undergo polymerization a n d copolymerization. RCOOH
1. Esferification 2* Oxidation
,CH 2 |
H+ CrOs
-
CH 2 =CH-CN
3. Addition
|CH a .
A\
.
->
H2
4. Hydrogenation
Ni C20H25OH
5. Dimerizafion
(doubly unsaturated dimer)
6. Polymerization
b e n z o y l peroxide
100°C.
(CoH 13 0H)x (viscous oil)
S U G G E S T E D USES 1. Coatings. Derivatives of dicyclopentenyl alcohol, particularly its esters with u n s a t u r a t e d acids, such as t h e m e t h a c r y l a t e or linoleate, and i t s mixed esters, such a s allyl dicyclopentenvl maleate, have interesting air-drying and polymerizing properties. I n general, the dicyclopentenyl group contributes toughness and hardness, with improvement in water and alkali resistance. 2. Other Uses, Dicyclopentenyl alcohol m a y b e of interest in the p r e p a r a t i o n of derivatives for use in the fields of plasticizers, insecticides, oil additives, surface-active agents and solvents.
CHEMICALS
FOR INDUSTRY
WRITE DEPARTMENT
A V A I L A B L E IM PILOT PLANT QUANTITIES
ROHM S- HAAS C O IM W®M>M V WASHINGTON SQUARE, PHILADELPHIA 5, PA. Hepicsentuliivs
in print ipal foreign
countries
SP FOR FREE SAMPLES A N D LITERATURE r***ir.'SL3£--Tri *