n -propylphenols

n -propylphenols
Surname	2- n -propylphenol	3- n -propylphenol	4- n -propylphenol
Structural formula
CAS number	644-35-9	621-27-2	645-56-7
PubChem	12570	69302	12580
Molecular formula	C 9 H 12 O
Molar mass	136.19 g mol −1
Physical state	liquid	firmly
description	oily liquid
Melting point		26 ° C	22 ° C
boiling point	224-226 ° C	229-231 ° C	232 ° C
density	0.989 g cm −3 (20 ° C)	0.95 g cm −3	0.983 g cm −3 (25 ° C)
GHS labeling	Caution	danger	Caution
H and P phrases	302-312-315-319-332-335	302-312-314	302-312-315-319-332-335
	no EUH phrases	no EUH phrases	no EUH phrases
	261-280-305 + 351 + 338	260-303 + 361 + 353-305 + 351 + 338 301 + 330 + 331-405-501	261-280-305 + 351 + 338

In chemistry, the n- propylphenols form a group of substances that are derived from both phenol and n- propylbenzene . The structure consists of a benzene ring with attached hydroxyl group  (-OH) and n -propyl group  (-CH ₂ -CH ₂ -CH ₃ ) as substituents . Their different arrangement results in three constitutional isomers with the empirical formula C ₉ H ₁₂ O.

properties

3- n -Propylphenol gives iron (III) chloride in ethanol a green color, in water a bluish color. The methyl ethers, the n- propyl anisoles, are formed by methylation with dimethyl sulfate .

Individual evidence

1. ^ ^{A b c} Heilbron: Dictionary of Organic Compounds , Volume Four, 1953 , p. 255; Full text .
2. ↑ ^{a b} Zvi Rappoport (Ed.): CRC Handbook of Tables for Organic Compound Identification . 3 ^rd Edition, CRC Press / Taylor and Francis, Boca Raton, FL, 1967, ISBN 0-8493-0303-6 , Organic Derivatives of Phenols, S. 96th
3. ↑ ^{a b c} data sheet 2-propylphenol from Sigma-Aldrich , accessed on August 8, 2017 ( PDF ).
4. ↑ ^{a b} Data sheet 3-n-Propylphenol from AlfaAesar, accessed on August 8, 2017 ( PDF )(JavaScript required) .
5. ↑ ^{a b c} data sheet 4-propylphenol from Sigma-Aldrich , accessed on August 8, 2017 ( PDF ).