PICOLINES
|
GENERAL
|
alpha-PICOLINE,
beta-PICOLINE, and gamma-PICOLINE. The
three compounds are structural isomers. The names of
the three compounds indicate which of the hydrogens
on the benzene ring portion of the molecule have been
replaced. They are obtained from coal tar or petroleum. Because the boiling points of these three compounds are nearly the
same, a separation of a mixture of the three into its
pure components is impractical. PICOLINES are useful
as solvents and as raw materials for various chemical
products used in the industry of polymers,
textiles, fuels, agrochemicals,
pharmaceuticals and colorants.
|
alpha-PICOLINE
|
beta-PICOLINE
|
gamma-PICOLINE
|
|
|
|
CAS
No. : 109-06-8 2-Methylpyridine
|
CAS
No. : 108-99-6 3-Methylpyridine
|
CAS
No. : 108-89-4 4-Methylpyridine
|
APPLICATION
|
Solvents,
Raw materials for various chemical products used in
the industry of polymers,
textiles, fuels, agrochemicals,
pharmaceuticals and colorants.
|
PHYSICAL
PROPERTY |
PROPERTY
|
a-PICOLINE
|
b-PICOLINE
|
g-PICOLINE
|
Melting
Point |
66.5
- 67.5 C |
18.0
- 19.0 C |
3.0
- 4.0 C
|
Boiling
point (at 760mmHg) |
129
- 130 C |
143
- 144 C
|
144.5
- 145.5 C
|
Specific
Gravity (at 25C) |
0.9393 |
0.952
|
0.9504 |
Refractive
Index nD25 |
1.4990
- 1.5000 |
1.5000
- 1.5010
|
1.5030
- 1.5040 |
|
SPECIFICATION |
PROPERTY
|
a-PICOLINE
|
b-PICOLINE
|
g-PICOLINE
|
Appearance
|
Clear
Liquid to
Pale Yellow Liquid
|
Purity
(by GC)
|
99.0%
min
|
98.0%
min
|
98.0%
min
|
Moisture
|
0.15%
max
|
0.2%
max
|
0.2%
max
|
Color
(Pt-Co Scale)
|
25
|
25
|
-
|
|
SYNONYMS |
alpha-PICOLINE 2-Methylpyridine,
Alpha-methylpyridine, 2-Picoline beta-PICOLINE 3-Picoline,
3-Methylpyridine, beta-methylpyridine gamma-PICOLINE 4-Picoline,
sigma-Picoline, G-Picoline, 4-Methylpyridine
|
COMMENTS |
Packing
: 190kgs in Drum |
GENERAL
DESCRIPTION OF PYRIDINE |
PYRIDINE,
also called azabenzene and azine, is a heterocyclic
aromatic tertiary amine characterized by a six-membered
ring structure composed of five carbon atoms and
a nitrogen which replace one carbon-hydrogen unit
in the benzene ring (C5H5N). The simplest member of the
pyridine family is pyridine itself. It is colorless,
flammable, toxic liquid with a unpleasant odor,
miscible with water and with most organic solvents,
boils
at 115 C. Its aqueous solution is slightly alkaline. Its conjugate acid is called
pyridinium cation, C5H5NH+,
used as a oxidation agent for organic synthesis..
Pyridine is a base with
chemical properties similar to tertiary amines. Nitrogen in the ring system
has an equatorial lone pair of electrons, that does not
participate in the aromatic pi-bond. Its
aqueous solution is slightly alkaline. It is incompatible
and reactive with strong oxidizers and strong acids,
and reacts violently with chlorosulfonic acid, maleic
anhydride, oleum, perchromates, b-propiolactone,
formamide, chromium trioxide, and sulfuric acid.
Liquid pyridine easily evaporates into the air.
If it is released to the air, it may take several
months to years until it breaks down into other
compounds. Usually,
pyridine is derived from coal tar or synthesized
from
other chemicals, mainly acetaldehyde and ammonia. Pyridine compounds
are found in nature. For example, nicotine
from tobacco, ricinine from castor bean, pyridoxine or vitamin B and P products, alkaloids
(such as coniine, piperine and nicotine), and etc.
Some pyridine compounds consumed largely are;
Picoline :
Three structural isomers of methyl pyridines (alpha, beta, gamma-
positions) Lutidine : Six structural isomers of dimethyl pyridines (2,3-,
,24-, 2,5-, 2,6-, 3,4-, 3,5- positions) Collidine : Three structural isomers
of trimethyl pyridines (2,3,5-, 2,3,6-, 2,4,6- positions) Pyrimidine:
Pyridine alteration containing nitrogen atoms at positions 1 and
3 Piperidine: Hexahydropyridine (saturated form) Nicotinic acid:
pyridine-3-carboxylic acid Pyridine and
its derivatives are
very important in industrial field as well as in bio chemistry. Nucleotide consist of either a nitrogenous heterocyclic base (purine or
pyrimidine). Three major pyrimidines in living systems are cytosine, thymine, and uracil.
Pyrimidine and its derivatives are biologically important components of nucleic
acids (DNA, RNA) and coenzymes. Some pyridine system is active in the metabolism in
the body. They can be the parent compound of many drugs,
including the barbiturates.
Pyridine and
its derivatives are used as solvents and starting material for the synthesis of target
compounds such as insecticides, herbicides, medicines, vitamins, food flavorings, feed additives, dyes,
rubber chemicals, explosives, disinfectants, and adhesives. Pyridine is also used as a denaturant for antifreeze mixtures, as a
dyeing assistant in textiles and in fungicides. Compounds not made from pyridine
but containing its ring structure include niacin and pyridoxal; isoniazid,
nicotine, and several other nitrogenous plant products. |
PICOLINE
PRODUCTS
|
Product
|
CAS
RN
|
1-(2'-Hydroxyphenylacetyl)-4-methyl-1,2,3,6-tetrahydropyridine |
24789-84-2 |
1,4-Dihydro-4-imino-1-phenethyl-2-picoline monohydrobromide |
33262-96-3 |
1-Phenethyl-2-picolinium bromide |
10551-21-0 |
2-(2-Chloroethyl)-6-methylpyridine hydrochloride |
17944-62-6 |
2-(3,4,5-Trimethoxybenzamido)-3-picoline |
36845-03-1 |
2-(o-Aminobenzamido)-3-picoline |
36844-99-2 |
2-(p-(Dimethylamino)benzamido)-3-picoline |
36844-94-7 |
2-(p-Aminobenzamido)-3-picoline dihydrochloride |
17710-07-5 |
2-(p-Aminobenzamido)-3-picoline |
17710-06-4 |
2-(p-Aminobenzamido)-4-picoline |
36845-05-3 |
2-(p-Amino-N-methylbenzamido)-3-picoline |
36844-96-9 |
2-(p-Chlorobenzamido)-3-picoline |
36845-02-0 |
2-(p-Methylbenzamido)-3-picoline |
36845-01-9 |
2-(p-Nitrobenzamido)-3-picoline |
17710-04-2 |
2,2'-Bipyridine,
4,4'-dimethyl- |
1134-35-6 |
2-Amino-3-methylpyridine
|
1603-40-3 |
2-Amino-4-picoline
|
695-34-1 |
2-Amino-6-picoline |
1824-81-3 |
2-Benzamido-3-picoline |
23612-46-6 |
2-Formylpyridine
thiosemicarbazone |
3608-75-1 |
2-Methyl-5-ethylpyridine |
104-90-5 |
2-Methyl-5-vinylpyridine
|
140-76-1 |
2-Methylpiperidine
|
109-05-7 |
2-Methylpyridine
|
109-06-8 |
2-Methylpyridine-1-oxide-4-azo-p-dimethylaniline |
7347-46-8 |
2-Methylpyridine-4-azo-p-dimethylaniline |
41287-11-0 |
2-Picoline,
4-((p-(dimethylamino)phenyl)azo)- |
63019-78-3 |
2-Picoline, 5-ethyl-,
1-oxide |
768-44-5 |
2-Picoline-6-amino-4-nitro-1-oxide
|
40314-76-9 |
2-Picoline-N-oxide hydrochloride |
19305-07-8 |
3-(2-Chloroethyl)-2-methylpyridine hydrochloride |
5959-98-8 |
3-(Chloromethyl)pyridine
|
3099-31-8 |
3-Ethyl-2-picoline hydrochloride |
31299-84-0 |
3-Ethyl-4-picoline
|
529-21-5 |
3-Methyl-4-aminopyridine
|
1990-90-5 |
3-Methyl-4-nitropyridine
1-oxide |
1074-98-2 |
3-Methylpiperidine |
626-56-2 |
3-Methylpyridine
|
108-99-6 |
3-Methylpyridine-1-oxide-4-azo-p-dimethylaniline |
31932-35-1 |
3-Picoline-4-carboxaldehyde,
thiosemicarbazone |
3608-78-4 |
3-Picoline-N-oxide |
1003-73-2 |
4-((4-(Dimethylamino)-m-tolyl)azo)-2-picoline 1-oxide |
7347-47-9 |
4-((4-(Dimethylamino)-m-tolyl)azo)-3-picoline 1-oxide |
19456-74-7 |
4-((4-(Dimethylamino)-o-tolyl)azo)-2-picoline 1-oxide |
7347-48-0 |
4-((4-(Dimethylamino)-o-tolyl)azo)-3-picoline 1-oxide |
19471-28-4 |
4-(alpha-(2-(Dimethylamino)ethyl)benzyl)-2-picoline |
101602-45-3 |
4-(p-aminobenzamido)-3-picoline |
36855-65-9 |
4-(p-Chloro-alpha-(2-(dimethylamino)ethyl)benzyl)-2-picoline |
101581-59-3 |
4-(p-Nitrobenzamido)-3-picoline |
36855-64-8 |
4,6-Bis((3-chloro-3,3-difluoro-2-hydroxy-2-trifluoromethyl)propyl)-2-picoline |
102206-52-0 |
4-Benzylpicoline |
7300-29-0 |
4-Ethyl-2-picoline
|
536-88-9 |
4-Methyl-2-aminopyridine-palladium
chloride |
77839-67-9 |
4-Methyl-2-pyridinamine hydrochloride |
32654-41-4 |
4-Methyl-N-(phenylmethyl)-2-pyridinamine |
13021-71-1 |
4-Methylpyridine |
108-89-4 |
4-Methylpyridine
|
108-89-4 |
4-Nitro-3-picoline |
1678-53-1 |
4-Picoline-N-oxide
|
1003-67-4
|
5-(3-Piperidino-1-propynyl)-2-picoline |
73771-10-5 |
5-Acetyl-2-picoline |
36357-38-7 |
6-(p-aminobenzamido)-2-picoline |
36845-08-6 |
6-(p-Aminobenzamido)-3-picoline |
17710-08-6 |
6-(p-Nitrobenzamido)-2-picoline |
37586-00-8 |
6,6'-Dimethyl-2,2'-bipyridyl |
4411-80-7 |
6-Amino-beta-picoline |
1603-41-4 |
6-Chloro-2-picoline |
18368-63-3 |
6-Iodo-2-picolin-5-ol |
23003-30-7 |
6-Methoxy-3-picoline |
13472-56-5 |
6-Methylpyridine-2-carboxylic
acid |
934-60-1 |
Dichlorotetrakis(3-picoline)rhodium(1+) chloride |
97348-99-7 |
Hexachloro-2-picoline |
76840-11-4 |
Methylpyridine
|
1333-41-1 |
Picoline, 1-oxide
(6CI,7CI) |
51279-53-9 |
Poly(N-ethyl-N-(2-chloroethyl)-p-aminobenzaldehyde, gamma-picoline) |
71566-74-0 |
Polychlorinated picoline |
70024-85-0 |
Pyridine,
2,3,4,5-tetrachloro-6-(trichloromethyl)- |
1134-04-9 |
Pyridine, 2-methyl-,
1-oxide |
931-19-1 |
Pyridoxine
|
65-23-6 |
Pyridoxine hydrochloride |
58-56-0 |
Pyridoxine tripalmitate
|
4372-46-7 |
Pyroxychlor |
7159-34-4 |
S-2-((5-(4-Methyl-2-pyridyloxy)pentyl)amino)ethyl hydrogen thiosulfate |
41287-10-9 |
trans-Dichlorotetrakis(3-picoline)rhodium chloride |
22933-76-2 |
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