| CAS
NO. |
112-05-0
|
|
| EINECS
NO. |
203-931-2 |
| FORMULA |
CH3(CH2)7COOH |
| MOL
WT. |
158.24 |
| H.S.
CODE |
2915.90 |
|
TOXICITY
|
Oral
rat LD50: >5 gm/kg |
| SYNONYMS |
1-Octanecarboxylic
acid; n-Pelargonic
Acid; |
| Nonanoic
Acid; 1-octanecarboxylic Acid; Nonylic Acid; Acide Nonylique
Normal; Acide Pelargonique; Hexacid C-9; Octane-1-carboxylic
Acid; Pelargic Acid; Pelargon (Russian); |
|
PRICE |
U$50/kg CFR by sea
for 100kgs
U$130/kg CFR by air for 10kgs subject to Hazardous Material Fee
|
|
CLASSIFICATION
|
|
|
PHYSICAL
AND CHEMICAL PROPERTIES
|
| PHYSICAL
STATE |
clear
to yellowish oily liquid
|
| MELTING
POINT |
11
C |
| BOILING
POINT |
253
C |
| SPECIFIC
GRAVITY |
0.907 |
| SOLUBILITY
IN WATER |
Insoluble |
| pH |
|
| VAPOR
DENSITY |
5.45 |
| AUTOIGNITION
|
405
C
|
| NFPA
RATINGS |
Health:
3 Flammability: 1 Reactivity: 0 |
|
REFRACTIVE
INDEX
|
1.4322 |
| FLASH
POINT |
114
C
|
| STABILITY |
Stable
under ordinary conditions |
|
DESCRIPTION
AND APPLICATIONS
|
|
Pelargonic
acid is a clear to yellowish oily liquid. It is insoluble
in water but soluble in ether, alcohol and organic solvents. The molecules of most natural fatty acids have an even number of carbon chains
due to the linkage together by ester units. Analogous compounds of odd numbers
carbon chain fatty acids are supplemented synthetically. Pelargonic
acid, C-9 odd numbers
carbon chain fatty acid, is relatively high cost fatty acid.
Pelargonic
acid can
be prepared by ozonolysis which uses ozone is to
cleave the alkene bonds. Eexample of ozonolysis in commerce is the
production of odd carbon number carboxylic acids such as azelaic acid and
pelargonic acid and simple carboxylic acids such as formic acid and oxalic acid.
Pelargonic
acid forms esters with alcohols to
be used as plasticizers and lubricating oils.
It is used in modifying alkyd resins to prevent discolor
and to keep flexibility and resistance to aging since
saturated pelargonic acid will not be oxidized. Metallic
soaps (barium and cadmium) and other inorganic salts used as a stabilizer. It is
also used as a chemical intermediate for synthetic flavors,
cosmetics, pharmaceuticals and corrosion inhibitors. It
is known that C8 - C12 straight and saturated chain
fatty acids are capable of removing the waxy cuticle of the broadleaf or weed,
resulting in causing the tissue
death. They are used as active ingredient of environment friendly and
quick effect
herbicides. Pelargonic
acid is the strongest one.
|
| SALES
SPECIFICATION |
|
APPEARANCE
|
clear
to yellowish oily liquid
|
| CONTENT
OF C9 ACIDS |
98.5%
min
|
|
2-METHYL
OCTANOIC ACID
|
2.5%
max
|
|
WATER
|
0.1%
max
|
|
IODINE
VALUE
|
0.6
max
|
| COLOR |
25
max(Pt/Co scale)
|
| TRANSPORTATION |
| PACKING |
180kgs
in drum |
| HAZARD
CLASS |
Not
regulated |
| UN
NO. |
|
| PRICE
INDICATION |
| USD38.00/kg CFR
by sea
for the quantity 180kgs shipment. |
| GENERAL
DESCRIPTION OF CARBOXYLIC ACID |
Carboxylic acid is an organic compound whose molecules contain carboxyl group
and have the condensed chemical formula R-C(=O)-OH in which a carbon atom is
bonded to an oxygen atom by a double bond and to a hydroxyl group by a single
bond), where R is a hydrogen atom, an alkyl group, or an aryl group. Carboxylic
acids can be synthesized if aldehyde is oxidized. Aldehyde can be obtained by
oxidation of primary alcohol. Accordingly, carboxylic acid can be obtained by
complete oxidation of primary alcohol. A variety of Carboxylic acids are
abundant in nature and many carboxylic acids have their own trivial names.
Examples are shown in table. In substitutive nomenclature, their names are
formed by adding -oic acid' as the suffix to the name of the parent compound.
The first character of carboxylic acid is acidity due to dissociation into H+
cations and RCOO- anions in aqueous solution. The two oxygen atoms are
electronegatively charged and the hydrogen of a carboxyl group can be easily
removed. The presence of electronegative groups next to the carboxylic group
increases the acidity. For example, trichloroacetic acid is a stronger acid than
acetic acid. Carboxylic acid is useful as a parent material to prepare many
chemical derivatives due to the weak acidity of the hydroxyl hydrogen or due to
the difference in electronegativity between carbon and oxygen. The easy
dissociation of the hydroxyl oxygen-hydrogen provide reactions to form an ester
with an alcohol and to form a water-soluble salt with an alkali. Almost infinite
esters are formed through condensation reaction called esterification between
carboxylic acid and alcohol, which produces water. The second
reaction theory is the addition of electrons to the electron-deficient carbon
atom of the carboxyl group. One more theory is decarboxylation (removal of
carbon dioxide form carboxyl group). Carboxylic acids are used to synthesize
acyl halides and acid anhydrides which are generally not target compounds. They
are used as intermediates for the synthesis esters and amides, important
derivatives from carboxylic acid in biochemistry as well as in industrial
fields. There are almost
infinite esters obtained from carboxylic
acids. Esters
are formed by removal of water from an acid and an alcohol. Carboxylic acid
esters are used as in a variety of direct and indirect applications. Lower chain
esters are used as flavouring base materials, plasticizers, solvent carriers and
coupling agents. Higher chain compounds are used as components in metalworking
fluids, surfactants, lubricants, detergents, oiling agents, emulsifiers, wetting
agents textile treatments and emollients, They are also used as intermediates
for the manufacture of a variety of target compounds. The almost infinite esters
provide a wide range of viscosity, specific gravity, vapor pressure, boiling
point, and other physical and chemical properties for the proper application
selections. Amides
are formed from the reaction of a carboxylic acids with an amine.
Carboxylic
acid's reaction to link amino acids is wide in nature to form proteins (amide), the
principal constituents of the protoplasm of all cells. Polyamide is a polymer
containing repeated amide groups such as various kinds of nylon and
polyacrylamides. Carboxylic acid
are in our lives.
|
ALIPHATIC CARBOXYLIC ACIDS |
|
COMMON
NAME
| SYSTEMATIC NAME |
CAS
RN
| FORMULA |
MELTING
POINT
|
| Formic Acid
| Methanoic acid |
64-18-6 | HCOOH | 8.5
C |
| Acetic Acid | Ethanoic acid | 64-19-7 | CH3COOH |
16.5
C
|
| Carboxyethane | Propionic Acid |
79-09-4 | CH3CH2COOH |
-21.5
C
|
| Butyric Acid | n-Butanoic acid |
107-92-6 | CH3(CH2)2COOH |
-8
C
|
| Valeric Acid | n-Pentanoic Acid |
109-52-4 | CH3(CH2)3COOH |
-19
C
|
| Caproic Acid | n-Hexanoic Acid |
142-62-1 | CH3(CH2)4COOH |
-3
C
|
| Enanthoic Acid | n-Heptanoic acid |
111-14-8 | CH3(CH2)5COOH |
-10.5
C
|
| Caprylic Acid | n-Octanoic Acid |
124-07-2 | CH3(CH2)6COOH |
16
C
|
| alpha-Ethylcaproic Acid | 2-Ethylhexanoic Acid |
149-57-5 | CH3(CH2)3CH(C2H5)COOH |
-59
C
|
| Valproic Acid | 2-Propylpentanoic Acid |
99-66-1 | (CH3CH2CH2)2CHCOOH |
120
C
|
| Pelargonic Acid | n-Nonanoic Acid |
112-05-0 | CH3(CH2)7COOH |
48
C
|
| Capric Acid | n-Decanoic Acid |
334-48-5 | CH3(CH2)8COOH |
31
C
|
|