|
PHTHALIC
ANHYDRIDE
|
|
PRODUCT
IDENTIFICATION
|
| CAS
NO. |
85-44-9 |

|
| EINECS
NO. |
201-607-5 |
| FORMULA |
C6H4(CO)2O |
| MOL
WT. |
148.12 |
|
H.S.
CODE
|
2917.35 |
| TOXICITY |
Oral rat LD50:
1530 mg/kg |
| SYNONYMS |
1,3-Isobenzofuranidone;
1,3-Dioxophthalan; Phthalandione; |
| 1,3 Phthalandione; 1,2-Benzenedicarboxylic acid anhydride; Phthalic acid anhydride;
1,2-Benzenedicarboxylic anhydride; 1,3-dihydro-1,3-dioxoisobenzofuran;
|
| DERIVATION |
|
|
CLASSIFICATION
|
CARBOXYLIC
ACID ANHYDRIDES /
|
|
GENERAL
DESCRIPTION
|
|
Phthalic anhydride, the anhydride form of phthalic acid , is produced by the
oxidation of orthoxylene and naphthalene. Its wide application is based on the
ortho related carboxylic acid groups as their dehydration is highly reactive
with broad processing conditions to produce various downstream products. It is
used to make simple esters widely used as plasticizers. It is used as in making
unsaturated polyester resins, alkyd resins, polyester polyols, dyes and
pigments, halogenated anhydrides, polyetherimide resins, isatoic anhydride and
insect repellents.
Anhydride is a
compound formed by the abstraction of a molecule of water,
H2O, from a substance.
The term acid anhydride is restricted sometime to the anhydride formed
especially from an acid by dehydration or one that revert to the original
substance upon hydration. In case of bimolecular, it can be composed of two
molecules of the corresponding acid. The term mixed anhydride is an acid
anhydride composed of two different acids. Examples are adenosine triphosphate
or an aminoacyl adenylate. The anhydrides of bases are oxides.
Anhydrides of
inorganic acids are usually oxides of nonmetallic elements. Carbon dioxide
(CO2) is the anhydride of
carbonic acid, dinitrogen pentoxide (N2O5) is the anhydride of
nitric acid, sodium oxide is an anhydride of sodium hydroxide,
phosphorus pentoxide (P2O5) is the anhydride of
phosphoric acid, and sulfur trioxide (SO3) is the anhydride of
sulfuric acid. An acid anhydride forms
an acid; a base anhydride forms a base.
Sulfur trioxide (acid anhydride) reacts with water to form sulfuric acid (an
acid product). Calcium oxide
(an base anhydride) reacts with water to form calcium hydroxide (a base product).
Organic anhydrides contain the carbonyl group (CO).
Organic anhydrides are formed by the condensation of original acids. Lactone, an
internal cyclic monoester, is an anhydride derived from the hydroxyl and
carboxyl radicals. In organic chemistry, most
anhydride compounds are
derived from corresponding carboxylic acids. Carboxylic anhydrides, general formula (RCO)2O, are
the dehydration product of two carboxylic acid molecules. The name of carboxylic
anhydride is
given first from the original acid, followed by the separate word "anhydride".
[CH3(CH2)2CO]2O is butanoic
anhydride, CH3COOCOCH2CH3 is
ethanoic propanoic anhydride (or
acetic propionic anhydride). Anhydrides are more reactive than the parent acids. Anhydrides are typically not
target molecules, but rather they are used as intermediates for the synthesis of
other organic members such as esters and amides for the industrial applications
include dyes, pharmaceuticals, pesticides, plastics, fibers, curing agents,
plasticizers and many others. The reactivity
of carboxylic acid derivatives are in order of acyl halides > anhydrides >> esters ¡Ö acids >> amides.
Anhydrides react with alcohols to form esters; acetic anhydride [(CH3CO)2O] reacts with
ethanol (C2H5OH)
to form ethyl acetate (CH3COOC2H5)
used as a common solvent. Anhydrides also react with ammonia and
primary or secondary amines to form amides. Anhydrides react with water to form their corresponding acids.
|
|
PHYSICAL
AND CHEMICAL PROPERTIES
|
| PHYSICAL
STATE |
white crystalic flakes |
| MELTING
POINT |
130
- 131 C |
| BOILING
POINT |
284
C |
| SPECIFIC
GRAVITY |
1.53 |
| SOLUBILITY
IN WATER |
6 g/l (Decomposes
to phthalic acid) |
|
SOLUBILITY
|
soluble in alcohol,
slightly soluble in ether |
| pH |
|
| VAPOR
DENSITY |
5.1 |
|
AUTOIGNITION
|
570
C
|
|
NFPA
RATINGS
|
Health: 2; Flammability: 1; Reactivity: 0 |
|
REFRACTIVE
INDEX
|
|
| FLASH
POINT |
|
| STABILITY |
Stable
under ordinary conditions. |
|
APPLICATIONS
|
|
Plasticizers,
unsaturated polyester resins, alkyd
resins, polyester polyols, dyes and
pigments, halogenated anhydrides, polyetherimide resins, and isatoic anhydride.
|
| SALES
SPECIFICATION |
|
|
|
MOLTEN |
SOLDID |
|
APPEARANCE |
|
Clear |
White flakes |
|
PURITY(%) |
L.C
|
Min. 99.85 |
Min. 99.85 |
|
COLOUR INDEX |
D3366
|
Max. 15 |
Max. 20 |
|
HAZEN |
D3366
|
Max. 25 |
Max. 40 |
|
MELTING
POINT |
D1493
|
Min. 130
C |
Min. 130
C |
|
|
TRANSPORTATION
|
| PACKING |
25kgs
in bag |
| HAZARD
CLASS |
8
(Packing Group: III) |
| UN
NO. |
2214
|
| OTHER
INFORMATION |
|
Hazard Symbols: XI, C, Risk Phrases: 34-36/37/38 , Safety
Phrases: |
|
GENERAL
DESCRIPTION OF PHTHALIC ACID
|
|
Phthalic Acid, also called Benzenedicarboxylic Acid with formula C6H4(COOH)2, is
the name of any of three isomers. The ortho form (1,2-benzenecarboxylic acid)
is called simply phthalic acid. It is a white crystals decomposing at 191°C and
slightly soluble in water and ether. This compound is mainly produced and
marketed in the form of its anhydride produced by the oxidation of orthoxylene
and naphthalene. Its wide application is based on the ortho related carboxylic
acid groups as their dehydration is highly reactive with broad processing
conditions to produce various downstream products. It is used to make simple
esters widely used as plasticizers. It is used as in making unsaturated
polyester resins, alkyd resins, polyester polyols, dyes and pigments,
halogenated anhydrides, polyetherimide resins, isatoic anhydride and insect
repellents. The meta form is isophthalic acid (1,3-benzenecarboxylic acid). It
is a white crystals subliming at 345°C slightly soluble in water, alcohol and
acetic acid (insoluble in benzene). It is obtained by oxidizing meta-xylene with
chromic acid, or by fusing potassium meta-sulphobenzoate, or meta-brombenzoate
with potassium formate. IPA has excellent performance characteristics in coatings including excellent
hardness, corrosion and stain resistance, hydrolytic stability of coatings and
gel coats, excellent thermal stability and low resin color. It is a key ingredient in FRP markets for such products
as marine, automotive, and corrosion resistant pipes and tanks. Polyesters
containing isophthalic acid are also used extensively in industrial coatings
applications for home appliances, automobiles, aluminum siding, and metal office
furniture. It used as an intermediate for polyesters, polyurethane resins,
plasticizers. The para form, known as terephthalic acid (1,4-benzenecarboxylic
acid) is a combustible white powder insoluble in water, alcohol and ether;
(soluble in alkalies), sublimes at 300°C. It can be produced by oxidizing
caraway oil, a mixture of cymene and cuminol or by oxidizing para-diderivatives
of benzene with chromic acid. TPA has been used mainly as a raw material of
polyester fiber but lately it has been exploited for various uses such as
non-fiber field, PET-bottle, PET-film and engineering plastics and as poultry
feed additives. Phthalic acid derivatives are also widely used to make dyes,
medicine, and synthetic perfumes, pesticides, and other chemical compounds. |
|
|
|