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INDOLE-3-PYRUVIC ACID | ||
PRODUCT IDENTIFICATION |
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CAS NO | 392-12-1 | |
EINECS NO. |
206-874-1 | |
FORMULA | C11H9NO3 | |
MOL WT. | 203.20 | |
H.S. CODE |
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TOXICITY |
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SYNONYMS | 3-(3-Indolyl)-2-oxopropanoic acid; | |
alpha-Oxo-1H-indole-3-propanoic acid; Indolepyruvate; 3-Indolylpyruvic acid; | ||
SMILES |
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CLASSIFICATION |
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PHYSICAL AND CHEMICAL PROPERTIES |
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PHYSICAL STATE | off white crystals | |
MELTING POINT | 208 -215 C | |
BOILING POINT |
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SPECIFIC GRAVITY |
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SOLUBILITY IN WATER | ||
SOLVENT SOLUBILITY |
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pH | ||
VAPOR DENSITY |
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REFRACTIVE INDEX |
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AUTOIGNITION |
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NFPA RATINGS | ||
FLASH POINT |
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STABILITY |
Stable under ordinary conditions. Light/air sensitive. | |
APPLICATIONS |
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Indole, benzopyrrole, is a yellow crystalline powder with unpleasant aroma. It
has the pyrrole ring (five-membered unsaturated ring structure composed of four
carbon atoms and one nitrogen atom) which is fused to benzene ring. There are
tautomerer called indolenine (unsubstituted 3H-indole) and structural isomer,
isoindole. But they are unstable. Indole occurs in some plants or in coal tar,
and is formed in the intestine during putrefaction and by certain cultures of
bacteria. it is commercially synthesized from phenylhydrazine and pyruvic acid. Indole structure is a
motif in nature. Prominent examples include tryptophan (aromatic side chain amino acid), serotonin
(neurotransmitter), auxin (plant growth hormone), and indigo (plant colorant).
One more interesting point is all these compounds have functional branches at
3
position.
Indole is used in perfumery and in preparing tryptophan, one of the 20 amino acids
commonly found in animal proteins. It has important application in the industry
of plant growth. It is used to prepare indoleacetic acid (auxin) and other
plant growth substances which help the development of roots in plant. It is used
to make selective herbicides. Indole and its derivatives are widely used in
making perfumes, dyes, agrochemicals and medicines.
Pyruvic acid is a low mole weight alpha keto acid (ketone along with carboxylic acid). It contains a ketone bond on the carbon atom next to the acid group. If the ketone is on the second carbon next to the acid group, it is called beta-keto acid. Pyruvic acid is a liquid with acetic-acid smell; melting point 11 - 12 C; solube in water. It occurs naturally as an intermediate product in carbohydrate and protein metabolism in the body. The six-carbon glucose molecule is broken down to two molecules of pyruvic acid in aerobic condition as the main input for Krebs cycle, whereas to two molecules of lactic acid (alpha hydroxy acid) in anaerobic condition. Krebs cycle (also called citric acid cycle; tricarboxylic acid cycle) is a sequent process of enzymatic reaction which a two-carbon acetyl unit is oxidized to carbon dioxide and water to provide energy in the form of high-energy phosphate bonds. Pyruvic acid is used commercially to produce its salts and esters (pyruvates) used as dietary supplements for the effect of enhancing weight loss. Pyruvic acid is used for the synthesis of amino acids (alanine, tyrosine, phenylalanine, and tryptophan) and used in biochemical research. Its derivatives are used in making food additives and flavoring agents. |
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SALES SPECIFICATION | ||
APPEARANCE |
off white crystals | |
ASSAY |
98.0% min |
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MELTING POINT | 208 -215 C | |
TRANSPORTATION | ||
PACKING |
25kgs in fiber drum | |
HAZARD CLASS | ||
UN NO. | ||
OTHER INFORMATION | ||
Hazard Symbols: XN, Risk Phrases: 36/37/38, Safety Phrase: 22-24/25 |
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GENERAL DESCRIPTION OF PLANT HORMONE |
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Auxin is one of
five (or more) major plant hormones (Auxin, Cytokinins, Gibberellins, Ethylene
and Abscisic acid) which affect numerous plant growth processes functions
including cell division and elongation, autumnal loss of leaves, and the
formation of buds, roots, flowers, and fruit. Auxin action is inhibited by
light which is an important role of the growth of stems toward light
(phototropism), against the force of gravity (geotropism) and positively
hydrotropic (moisture-seeking). The cells exposed to light don't grow as quickly
as those on the shaded side, and thus the plant grows toward the light source.
Auxins usually have a ring system with at least one double bond and attached by
a side-chain that terminates in a carboxyl group. Indole acetic acid is the
exact structure of Auxin activity. Parent compounds of auxin action are;
Cytokinin is a N6-substituted adenines acting as phytohormones such as kinetin, zeatin, 6-isopentenyladenine, benzyl adenine. The principal functions are stimulate cell division in concert with auxin (cytokinesis) and influence the pathway of tissue differentiation (organogenesis). 6-Benzylaminopurine is the first generation synthetic cytokinin which elicits plant growth and development responses setting blossoms and stimulating fruit richness by stimulating cell division. Active cytokinin ingredients include:
Other Plant Growth Regulators include:
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PRICE | ||
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