Butan-1,2,3,4-tetracarbonsure

Bezeichnung:Butan-1,2,3,4-tetracarbonsure

CAS-Nr1703-58-8

Englisch Name:1,2,3,4-Butanetetracarboxylic acid

CBNumberCB5251171

SummenformelC8H10O8

Molgewicht234.16

MOL-Datei1703-58-8.mol

Synonyma

Butan-1,2,3,4-tetracarbonsure

Butan-1,2,3,4-tetracarbonsure physikalisch-chemischer Eigenschaften

Schmelzpunkt	193-197 °C
Siedepunkt	296.47°C (rough estimate)
Dichte	1.5040 (rough estimate)
Dampfdruck	0Pa at 25℃
Brechungsindex	1.5800 (estimate)
storage temp.	Sealed in dry,Room Temperature
Löslichkeit	118g/l
Aggregatzustand	Crystalline Powder
pka	pK1: 3.43;pK2: 4.58;pK3: 5.85;pK4: 7.16 (25°C)
Farbe	White
Wasserlöslichkeit	>=10 g/100 mL at 19 ºC
BRN	1729167
InChIKey	GGAUUQHSCNMCAU-UHFFFAOYSA-N
LogP	-1.41 at 25℃
CAS Datenbank	1703-58-8(CAS DataBase Reference)
EPA chemische Informationen	1,2,3,4-Butanetetracarboxylic acid (1703-58-8)

Sicherheit

Kennzeichnung gefährlicher	Xn
R-Sätze:	22-36-36/37/38
S-Sätze:	26-37/39
RIDADR	3261
WGK Germany	3
RTECS-Nr.	EK6100000
TSCA	Yes
HS Code	29171990
Toxizität	LD50 orally in Rabbit: 1720 mg/kg

Gefahreninformationscode (GHS)

1,2,3,4-Butanetetracarboxylic acid Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:
R22:Gesundheitsschädlich beim Verschlucken.
R36:Reizt die Augen.
R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.
S-Sätze Betriebsanweisung:
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S37/39:Bei der Arbeit geeignete Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
Chemische Eigenschaften
White leaf-shaped or needle-shaped crystals. melting point 236-237℃ for dextrorotatory-levorotatory type, 189℃ for endocyclic type. Solubility of the product in water (g/100g water): 30℃, 18.5; 50℃, 45.5; 70℃, 81.8. Soluble in ethanol. There is almost no hygroscopicity, and the purity does not decrease when left for more than two years.
Verwenden
1,2,3,4-Butanetetracarboxylic acid (BTCA) is a perfect formaldehyde-free durable press (DP) finishing agent. It has high activity of reaction and no irritant odor.It is used as cotton, hemp, silk and other cellulosic fibers, anti-wrinkle and anti-shrink agent, with the finishing agent for fabric finishing, can improve the shaping effect and the fabric does not contain formaldehyde.
BTCA, catalyzed by sodium hypophosphite (SHP), brings good antiwrinkle property to cotton fabrics and causes significant strength losses due to cross-linking and acidic degradation of cellulose simultaneously.
Verwenden
1,2,3,4-Butanetetracarboxylic acid is used as a cross linking agent to prepare cotton cellulose in order to improve anti-prilling and flame retardant properties. It is used as a spacer in the cross-linking of titania nanoparticles to cotton. Further, it is used as a nonformaldehyde durable press finishing agent.
synthetische
1,2,3,4-butanetetracarboxylic acid is obtained by oxidation of tetrahydrophthalic anhydride.
1,2,3,4-butanetetracarboxylic acid is prepared by oxidative cleavage of tetraphthalic acid or anhydride by oxidation with ozone-containing gas, followed by oxygen-containing gas, with the mixture then being heated with a peroxide, e.g. H2 O2, at 100° C. to produce the butanetetracarboxylic acid.
Process for preparing 1,2,3,4-butanetetracarboxylic acid
Allgemeine Beschreibung
Leaflets (from water) or white powder.
Air & Water Reaktionen
Soluble in water.
Reaktivität anzeigen
1,2,3,4-Butanetetracarboxylic acid is a carboxylic acid. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water; those with more than six carbons are slightly soluble in water. Soluble carboxylic acid dissociate to an extent in water to yield hydrogen ions. The pH of solutions of carboxylic acids is therefore less than 7.0. Many insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in 1,2,3,4-Butanetetracarboxylic acid to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions
Health Hazard
ACUTE/CHRONIC HAZARDS: When heated to decomposition 1,2,3,4-Butanetetracarboxylic acid emits acrid smoke and irritating fumes.
Brandgefahr
Flash point data for 1,2,3,4-Butanetetracarboxylic acid are not available; however, 1,2,3,4-Butanetetracarboxylic acid is probably combustible.
Flammability and Explosibility
Not classified

1,2,3,4-Butanetetracarboxylic acid Upstream-Materialien And Downstream Produkte

Butan-1,2,3,4-tetracarbonsure Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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