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3-Hydroxybutyraldehyd

ALDOL Struktur
107-89-1
CAS-Nr.
107-89-1
Bezeichnung:
3-Hydroxybutyraldehyd
Englisch Name:
ALDOL
Synonyma:
ALDOL;ACETALDOL;Oxybutanal;3-Butanolal;107-89-1 ALDOL;3-Hydroxybutanal;3-hydroxy-butana;Aldol(Technical);3-hydroxy-Butanal;6-HYDROXY-BUTANAL
CBNumber:
CB8756026
Summenformel:
C4H8O2
Molgewicht:
88.11
MOL-Datei:
107-89-1.mol

3-Hydroxybutyraldehyd Eigenschaften

Schmelzpunkt:
<25 °C
Siedepunkt:
bp20 83°
Dichte
d16 1.109
Dampfdichte
3.04
Brechungsindex
1.4238
Flammpunkt:
150°F (OC)
pka
14.50±0.20(Predicted)
Farbe
Clear, white-to-yellow syrupy liquid
EPA chemische Informationen
Acetaldol (107-89-1)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Kennzeichnung gef?hrlicher T
R-S?tze: 24-36
S-S?tze: 26-28-36/37-45
RIDADR  2839
HazardClass  6.1(a)
PackingGroup  II
Giftige Stoffe Daten 107-89-1(Hazardous Substances Data)
Toxizit?t LD50 orally in rats: 2.18 g/kg (Smyth)
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H310 Lebensgefahr bei Hautkontakt. Acute toxicity,dermal Category 1, 2 Achtung GHS hazard pictogramssrc="/GHS06.jpg" width="20" height="20" /> P262, P264, P270, P280, P302+P350,P310, P322, P361, P363, P405, P501
H319 Verursacht schwere Augenreizung. Schwere Augenreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P305+P351+P338,P337+P313P
Sicherheit
P262 Nicht in die Augen, auf die Haut oder auf die Kleidung gelangen lassen.
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P270 Bei Gebrauch nicht essen, trinken oder rauchen.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P302+P350 BEI KONTAKT MIT DER HAUT: Behutsam mit viel Wasser und Seife waschen.
P305+P351+P338 BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach M?glichkeit entfernen. Weiter spülen.
P310 Sofort GIFTINFORMATIONSZENTRUM/Arzt/ anrufen.
P322 Gezielte Ma?nahmen
P361 Alle kontaminierten Kleidungsstücke sofort ausziehen.
P363 Kontaminierte Kleidung vor erneutem Tragen waschen.
P405 Unter Verschluss aufbewahren.
P501 Inhalt/Beh?lter ... (Entsorgungsvorschriften vom Hersteller anzugeben) zuführen.

3-Hydroxybutyraldehyd Chemische Eigenschaften,Einsatz,Produktion Methoden

Chemische Eigenschaften

Aldol is a flammable, colorless to pale yellow, syrupy liquid. Pungent odor

Verwenden

Acetaldol is manufactured by condensing of acetaldehyde in aqueous NaOH and is used to produce rubber vulcanizers, accelerators and age retardants, perfumes, and in ore flotation. It is a hypnotic and sedative.

Allgemeine Beschreibung

A clear white to yellow syrupy liquid. Denser than water. Flash point 150°F. Contact may irritate skin and eyes. Moderately toxic by ingestion, inhalation and skin absorption.

Air & Water Reaktionen

Soluble in water.

Reaktivit?t anzeigen

An aldehyde and alcohol. Aldehydes are frequently involved in self-condensation or polymerization reactions. These reactions are exothermic; they are often catalyzed by acid. Aldehydes are readily oxidized to give carboxylic acids. Flammable and/or toxic gases are generated by the combination of aldehydes with azo, diazo compounds, dithiocarbamates, nitrides, and strong reducing agents. Aldehydes can react with air to give first peroxo acids, and ultimately carboxylic acids. These autoxidation reactions are activated by light, catalyzed by salts of transition metals, and are autocatalytic (catalyzed by the products of the reaction). The addition of stabilizers (antioxidants) to shipments of aldehydes retards autoxidation. Flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents. They react with oxoacids and carboxylic acids to form esters plus water. Oxidizing agents convert them to aldehydes or ketones. Alcohols exhibit both weak acid and weak base behavior. They may initiate the polymerization of isocyanates and epoxides.

Health Hazard

TOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.

Brandgefahr

Combustible material: may burn but does not ignite readily. When heated, vapors may form explosive mixtures with air: indoors, outdoors and sewers explosion hazards. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form.

Sicherheitsprofil

Poison via skin contact. Moderately toxic by ingestion. A skin and eye irritant. A flammable liquid and fire hazard when exposed to heat or flame; emits crotonaldehyde and water when heated. See CROTONALDEHYDE. Can react with oxidtzing materials.

m?gliche Exposition

Aldol is used as a solvent and to manufacture rubber accelerators, perfumes; in fungicides; and in engraving, cadmium plating

Versand/Shipping

UN2839 Aldol, Hazard Class: 6.1; Labels: 6.1Poison Inhalation Hazard

l?uterung methode

An ethereal solution of aldol is washed with a saturated aqueous solution of NaHCO3, then with water. The non-aqueous layer is dried with anhydrous CaCl2 and distilled immediately before use. The fraction, b 80-81o/20mm, is collected as a thick liquid which decomposes at 85o/atm. It is a sedative and a hypnotic but is used in perfumery. [Mason et al. J Am Chem Soc 76 2255 1954]. [Beilstein 1 H 824, 1 I 419, 1 II 868, 1 III 3195, 1 IV 3984.]

Inkompatibilit?ten

Danger! May be subject to spontaneous polymerization. Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires orexplosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. Contact with metals may evolve flammable hydrogen gas. Heat above 83 C causes the formation of crotonaldehyde vapor (which may cause explosion) and water.

Waste disposal

Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed.

3-Hydroxybutyraldehyd Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


3-Hydroxybutyraldehyd Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 31)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Hebei Yanxi Chemical Co., Ltd.
+8617531190177
peter@yan-xi.com China 5857 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512
info@tianfuchem.com China 21634 55
Hubei xin bonus chemical co. LTD
86-13657291602
linda@hubeijusheng.com CHINA 22963 58
Zhuoer Chemical Co., Ltd
02120970332; +8613524231522
sales@zhuoerchem.com China 2904 58
Shaanxi Didu New Materials Co. Ltd
+86-89586680 +86-13289823923
1026@dideu.com China 8670 58
Mainchem Co., Ltd. +86-0592-6210733
sale@mainchem.com China 32343 55
LGM Pharma 1-(800)-881-8210
inquiries@lgmpharma.com United States 2123 70
China Langchem Inc. 0086-21-58956006
China 7811 57
Hangzhou Sage Chemical Co., Ltd. +86057186818502 13588463833
info@sagechem.com China 10266 58
Shanghai Topbiochem Technology Co., Ltd +86-21-60341587
sales@topbiochem.com China 6175 58

107-89-1(3-Hydroxybutyraldehyd)Verwandte Suche:


  • 3-Butanolal
  • 3-hydroxy-butana
  • 3-Hydroxybutanal
  • 3-hydroxy-Butanal
  • 3-hydroxy-butyraldehyd
  • beta-Hydroxybutyraldehyde
  • Butanal, 3-hydroxy-
  • Butanal,3-hydroxy-
  • Butyraldehyde, 3-hydroxy-
  • Oxybutanal
  • Oxybutyric aldehyde
  • oxybutyricaldehyde
  • ACETALDOL
  • ALDOL
  • 3-HYDROXYBUTYRALDEHYDE
  • 6-HYDROXY-BUTANAL
  • β-Hydroxybutyraldehyde
  • Aldol (Acetaldol)
  • Aldol Tech. Grade
  • Aldol(Technical)
  • Aldol DISCONTINUED. Can be prepared (and used without isolation) from H824630. Please see Journal of Organic Chemistry, 1988, 53, 4175-4181.
  • 107-89-1 ALDOL
  • 107-89-1
  • CH3CHOHCH2CHO
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