Hydrazin
Bezeichnung:Hydrazin
CAS-Nr302-01-2
Englisch Name:HYDRAZINE
CBNumberCB7742604
SummenformelH4N2
Molgewicht32.05
MOL-Datei302-01-2.mol
Synonyma
Hydrazin
Diamid
Diamin
Nitrogenhydrid
(wasserfrei)
Hydrazin physikalisch-chemischer Eigenschaften
Schmelzpunkt | 1,4°C |
Siedepunkt | 65 °C |
Dichte | 1.011 g/mL at 25 °C |
Dampfdichte | >1 (vs air) |
Dampfdruck | 5 mm Hg ( 25 °C) |
Brechungsindex | n20/D 1.47(lit.) |
Flammpunkt | −4 °F |
storage temp. | 2-8°C |
Löslichkeit | very soluble in H2O, ethanol,methanol |
pka | pK1 (25°): ~6.05 |
Aggregatzustand | Liquid |
Farbe | Clear colorless |
Geruch (Odor) | Fishy or ammonia-like odor detectable at 3 to 4 ppm (mean = 3.7 ppm) |
Explosionsgrenze | 99.99% |
Wasserlöslichkeit | miscible with H2O and the following alcohols: methyl, ethyl, propyl, isobutyl [MER06] |
Merck | 13,4789 |
BRN | 878137 |
Expositionsgrenzwerte | TLV-TWA (skin) 1 ppm (1.3 mg/m3 ) (MSHA and OSHA), 0.1 ppm (ACGIH). |
Dielectric constant | 52.0(20℃) |
Stabilität | Stability May be an explosion hazard, particularly if heated. Incompatible with sources of ignition, light, shock, strong oxidizing agents, strong acids, metal oxides, nitrous oxide, hydrogen peroxide, most common metals, organic materials, porous materials such as wood, paper, asbestos, soil or rust. Many types of metal may cause rapid d |
LogP | -0.16 at 20℃ |
CAS Datenbank | 302-01-2(CAS DataBase Reference) |
IARC | 2A (Vol. 4, Sup 7, 71, 115) 2018 |
EPA chemische Informationen | Hydrazine (302-01-2) |
Kennzeichnung gefährlicher | T,N,F |
R-Sätze: | 45-23/24/25-34-43-50/53-10-51/53-36/37/38-20/21/22-19-11-36/38 |
S-Sätze: | 53-26-36/37-45-61-60-36/37/39-16 |
RIDADR | UN 3293 6.1/PG 3 |
OEL | Ceiling: 0.03 ppm (0.04 mg/m3) [2-hour] |
WGK Germany | 3 |
RTECS-Nr. | MU7175000 |
F | 10-21 |
Selbstentzündungstemperatur | 24 °C on iron rust surface; 270 °C on glass surface |
HazardClass | 8 |
PackingGroup | I |
HS Code | 28251090 |
Giftige Stoffe Daten | 302-01-2(Hazardous Substances Data) |
Toxizität | LD50 in mice (mg/kg): 57 i.v.; 59 orally (Witkin) |
IDLA | 50 ppm |
Gefahreninformationscode (GHS)
-
Bildanzeige (GHS)
-
Alarmwort
Achtung
-
Gefahrenhinweise
H314:Verursacht schwere Verätzungen der Haut und schwere Augenschäden.
H317:Kann allergische Hautreaktionen verursachen.
H350:Kann Krebs verursachen.
H410:Sehr giftig für Wasserorganismen mit langfristiger Wirkung.
-
Sicherheit
P201:Vor Gebrauch besondere Anweisungen einholen.
P261:Einatmen von Staub vermeiden.
P273:Freisetzung in die Umwelt vermeiden.
P280:Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P305+P351+P338:BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach Möglichkeit entfernen. Weiter spülen.
HYDRAZINE Chemische Eigenschaften,Einsatz,Produktion Methoden
-
ERSCHEINUNGSBILD
FARBLOSE, RAUCHENDE UND HYGROSKOPISCHE FLüSSIGKEIT MIT STECHENDEM GERUCH. -
CHEMISCHE GEFAHREN
Zersetzung unter Bildung von Ammoniakrauchen, Wasserstoff und Stickstoffoxiden. Feuer- und Explosionsgefahr. Starkes Reduktionsmittel. Reagiert sehr heftig mit Oxidationsmitteln. Mittelstarke Base. Reagiert sehr heftig mit vielen Metallen, Metalloxiden und porösen Materialien unter Feuer- und Explosionsgefahr. Luft oder Sauerstoff sind für die Zersetzung nicht erforderlich. -
ARBEITSPLATZGRENZWERTE
TLV: 0.01 ppm (als TWA); Hautresorption; Krebskategorie A3 (bestätigte krebserzeugende Wirkung beim Tier mit unbekannter Bedeutung für den Menschen); (ACGIH 2005).
MAK: Hautresorption; Sensibilisierung der Haut; Krebserzeugend Kategorie 2; (DFG 2005).
-
AUFNAHMEWEGE
Aufnahme in den Körper durch Inhalation der Dämpfe, über die Haut und durch Verschlucken. -
INHALATIONSGEFAHREN
Beim Verdampfen bei 20°C kann sehr schnell eine gesundheitsschädliche Kontamination der Luft eintreten. -
WIRKUNGEN BEI KURZZEITEXPOSITION
WIRKUNGEN BEI KURZZEITEXPOSITION:
Die Substanz verätzt die Augen und die Haut. Der Dampf dieser Substanz verätzt die Atemwege. Inhalation des Dampfes kann zu Lungenödem führen (s. Anm.). Möglich sind Auswirkungen auf Leber, Nieren und Zentralnervensystem. Exposition kann zum Tod führen. Die Auswirkungen treten u.U. verzögert ein. ärztliche Beobachtung notwendig. -
WIRKUNGEN NACH WIEDERHOLTER ODER LANGZEITEXPOSITION
Wiederholter oder andauernder Kontakt kann zu Hautsensibilisierung führen. Möglich sind Auswirkungen auf Leber, Nieren und Zentralnervensystem. Möglicherweise krebserzeugend für den Menschen. -
LECKAGE
Gefahrenbereich verlassen! Fachmann zu Rate ziehen! Ausgelaufene Flüssigkeit in abdichtbaren Behältern sammeln. Reste mit Sand oder inertem Absorptionsmittel aufnehmen und an einen sicheren Ort bringen. NICHT mit Sägemehl oder anderen brennbaren Absorptionsmitteln binden. NICHT in die Umwelt gelangen lassen. Persönliche Schutzausrüstung: Vollschutzanzug mit umgebungsluftunabhängigem Atemschutzgerät. -
R-Sätze Betriebsanweisung:
R45:Kann Krebs erzeugen.
R23/24/25:Giftig beim Einatmen, Verschlucken und Berührung mit der Haut.
R34:Verursacht Verätzungen.
R43:Sensibilisierung durch Hautkontakt möglich.
R50/53:Sehr giftig für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen haben.
R10:Entzündlich.
R51/53:Giftig für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen haben.
R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.
R20/21/22:Gesundheitsschädlich beim Einatmen,Verschlucken und Berührung mit der Haut.
R19:Kann explosionsfähige Peroxide bilden.
R11:Leichtentzündlich. -
S-Sätze Betriebsanweisung:
S53:Exposition vermeiden - vor Gebrauch besondere Anweisungen einholen.
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).
S61:Freisetzung in die Umwelt vermeiden. Besondere Anweisungen einholen/Sicherheitsdatenblatt zu Rate ziehen.
S60:Dieses Produkt und sein Behälter sind als gefährlicher Abfall zu entsorgen.
S36/37/39:Bei der Arbeit geeignete Schutzkleidung,Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen. -
Beschreibung
Hydrazine sulphate, hydrobromide and hydrochloride have been reported to be occupational sensitizers, mainly in soldering flux. -
Chemische Eigenschaften
colourless oily liquid -
Chemische Eigenschaften
HYDRAZINE, colorless, fuming liquid, decomposes when heated above 350 °C at atmospheric pressure into N2 and NH2, also decomposes in presence of a catalyst (e.g., platinum) into N2 and NH3. Hydrazine burns when ignited in air with a violet-colored flame. The compound is soluble in all proportions with H2O and is soluble in alcohol. Hydrazine forms a hydrate with one molecule of H2O. Upon moderate heating or in a vacuum, the hydrate yields hydrazine and H2O. Hydrazine is a base slightly weaker than NH4OH. -
Physikalische Eigenschaften
Colorless, mobile, fuming liquid; ammoniacal odor; density 1.0045 g/mL at25°C; refractive index 1.46044 at 22°C; solidifies at 2°C to a white crystallinesolid; boils at 113.5°C; flash point 52°C; burns with a violet flame; vapor pres-sure 14.4 torr at 25°C; critical temperature 379.85°C; critical pressure 145atm; surface tension 66.67 dyne/cm at 25°C; dielectric constant 51.7 at 25°C;viscosity 0.876 centipoise at 25°C; very soluble in water; forms an azeotropewith water at molar composition of 58.5% hydrazine: 41.5% water (71.48%:28.52% by weight), the azeotrope with water boils at 120.5°C; forms hydrazinehydrate at 1:1 molar concentration in water; soluble in alcohols and other polar solvents; pKa 8.1 at 25°C. -
History
Hydrazine was isolated first as a sulfate salt by Curtius in 1887. Earlier, in1875, Fischer prepared and identified the organic derivatives of hydrazine.Raschig in 1906 prepared hydrazine by hypochlorite oxidation of ammonia.
Hydrazine and its derivatives have numerous commercial applications. Itwas used initially as rocket propellant. During World War II, it was used as afuel for rocket-powered fighter planes. However, the most important applications of hydrazine and its derivatives at present are: as blowing agents; forinsect control; in pharmaceuticals; in water treatment; and in fuel cells.Hydrazine derivatives release nitrogen on decomposition, producing foamingaction in polymers to form pores or cells. A large number of hydrazine derivatives are used in agricultural applications as fungicides, herbicides, and pesticides for weed and pest control. A few hydrazide drugs, such as isoniazid [54-85-3] are used extensively for treating tuberculosis. Other applications ofhydrazine include its use in fuel cells; and in wastewater treatment forremoval of iron; iron removal from hot-water heating systems; reduction ofred iron oxide rust into magnetite; and for removal of oxygen to protectagainst corrosion. It also is used in electrolytic plating of metals on glassesand as a reducing agent. Several hydrazine derivatives are used in azo dyes;as coupling agents in color photography; and in explosives and ammunitionprimers. -
Verwenden
Hydrazine is used as a high-energy rocket fuel, as a reducing agent, and for preparing organic hydrazine derivatives. The propellant grade of commercial hydrazine is more than 97.7% active. It is also used as an oxygen scavenger in boiler water. Hydrazine has also been used as an experimental drug for treating tuberculosis and sickle cell anemia. -
Verwenden
Reducing agent for many transition metals and some nonmetals (arsenic, selenium, tellurium), as well as uranium and plutonium; corrosion inhibitor in boiler feedwater and reactor cooling water; waste water treatment; electrolytic plating of metals on glas -
Verwenden
Hydrazine is a highly reactive base and powerful reducing agent. It acts as an oxygen scavenger and is highly reactive with other chemicals. Hydrazine has a number of uses including, as a chemical precursor to blowing agents (e.g., azodicarbonamide and azobisisobutyronitrile), in the organic synthesis of pharmaceuticals and pesticides (e.g., isoniazid, fluconazole, and 3-amino-1,2,4-triazole), as a missile and rocket propellant (e.g., used in the F-16 fighter), as a gas-forming agent in air bags (e.g., sodium nitrite), as a corrosion inhibitor and reducing agent in large industrial boilers, and as a fuel source in fuel cells. -
Vorbereitung Methode
Hydrazine is a colorless, fuming, oily liquid with an ammonia-like odor. It should be stored in glass containers in a cool, dark place.
Hydrazine is prepared commercially by the Raschig and the urea processes. The Raschig method involves reacting sodium hypochlorite with excess ammonia, flash boiling to recover dilute hydrazine, and fractionating to produce the hydrate. In the urea process, urea is oxidized with hypochlorite to produce the hydrate. Both anhydrous hydrazine and the hydrate are fuming, strongly basic (pKb1=5.52), colorless liquids. Hydrazine may ignite under various circumstances (e.g., on contact with rust) and it decomposes violently in contact with oxidizing materials. It is usually stored under nitrogen to reduce the flammability hazard and to maintain purity. -
Definition
hydrazine: A colourless liquid orwhite crystalline solid,N2H4; r.d. 1.01(liquid); m.p. 1.4°C; b.p. 113.5°C. It isvery soluble in water and soluble inethanol. Hydrazine is prepared bythe Raschig synthesis in which ammoniareacts with sodium(I) chlorate(sodium hypochlorite) to give NH2Cl,which then undergoes further reactionwith ammonia to give N2H4. Industrialproduction must be carefullycontrolled to avoid a side reactionleading to NH4Cl. The compound is aweak base giving rise to two series ofsalts, those based on N2H5+, whichare stable in water (sometimes writtenin the form N2H4.HCl rather thanN2H5+Cl-), and a less stable and extensivelyhydrolysed series based onN2H62+. Hydrazine is a powerful reducingagent and reacts violentlywith many oxidizing agents, henceits use as a rocket propellant. It reactswith aldehydes and ketones togive hydrazones. -
Vorbereitung Methode
Although the earlier processes for the commercial production of hydrazine used urea as a raw material, modern processes employ direct ammonia oxidation. In one such process, reactions occur in two steps:
NH3 + NaOCl → NH2Cl + NaOH (1) NH3 + NH2Cl + NaOH → H2N·NH2 + NaCl + H2O. (2)
High-grade hypochlorite is required for Step 1. Special agents, such as gelatin, ethylenediamine tetracetic acid, glue, high alcohols, and formaldehyde, are required to inhibit undesirable side reactions that would reduce the hydrazine yield through formation of ammonium chloride and N2. In another hydrazine process, chlorine, NH3, and H2SO4, along with methylethyl ketone, are used as the charge. The products of this process include hydrazine hydrate, hydrazine sulfate, ketazine, and dialkyldiazacyclopropane. Hydrazine also is used as a start-up ingredient in the preparation of cooling water for nuclear reactors where it is desired to keep the oxygen content of the water to an absolute minimum and thus decrease corrosion. Oxygen reacts with hydrazine. H2N·NH2 + O2 → N2 + 2H2O. When no oxygen is present in the water, the hydrazine acts as a sink for dissolved oxygen that may enter later, by maintaining metal oxides at their lower oxidation states.
In the laboratory, hydrazine can be prepared by converting one-half of a given amount of NH3 into chloramine, NH2Cl, by sodium hypochlorite solution in the presence of a colloid and heating. The remaining one-half of the NH3 reacts with chloramine to form hydrazine. The product is then cooled to 0 °C and H2SO4 added in amount to react with the hydrazine to form hydrazine sulfate, N2H6SO4, insoluble solid. Hydrazine hemisulfate, (N2H5)2SO4, is soluble in H2O. It can also be made by the reaction of NH3 and hydroxylamine-O-sulfonic acid. -
Definition
A colorless liquid that can be prepared by the oxidation of ammonia with sodium chlorate(I) or by the gas phase reaction of ammonia with chlorine. Hydrazine is a weak base, forming salts (e.g. N2H4.HCl) with strong acids. It is a powerful reducing agent, reducing salts of the noble metals to the metal. Anhydrous hydrazine ignites spontaneously in oxygen and reacts violently with oxidizing agents. The aqueous solution, hydrazine hydrate, has been used as a fuel for jet engines and for rockets. -
Allgemeine Beschreibung
Colorless liquid with an ammonia-like odor. A violent poison. Causes delayed eye irritation. Very corrosive, attacks glass, rubber, and cork. Corrodes molybdenum steels such as Allegheny stainless 316.
It is a strong reducing agent and a flammable liquid and vapour. Hydrazine is a useful building block in organic synthesis of pharmaceuticals and pesticides. There are many kinds of hydrazine compounds, including hydrazine, 1,1-dimethylhydrazine, and 1,2-dimethylhydrazine. Small amounts of hydrazine occur naturally in plants. Most hydrazines are manufactured for use as rocket propellants and fuels, boiler water treatments, chemical reactants, medicines, and in cancer research. Hydrazines are highly reactive and easily catch fire. -
Air & Water Reaktionen
Fumes in air. Water soluble. -
Reaktivität anzeigen
HYDRAZINE are strongly basic and are powerful reducing agents. Note that a 64% solution corresponds to the composition hydrazine hydrate (N2H4.H2O). Spontaneous ignition can occur with hydrogen peroxide and nitric acid. Contact with metallic oxide surfaces may lead to flaming decomposition [Haz. Chem. Data (1966)]. The reaction between 2,4-dinitrochlorobenzene and hydrazine hydrate shattered the reaction flask [Wischmeyer 1967]. Spontaneous ignition occurs when nitrous oxide and hydrazine are mixed [Mellor 8, Supp. 2:214(1967)]. Potassium and sodium dichromate react explosively with hydrazine [Mellor 11:234(1946-1947)]. Hydrazine hydrate reacts with stannous chloride to give stannous dihydrazinechloride, which decomposes explosively when heated [Mellor 7:430(1946-1947)]. Explodes during distillation if traces of air are present. Affected by UV and metal ion catalysis [Merck, 11th ed., 1989]. -
Hazard
Severe explosion hazard when exposed to heat or by reaction with oxidizers. Toxic by ingestion, inhalation, and skin absorption; strong irritant to skin and eyes; a confirmed carcinogen. -
Health Hazard
Hydrazine is extremely destructive to the tissues of the mucous membranes and upper respiratory tract, eyes, and skin. Skin contact with the liquid can result in severe burns; hydrazine is readily absorbed through the skin, leading to systemic effects, which may include damage to the liver, kidney, nervous system, and red blood cells. Hydrazine vapor is irritating to the nose, throat, and respiratory tract, and inhalation of high concentrations may be fatal as a result of spasm, inflammation, chemical pneumonitis, and pulmonary edema. Symptoms of exposure may include a burning sensation, coughing, wheezing, laryngitis, shortness of breath, headache, nausea, and vomiting. Hydrazine vapor is extremely irritating to the eyes and can cause temporary blindness. Eye contact with the liquid can result in severe burns and permanent damage. Hydrazine is not considered to have adequate warning properties. Hydrazine is listed by IARC in Group 2B "possible human carcinogen" and is classified as a "select carcinogen" according to the criteria of the OSHA Laboratory Standard.Chronic exposure to subacute levels of hydrazine can cause lethargy, vomiting, tremors, itching and burning of the eyes and skin, conjunctivitis, and contact dermatitis. Hydrazine has been found to exhibit reproductive and developmental toxicity in animal tests. -
Brandgefahr
Flammable/combustible material. May be ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water. -
Flammability and Explosibility
Hydrazine is a flammable liquid (NFPA rating = 3) over a very broad range of vapor concentrations (4.7 to 100%). Hydrazine may undergo autoxidation and ignite spontaneously when brought in contact with porous substances such as rusty surfaces, earth, wood, or cloth. Fires should be extinguished with water spray, carbon dioxide, or dry chemical extinguishers. -
mögliche Exposition
Tumorigen, Mutagen; Reproductive Effector.Because of its strongreducing capabilities, hydrazine is used as an intermediatein chemical synthesis, and in photography and metallurgy.It is also used as a rocket fuel; in the preparation of anticor-rosives; textile agents; pesticides; and as a scavenging agentfor oxygen in boiler water. Hydrazine is widely used inpharmaceutical synthesis. -
Erste Hilfe
If this chemical gets into the eyes, remove anycontact lenses at once and irri gate immediately for at least15 min, occasionally lifting upper and lower lids. Seek med-ical attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Seek medical attention immediately. Ifthis chemical has been inhaled, remove from exposure,begin rescue breathing (using universal precautions, includ-ing resuscitation mask) if breathing has stopped and CPR ifheart action has stopped. Transfer promptly to a medicalfacility. When this chemical has been swallowed, get medi-cal attention. Give large quantities of water and inducevomiting.Do not make an unconscious person vomit.Medical observation is recommended for 24- -48 h afterbreathing overexposure, as pulmonary edema may bedelayed. As first aid for pulmonary edema, a doctor orauthorized paramedic may consider administering a cortico-steroid spray. .Note to physician: Consider pyridoxine (25 mg/kg), whichhas been shown to be an effective anticonvulsant for hydra-zine poisoning. -
Carcinogenicity
Hydrazine and hydrazine sulfate are reasonably anticipated to be human carcinogens based on sufficient evidence of carcinogenicity from studies in experimental animals. -
Environmental Fate
Hydrazine can be found in the environment in small quantities and is a component of tobacco smoke. However, hydrazine is primarily an industrial chemical that enters the environment by emissions from its use as an aerospace fuel and from industrial facilities that manufacture, process, and/or use this chemical. Treatment and disposal of wastes containing hydrazine also contribute to environmental concentrations. However, hydrazine rapidly degrades in the environment and is rarely encountered outside the industrial setting. -
Lager
work with hydrazine should be conducted in a fume hood to prevent exposure by inhalation, and splash goggles and impermeable gloves should be worn at all times to prevent eye and skin contact. Hydrazine should be used only in areas free of ignition sources. Hydrazine should be stored under nitrogen in containers placed in secondary containers in areas separate from oxidizers and acids. -
Versand/Shipping
(1) Hydrazine, anhydrous or hydrazine aqueoussolutions with >64% hydrazine, by mass, requires a ship-ping labelof“CORROSIVE,POISONOUS/TOXICMATERIALS." It falls in Hazard Class 8 and PackingGroup I. (2) Hydrazine hydrate or hydrazine aqueous solu-tions, with not . < <37% but not > 64% hydrazine, by mass,requires a shipping label of“CORROSIVE, POISONOUS/TOXIC MATERIALS." It falls in Hazard Class 8 andPacking Group II. (3) Hydrazine, aqueous solution, with not> 37% hydrazine, by mass, requires ashipping label of“COR ROSIVE,POISONOUS/TOXIC MATERIALS.” Itfalls in Hazard Class 6.1 and Packing Group II. -
läuterung methode
Hydrazine hydrate is dried by refluxing with an equal weight of KOH pellets for 3hours, then distilled from fresh solid NaOH or BaO in a current of dry N2. Use stainless steel or copper equipment. Hydrazine and its hydrates have VERY IRRITATING and TOXIC vapours and should be used in an efficient fume cupboard. Store in a well-stoppered vessel, preferably under N2. It is a reducing agent. [Schenk in Handbook of Preparative Inorganic Chemistry (Ed. Brauer) Academic Press Vol I pp 469-472 1963.] -
Toxicity evaluation
Hydrazine is strongly corrosive and therefore severely irritates the skin, eyes, and mucous membranes. Systemic toxicity observed after hydrazine exposure is thought to be the result of several possible mechanisms including:
1. Corrosive actions directly with tissue.
2. The reaction of hydrazine with endogenous alpha-keto acids such as vitamin B, (pyridoxine). The formation of hydrazones of pyridoxine is the proposed mechanism by which hydrazine produces the neurological effects observed after exposure.
3. The generation of free radical intermediates, which have been detected during the metabolism of hydrazine in vitro.
The carcinogenicity of hydrazine is believed to be a result of the condensation of hydrazine with endogenous formaldehyde forming a formaldehyde hydrazone, which is further metabolized to a potent DNA methylating agent causing the formation of methylated DNA and transcription errors. -
Inkompatibilitäten
Hydrazine is a highly reactive reducing agent that forms shock-sensitive, explosive mixtures with many compounds. It explodes on contact with barium oxide, calcium oxide, chromate salts, and many other substances. On contact with metal catalysts (platinum black, Raney nickel, etc.), hydrazine decomposes to ammonia, hydrogen, and nitrogen gases, which may ignite or explode. -
Waste disposal
In the event of a spill, remove all ignition sources, soak up the hydrazine with a spill pillow or absorbent material, place in an appropriate container, and dispose of properly. Evacuation and cleanup using respiratory protection may be necessary in the event of a large spill or release in a confined area. Disposal Excess hydrazine and waste material containing this substance should be placed in an appropriate container, clearly labeled, and handled according to your institution's waste disposal guidelines. For more information on disposal procedures, see Chapter 7 of this volume.
HYDRAZINE Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
- Benzophenonhydrazon
- 1-(4-Methoxybutyl)hydrazine
- Ethylcarbazat
- 1-(Tetrahydro-2H-pyran-4-yl)hydrazine
- (4-OXO-3,4-DIHYDROPHTHALAZIN-1-YL)ACETIC ACID
- 1-(4-Morpholinobutyl)hydrazine
- 2-Hydrazinyl-1-morpholinoethanone
- 3-(N,N-Dimethylcarbamoylimido)-1,1-dimethylharnstoff
- 1-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID
- 6-Amino-1H-pyrimidin-4-on
- 4-HYDRAZINO-6-HYDROXYPYRIMIDINE
- (2-MORPHOLIN-4-YL-ETHYL)-HYDRAZINE
- 3-Amino-1H-pyrazol-4-carbonsure
- Vindesin
- 1-(3-(pyrrolidin-1-yl)propyl)hydrazine
- 3-Hydrazinyl-1-(4-methylpiperazin-1-yl)propan-1-one
- (TETRAHYDRO-FURAN-2-YLMETHYL)-HYDRAZINE
- 5-(2-aminoethyl)-4-methylthiazol-2-ol
- Ethyl-3-amino-1H-pyrazol-4-carboxylat
- (2-PYRROLIDIN-1-YL-ETHYL)-HYDRAZINE
- 2-Hydrazino-4-(trifluoromethyl)pyrimidine
- 3-MERCAPTOPICOLINIC ACID
- 5-CYCLOPROPYL-2H-PYRAZOL-3-YLAMINE
- ETHYL 5-AMINO-3-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLATE
- 4-CHLORO-2-(TRIFLUOROMETHYL)PYRIMIDINE-5-CARBONITRILE
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