HCH (ISO)

Bezeichnung:HCH (ISO)

CAS-Nr608-73-1

Englisch Name:BHC

CBNumberCB7190232

SummenformelC6H6Cl6

Molgewicht290.83

MOL-Datei608-73-1.mol

Synonyma

BHC oder HCH

HCH (ISO)

1,2,3,4,5,6-Hexachlorcyclohexan (Isomerengemisch)

HCH (ISO) physikalisch-chemischer Eigenschaften

Schmelzpunkt	112.75°C
Siedepunkt	373.64°C (rough estimate)
Dichte	1.8700
Brechungsindex	1.5691 (estimate)
Löslichkeit	DMSO (Slightly), Methanol (Slightly)
Aggregatzustand	Powder or Flakes
Farbe	White,crystalline powder
Wasserlöslichkeit	31.4mg/L(25 ºC)
Expositionsgrenzwerte	PC-TWA: 0.3 mg/m3; PC-STEL: 0.5 mg/m3
EPA chemische Informationen	1,2,3,4,5,6-Hexachlorocyclohexane (608-73-1)

Sicherheit

Kennzeichnung gefährlicher	T,N
R-Sätze:	21-25-40-50/53-64-48/22-20/21
S-Sätze:	22-36/37-45-60-61
RIDADR	2761
WGK Germany	3
RTECS-Nr.	GV4375000
HazardClass	6.1(b)
PackingGroup	III
Giftige Stoffe Daten	608-73-1(Hazardous Substances Data)
Toxizität	otr-rat-orl 875 mg/kg/7W-I CRNGDP 5,479,84

Gefahreninformationscode (GHS)

BHC Chemische Eigenschaften,Einsatz,Produktion Methoden

ERSCHEINUNGSBILD
WEISSE BIS BRäUNLICHE FLOCKEN ODER PULVER MIT CHARAKTERISTISCHEM GERUCH.
CHEMISCHE GEFAHREN
Zersetzung beim Erhitzen unter Bildung hochgiftiger Rauche mit Phosgen (ICSC 0007), Chlor (ICSC 0126) und Chlorwasserstoff (ICSC 0163), sowie bei Kontakt mit Alkalien.
ARBEITSPLATZGRENZWERTE
TLV: (als gamma-Isomer) 0,5 mg/m?(als TWA); Hautresorption; Krebskategorie A3 (bestätigte krebserzeugende Wirkung beim Tier mit unbekannter Bedeutung für den Menschen); (ACGIH 2005).
MAK: 0,5 mg/m?(Einatembare Fraktion) Spitzenbegrenzung: überschreitungsfaktor II(8); Hautresorption; (DFG 2006).
AUFNAHMEWEGE
Aufnahme in den Körper durch Inhalation des Aerosols, über die Haut und durch Verschlucken.
INHALATIONSGEFAHREN
Verdampfung bei 20°C vernachlässigbar; eine gesundheitsschädliche Partikelkonzentration in der Luft kann jedoch beim Dispergieren schnell erreicht werden.
WIRKUNGEN BEI KURZZEITEXPOSITION
WIRKUNGEN BEI KURZZEITEXPOSITION:
Möglich sind Auswirkungen auf das Zentralnervensystem. Die Auswirkungen treten u.U. verzögert ein. (s.Anm.)
WIRKUNGEN NACH WIEDERHOLTER ODER LANGZEITEXPOSITION
Wiederholter oder andauernder Hautkontakt kann Dermatitis hervorrufen. Möglich sind Auswirkungen auf das Zentralnervensystem, Knochenmark, Leber, Geschlechtshormone und Geschlechtsorgane. Möglicherweise krebserzeugend für den Menschen. Tierversuche zeigen, dass die Substanz möglicherweise fruchtbarkeitsschädigend oder entwicklungsschädigend wirken kann.
LECKAGE
NICHT in die Kanalisation spülen. Verschüttetes Material in Behältern sammeln; falls erforderlich durch Anfeuchten Staubentwicklung verhindern. Reste sorgfältig sammeln. An sicheren Ort bringen. NICHT in die Umwelt gelangen lassen. Persönliche Schutzausrüstung: Atemschutzgerät, P3-Filter für giftige Partikel.
R-Sätze Betriebsanweisung:
R21:Gesundheitsschädlich bei Berührung mit der Haut.
R25:Giftig beim Verschlucken.
R40:Verdacht auf krebserzeugende Wirkung.
R50/53:Sehr giftig für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen haben.
R64:Kann Säuglinge über die Muttermilch schädigen.
R48/22:Gesundheitsschädlich: Gefahr ernster Gesundheitsschäden bei längerer Exposition durch Verschlucken.
R20/21:Gesundheitsschädlich beim Einatmen und bei Berührung mit der Haut.
S-Sätze Betriebsanweisung:
S22:Staub nicht einatmen.
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).
S60:Dieses Produkt und sein Behälter sind als gefährlicher Abfall zu entsorgen.
S61:Freisetzung in die Umwelt vermeiden. Besondere Anweisungen einholen/Sicherheitsdatenblatt zu Rate ziehen.
Chemische Eigenschaften
BHC is a white-to-brownish crystalline solid with a musty, phosgene-like odor.
History
Benzene hexachloride (BHC) was first prepared in 1825, the insecticidal properties were identified in 1944 with the γ-isomer (gamma-isomer), which is about 1,000 times more toxic than any of the other diastereomers formed in the reaction. The structural differences between these individuals are in the orientations of the chlorine atoms with respect to the ring of carbon atoms.
Verwenden
Insecticide.
Definition
An environmentally persistent constituent of a wide variety of agricultural, medical, and veterinary products.
Allgemeine Beschreibung
White to yellow powder or flakes. Musty odor. The gamma isomer is known as lindane, a systemic insecticide. Toxic by ingestion or inhalation.
Reaktivität anzeigen
Halogenated aliphatic compounds, such as HEXACHLOROCYCLOHEXANE, are moderately or very reactive. Reactivity generally decreases with increased degree of substitution of halogen for hydrogen atoms. Materials in this group may be incompatible with strong oxidizing and reducing agents. Also, they may be incompatible with many amines, nitrides, azo/diazo compounds, alkali metals, and epoxides.
Hazard
Highly toxic; questionable carcinogen.
Mechanism of action
Acts as stimulant to the nervous system with contact and stomach action. GABA-gated chloride channel antagonist.
Sicherheitsprofil
Confirmed carcinogen with experimental carcinogenic, neoplastigenic, and tumorigenic data by ingestion and skin contact. Poison by ingestion, skin contact, and subcutaneous routes. Human systemic effects by inhalation: headache, nausea or vomiting, and fever. Implicated in aplastic anemia. Experimental reproductive effects. Mutation data reported. Lindane is more toxic than DDT or dieldrin. Potentially violent reaction with dlmethylformamide + iron. When heated to decomposition it emits highly toxic fumes of phosgene, HCl, and Cl-. See other benzenehexachloride entries. A toxic organochlorine that is persistent in the environment and accumulates in mammalian tissue. For cattle, the oral LD50 <= 100 mg/kg. The various isomers have dlfferent actions; the y (lindane) and a isomers are central nervous system stimulants, the principal symptom being convulsions. The p and A isomers are central nervous system depressants. The use of thermal vaporizers with lindane has caused acute poisoning by inhalation. mixture has been estimated at about 30 g and the dangerous dose of lindane at about 7 to 15 g. However, as already mentioned, a single dose of 45 mg (or approximately 0.65 mg/kg) of lindane caused convulsions. Lindane shows a marked dfference in toxicity to dfferent species. Its toxic effect on laboratory animals compares favorably with that of DDT, but for several domestic animals, notably calves, hdane is more toxic than DDT or Qeldrin. On a chronic systemic basis the a, p and y isomers are experimental carcinogens. Has been implicated in aplastic anemia. Dermatitis and perhaps other manifestations based on sensitivity represent a sort of chronic, though probably not systemic intoxication, which has been observed in humans. The signs and symptoms of confirmed acute poisoning in humans have paralleled those in experimental animals. These signs and symptoms are: excitation, hyperirritability, loss of equhbrium, clonictonic convulsions, and later depression.There is some evidence that the pulmonary edema and vascular collapse may be of neurogenic origm also. The symptoms in animals systemically poisoned by the yisomer alone are essentially similar to those caused by mixtures, although the onset may be earlier. Workers acutely exposed to high air concentrations of lindane and its decomposition products show headache, nausea, and irritation of eyes, nose, and throat. In rare instances, urticaria has followed exposure to lindane vapor. Unlike the signs and symptoms already mentioned, this allergic manifestation occurs only in susceptible individuals, and usually only after a period of sensitization.
mögliche Exposition
The major commercial usage of BHC is based upon its insecticidal properties. α-BCH is used as an Agricultural chemical, pesticide, pharmaceutical, and veterinary drug. The 7-isomer has the highest acute toxic ity, but the other isomers are not without activity. It is gen erally advantageous to purify the 7-isomer from the less active isomers. The γ-isomer acts on the nervous system of insects, principally at the level of the nerve ganglia. As a result, lindane has been used against insects in a wide range of applications including treatment of animals, buildings, humans for ectoparasites, clothes; water for mosquitoes; living plants; seeds and soils. Some applications have been abandoned due to excessive residues, e.g., stored food stuffs. By voluntary action, the principal domestic producer of technical grade BHC requested cancellation of its BHC registrations on September 1, 1976. As of July 21, 1978, all registrants of pesticide products containing BHC voluntar ily canceled their registrations or switched their former BHC products to lindane formulations.
Carcinogenicity
A bioassay of lindane of the NCI was published in 1977. The compound was administered for 80 weeks to groups of Osborne–Mendel rats and B6C3F1 mice. Time-weighted dietary levels for male rats were 236 or 472 ppm; for female rats, 135 or 270 ppm; and for male and female mice, 80 or 160 ppm. Results were as follows: in rats, no tumors occurred at a statistically significant incidence in the treated groups of either sex but (2) in mice, the incidence of hepatocellular carcinoma in lowdose males was significant when compared with that in the pooled controls (controls 5/49, low dose 19/49, p = 0.001). This finding, by itself, is insufficient to establish the carcinogenicity of lindane. The incidence of hepatocellular carcinoma in high-dose male mice was not significantly different from that in matched or pooled controls. It is concluded that under the conditions of this bioassay lindane was not carcinogenic for Osborne–Mendel rats or B6C3F1 mice.
As with most other chlorinated insecticides, lindane has been shown to exhibit tumor promotional activity, possibly via inhibition of intercellular communication. Lindane exposures do inhibit formation of liver tumors following exposures to aflatoxin B1, suggesting an activity other than tumor promotion for lindane. Enhancement of enzymatic deactivation of aflatoxin via induction of microsomal enzymes may play a role in this phenomenon.
The combination of lindane’s lack of significant mutagenic activity, its tumor promotional properties, and the lack of epidemiologic evidence suggest that lindane poses a minimal to nonexistent risk of cancer to humans under reasonable and prescribed use conditions.
Versand/Shipping
UN2761 Organochlorine pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials.
Inkompatibilitäten
Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explo sions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. Decomposes on contact with powdered iron, aluminum, zinc, and on contact with strong bases producing trichlorobenzene.
Waste disposal
A process has been developed for the destructive pyrolysis of benzene hexachloride @ 400 500℃ with a catalyst mixture which contains 5 10% of either cupric chloride, ferric chloride; zinc chloride; or aluminum chloride on activated carbon.
Pestizidtyp
Insecticide; Acaricide; Veterinary substance

HCH (ISO) Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

608-73-1, BHC Verwandte Suche:

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