1,2-Dihydro-5-nitroacenaphthylen

5-Nitroacenaphthene

HCID 11769CAS 602-87-9

Grundinformationen

Standard-SMILES
O=[N+]([O-])c1ccc2c3c(cccc13)CC2
InChIKey
CUARLQDWYSRQDF-UHFFFAOYSA-N
Summenformel
C12H9NO2
Durchschnittliche Molmasse
199,2 g/mol
Monoisotopische Masse
199,06332853

Überblick

5-Nitroacenaphthene can cause cancer according to an independent committee of scientific and health experts.

Namen und Bezeichner

Bevorzugter Name
5-Nitroacenaphthene
IUPAC
5-nitro-1,2-dihydroacenaphthylene
Lokaler Name
1,2-Dihydro-5-nitroacenaphthylen
Englischer Name
5-Nitroacenaphthene
Summenformel
C12H9NO2
Molmasse
199.21

Namen und Synonyme

5-NITROACENAPHTHENE602-87-95-NitroacenaptheneAcenaphthylene, 1,2-dihydro-5-nitro-Acenaphthene, 5-nitro-5-Nan5-Nitronaphthalene ethyleneNCI-C01967DTXSID30209601,2-Dihydro-5-nitroacenaphthyleneF023F6C79XNSC-1312
Weitere Namen anzeigen
5-NitroaceNitroacenaphthene5-nitro-acenaphthenTrofinetide Impurity 14
NSC-22421DTXCID10960RefChem:103262210-025-05-Nitro-1,2-dihydroacenaphthylene1,2-Dihydro-5-nitro-acenaphthyleneMFCD000142775-Nitronaphthalene

Datenbank-Bezeichner

CAS
602-87-9
PubChem CID
11769
DTXSID
DTXSID3020960
ChEMBL
CHEMBL423081
ChEBI
CHEBI:82350
UNII
F023F6C79X
EC Number
210-025-0
Nikkaji
J40.490J

Eigenschaften

Berechnete Struktureigenschaften

XLogP
3,9
Polarare Oberfläche (TPSA)
45,8 Ų
H-Brücken-Donoren
0
H-Brücken-Akzeptoren
2
Frei drehbare Bindungen
0
Schwere Atome
15

Experimentelle und physikochemische Eigenschaften

Chemical ClassesCarcinogens
PolymersOther Classes -> Polycyclic Aromatic Hydrocarbons
SpringerMaterials Properties13C nuclear magnetic resonance spectrum
LogP · 2 Einträge

log Kow = 3.85

3.85

Color/FormSolid
Solubility · 4 Einträge

less than 1 mg/mL at 68 °F (NTP, 1992)

Soluble in ethanol, ethyl ether, ligroin

Soluble in hot water

In water, 0.91 mg/L at 25 °C

Physikochemische Eigenschaften

Schmelzpunkt
100 · 100-101 °C(lit.)
Siedepunkt
279 °C · 279°C
Dichte
1.1919 · 1.1919 (rough estimate)
Brechungsindex
1.588 · 1.5880 (estimate)
Flammpunkt
279 °C · 279°C
storage temp.
-20 °C · -20°C Freezer

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 6 Einträge

Danger

H350: May cause cancer [Danger Carcinogenicity]

P203, P280, P318, P405, and P501 (click each P-code to see the statement)

Danger

H350 (100%): May cause cancer [Danger Carcinogenicity]

P203, P280, P318, P405, and P501 (click each P-code to see the statement)

Gefahrenhinweise

Regulatory Information · 2 Einträge

Hazard Traits - Carcinogenicity

The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)

DOT LabelPoison
Fire HazardsFlash point data for this chemical are not available. It is probably combustible. (NTP, 1992)
Health HazardsACUTE/CHRONIC HAZARDS: There is clear evidence that this compound is an animal carcinogen. When heated to decomposition it emits toxic fumes of NOx. (NTP, 1992)
Hazards SummaryAn irritant; [MSDSonline] See 1-Nitropyrene.
Reactive GroupHydrocarbons, Aromatic

Sicherheit und Schutzausrüstung

Fire FightingFires involving this material can be controlled with a dry chemical, carbon dioxide or Halon extinguisher. (NTP, 1992)
First Aid · 1 Eintrag

EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.

Storage Conditions · 1 Eintrag

PRECAUTIONS FOR "CARCINOGENS": Storage site should be as close as practical to lab in which carcinogens are to be used, so that only small quantities required for ... expt need to be carried. Carcinogens should be kept in only one section of cupboard, an explosion-proof refrigerator or freezer (depending on chemicophysical properties ...) that bears appropriate label. An inventory ... should be kept, showing quantity of carcinogen & date it was acquired ... Facilities for dispensing ... should be contiguous to storage area. /Chemical Carcinogens/

Cleanup Methods · 1 Eintrag

PRECAUTIONS FOR "CARCINOGENS": A high-efficiency particulate arrestor (HEPA) or charcoal filters can be used to minimize amt of carcinogen in exhausted air ventilated safety cabinets, lab hoods, glove boxes or animal rooms ... Filter housing that is designed so that used filters can be transferred into plastic bag without contaminating maintenance staff is avail commercially. Filters should be placed in plastic bags immediately after removal ... The plastic bag should be sealed immediately ... The sealed bag should be labelled properly ... Waste liquids ... should be placed or collected in proper containers for disposal. The lid should be secured & the bottles properly labelled. Once filled, bottles should be placed in plastic bag, so that outer surface ... is not contaminated ... The plastic bag should also be sealed & labelled. ... Broken glassware ... should be decontaminated by solvent extraction, by chemical destruction, or in specially designed incinerators. /Chemical Carcinogens/

Nonfire Spill Response · 1 Eintrag

SMALL SPILLS AND LEAKAGE: If a spill of this chemical occurs, FIRST REMOVE ALL SOURCES OF IGNITION, then you should dampen the solid spill material with acetone and transfer the dampened material to a suitable container. Use absorbent paper dampened with acetone to pick up any remaining material. Seal your contaminated clothing and the absorbent paper in a vapor-tight plastic bag for eventual disposal. Solvent wash all contaminated surfaces with acetone followed by washing with a soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned.

Disposal Methods · 5 Einträge

SRP: Criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.

Carefully incinerate in an incinerator equipped with afterburner and scrubbers. Recommendable method: Incineration... (Peer-review conclusions of an IRPTC expert consultation (May 1985))

PRECAUTIONS FOR "CARCINOGENS": There is no universal method of disposal that has been proved satisfactory for all carcinogenic compounds & specific methods of chem destruction ... published have not been tested on all kinds of carcinogen-containing waste. ... summary of avail methods & recommendations ... /given/ must be treated as guide only. /Chemical Carcinogens/

PRECAUTIONS FOR "CARCINOGENS": ... Incineration may be only feasible method for disposal of contaminated laboratory waste from biological expt. However, not all incinerators are suitable for this purpose. The most efficient type ... is probably the gas-fired type, in which a first-stage combustion with a less than stoichiometric air:fuel ratio is followed by a second stage with excess air. Some ... are designed to accept ... aqueous & organic-solvent solutions, otherwise it is necessary ... to absorb soln onto suitable combustible material, such as sawdust. Alternatively, chem destruction may be used, esp when small quantities ... are to be destroyed in laboratory. /Chemical Carcinogens/

For more Disposal Methods (Complete) data for 5-Nitroacenaphthene (7 total), please visit the HSDB record page.

Toxikologische Informationen

Environmental Fate · 3 Einträge

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 8,000(SRC), determined from a log Kow of 3.9(2) and a regression-derived equation(3), indicates that 5-nitroacenaphthene is expected to be immobile in soil(SRC). Volatilization of 5-nitroacenaphthene from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 1.1X10-6 atm-cu m/mole(SRC), using a fragment constant estimation method(4). 5-Nitroacenaphthene is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 3.9X10-5 mm Hg at 25 °C(SRC), determined from a fragment constant method(5). Biodegradation data were not available(SRC, 2009).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 8,000(SRC), determined from a log Kow of 3.9(2) and a regression-derived equation(3), indicates that 5-nitroacenaphthene is expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is not be expected to be an important environmental fate process(4) based upon an estimated Henry's Law constant of 1.1X10-6 atm-cu m/mole(SRC), developed using a fragment constant estimation method(5). Using this Henry's Law constant and an estimation method(4), volatilization half-lives for a model river and model lake are 110 days and 780 days, respectively(SRC). Moreover volatilization from water surfaces is expected to be attenuated by adsorption to suspended solids and sediment in the water column. The estimated volatilization half-life from a model pond is 62 years if adsorption to soil and sediment is considered(6). According to a classification scheme(7), an estimated BCF of 160(SRC), from its log Kow(2) and a regression-derived equation(8), suggests the potential for bioconcentration in aquatic organisms is high, provided the compound is not metabolized by the organism(SRC). Biodegradation data were not available(SRC, 2009).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), 5-nitroacenaphthene, which has an estimated vapor pressure of 3.9X10-5 mm Hg at 25 °C(SRC), determined from a fragment constant method(2), will exist in both the vapor phase and particulate phase in the ambient atmosphere. Vapor-phase 5-nitroacenaphthene is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 1.9 days(SRC), calculated from its rate constant of 8.3X10-12 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). Particulate-phase 5-nitroacenaphthene will be removed from the atmosphere by wet or dry deposition(SRC). 5-Nitroacenaphthene contains chromophores that absorb at wavelengths >290 nm(4) and therefore may be susceptible to direct photolysis by sunlight(SRC).

Adverse EffectsIARC Carcinogen - Class 3: Chemicals are not classifiable by the International Agency for Research on Cancer.
Ongoing Test Status · 1 Eintrag

The following link will take the user to the National Toxicology Program (NTP) Test Agent Search Results page, which tabulates all of the "Standard Toxicology & Carcinogenesis Studies", "Developmental Studies", and "Genetic Toxicity Studies" performed with this chemical. Clicking on the "Testing Status" link will take the user to the status (i.e., in review, in progress, in preparation, on test, completed, etc.) and results of all the studies that the NTP has done on this chemical.[Available from: http://ntp-apps.niehs.nih.gov/ntp_tox/index.cfm?fuseaction=ntpsearch.searchresults&searchterm=602-87-9]

Medical Surveillance · 1 Eintrag

PRECAUTIONS FOR "CARCINOGENS": Whenever medical surveillance is indicated, in particular when exposure to a carcinogen has occurred, ad hoc decisions should be taken concerning ... /cytogenetic and/or other/ tests that might become useful or mandatory. /Chemical Carcinogens/

Soil Adsorption/Mobility · 1 Eintrag

The Koc of 5-nitroacenaphthene is estimated as 8,000(SRC), using a log Kow of 3.9(1), and a regression-derived equation(2). According to a classification scheme(4), this estimated Koc value suggests that 5-nitroacenaphthene is expected to be immobile in soil.

Atmospheric Concentrations · 1 Eintrag

URBAN/SUBURBAN: 5-Nitroacenaphthene was detected in an unknown number of airborne samples in the atmosphere of Baltimore, Maryland in January 2001 at concentrations ranging from 0.35-0.71 pg/cu m and in July 2001 at concentrations ranging from 14-40 pg/cu m(1). 5-Nitroacenaphthene was also detected in an unknown number of airborne samples in the atmosphere of Fort Meade, Maryland in January 2001 at concentrations ranging from 0.16-0.30 pg/cu m and in July 2001 at concentrations ranging from 3.5-13 pg/cu m(1). 5-Nitroacenaphthene was detected in 4 out of 6 airborne samples in air and diesel particulates collected from Baltimore, Maryland at concentrations ranging from 1.7-37.0 ng/g(2).

Sicherheitsdaten

wgk
3
tsca
TSCA listed
ridadr
2811
hs_code
29049090
RTECS-Nr.
AB1060000
risk_code
45

Chemie und Industrie

Pharmakologische Informationen

Metabolism/Metabolites · 1 Eintrag

The metabolism of ... 5-nitroacenaphthene, by the 9000 x g supernatant from the livers of Aroclor-pretreated rats was studied. The major primary metabolites were 1-hydroxy-5-nitroacenaphthene and 2-hydroxy-5-nitroacenaphthene. These metabolites were oxidized to 1-oxo-5-nitroacenaphthene and 2-oxo-5-nitroacenaphthene, hydroxylated to cis-1,2-dihydroxy-5-nitroacenaphthene and trans-1,2-dihydroxy-5-nitroacenaphthene, and reduced to 1-hydroxy-5-aminoacenaphthene and 2-hydroxy-5-aminoacenaphthene. Reduction of 1- and 2-oxo-5-nitroacenaphthene to 1-oxo- and 2-oxo-5-aminoacenaphthene was also observed. When incubations were carried out in a N2-enriched atmosphere (10% O2 in N2), the major metabolites were 1-hydroxy- and 2-hydroxy-5-nitroacenaphthene and 2-oxo-5-aminoacenaphthene. Selected metabolites were tested for mutagenicity toward Salmonella typhimurium TA 98. The most mutagenic of the metabolites tested, in the presence or absence of rat liver 9000 x g supernatant, were 1-hydroxy-5-nitroacenaphthene and 1-oxo-5-nitroacenaphthene. These results indicate that the 9000 x g supernatant from the livers of Aroclor-pretreated rats is capable of catalyzing both the oxidation and reduction of 5-nitroacenaphthene and that the reduced derivatives of 1-hydroxy- or 2-hydroxy- or 1-oxo- or 2-oxo-5-nitroacenaphthene are proximate mutagens.

Verwendung und Herstellung

Uses · 3 Einträge

Used to make naphthalimide dyes (fluorescent whitening agents) and paper dyes; Not used commercially in the US; [HSDB]

Has not been used commercially in US.

In Japan, it is used as a chemical intermediate, without isolation, to produce naphthalimide dyes, which are used as fluorescent whitening agents. Small amount of 5-nitroacenaphthene is also used to produce paper dye.

U.S. Production · 2 Einträge

(1977) Not produced commercially in US

(1979) Not produced commercially in US

Methods of Manufacturing · 2 Einträge

Nitration of acenaphthene in acetic anhydride using copper or zinc nitrate at 30 °C

It is believed to be produced commercially in Japan by nitration of acenaphthene with nitric acid in sulfuric acid soln.

General Manufacturing InformationAcenaphthylene, 1,2-dihydro-5-nitro-: ACTIVE

Anwendungen

Verwenden5-Nitroacenaphthene is a derivative of acenaphthene, a polycyclic hydrocarbon that has potential to act as polyploidizing agents in plants.

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