Grundinformationen
- Standard-SMILES
O=Nc1ccc2ccccc2c1O- InChIKey
SYUYTOYKQOAVDW-UHFFFAOYSA-N- Summenformel
- C10H7NO2
- Durchschnittliche Molmasse
- 173,17 g/mol
- Monoisotopische Masse
- 173,04767846
Überblick
a carcinogen; structure in first source
Namen und Bezeichner
- Bevorzugter Name
- 2-Nitroso-1-naphthol
- IUPAC
- 2-nitrosonaphthalen-1-ol
- Lokaler Name
- 2-Nitroso-1-naphthol
- Englischer Name
- 2-Nitroso-1-naphthol
- Summenformel
- C10H7NO2
- Molmasse
- 173.17
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
132-53-6、6373-60-0- PubChem CID
- 8592
- DTXSID
DTXSID4059625- UNII
- CC0S5HO41V
- EC Number
- 205-064-5
- Nikkaji
- J1.405.240B、J1.405.241K、J5.571I、J70.154H
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 2,5
- Polarare Oberfläche (TPSA)
- 49,7 Ų
- H-Brücken-Donoren
- 1
- H-Brücken-Akzeptoren
- 3
- Frei drehbare Bindungen
- 0
- Schwere Atome
- 13
- Formalladung
- 0
- Komplexität
- 195
Experimentelle und physikochemische Eigenschaften
Physikochemische Eigenschaften
- Schmelzpunkt
- 150 · 150-155 °C (dec.)(lit.)
- Siedepunkt
- 303.81 °C · 303.81°C (rough estimate)
- Dichte
- 1.2427 · 1.2427 (rough estimate)
- Brechungsindex
- 1.52 · 1.5200 (estimate)
- pka
- 7.47 · 7.47±0.10(Predicted)
- Aggregatzustand
- Solid
- Farbe
- 2 O · Yellow needles from H2O or C6H6
- Geruch (Odor)
- Odorless
- Wasserlöslichkeit
- SLIGHTLY SOLUBLE
- BRN
- 1867919 · 1867919
- InChI
- 1S/C10H7NO2/c12-10-8-4-2-1-3-7(8)5-6-9(10)11-13/h1-6,12H
- InChIKey
- SYUYTOYKQOAVDW-UHFFFAOYSA-N
- SMILES
- Oc1c(ccc2ccccc12)N=O
- CAS Datenbank
- 132 · 132-53-6(CAS DataBase Reference)
- NIST chemische Informationen
- 1 · 1-Naphthalenol, 2-nitroso-(132-53-6)
- EPA chemische Informationen
- 1 · 1-Naphthalenol, 2-nitroso- (132-53-6)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Warning
H315 (97.8%): Causes skin irritation [Warning Skin corrosion/irritation]
P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 46 reports by companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Gefahrenhinweise
Regulatory Information
Chemical: 1-Naphthalenol, 2-nitroso-
1-Naphthalenol, 2-nitroso-: Does not have an individual approval but may be used under an appropriate group standard
Sicherheit und Schutzausrüstung
Cleanup Methods
A NEW ENZYMIC METHOD WAS DEVELOPED FOR THE REMOVAL OF PHENOLS & ANILINES FROM INDUSTRIAL WASTEWATERS. THIS INVOLVES THE TREATMENT OF AQ SOLN CONTAINING THE POLLUTANTS WITH HORSERADISH PEROXIDASE & H2O2. SUCH TREATMENT RESULTS IN PPTN OF PHENOLS & AROMATIC AMINES FROM WATER AS A RESULT OF THEIR ENZYMIC CROSSLINKING.
Toxikologische Informationen
Sicherheitsdaten
- F
- 8
- wgk
- 3
- tsca
- TSCA listed
- hs_code
- 2929900090
- RTECS-Nr.
- QL4550000
- risk_code
- 36/37/38
- Toxizität
- LD orl-rat: >500 mg/kg NCNSA6 5,35,53
- hazard_code
- Xi
- safety_code
- 26
- Speicherklasse
- 11 - Combustible Solids
- Giftige Stoffe Daten
- 132-53-6(Hazardous Substances Data)
Chemie und Industrie
Pharmakologische Informationen
Metabolism/Metabolites
PARTIALLY PURIFIED, UNTREATED RAT LIVER CYTOSOL CONTAINS AT LEAST 2 ENZYMES WHICH RAPIDLY REDUCE THE C-NITROSO CARCINOGEN, 2-NITROSO-1-NAPHTHOL IN THE PRESENCE OF NADPH OR NADH AT PH 6-7. 2-NITROSO-1-NAPHTHOL WAS NOT REDUCED BY RAT KIDNEY OR BRAIN CYTOSOL, PLASMA, OR HEMOGLOBIN.
Verwendung und Herstellung
Uses
Used as a dye oxidation base for fur, cotton, jute, and viscose; [HSDB]
Fur Dressing and Dyeing [Category: Industry]
OXIDATION BASE FOR DYE-EG, FOR FUR, COTTON, JUTE, VISCOSE
U.S. Exports
(1979) No Data
(1981) No Data
U.S. Imports
(1979) No Data
(1981) No Data
U.S. Production
(1979) NO EVIDENCE OF COMMERCIAL PRODN IN U.S.
(1981) NO EVIDENCE OF COMMERCIAL PRODN IN U.S.
General Manufacturing Information
1-Naphthalenol, 2-nitroso-: ACTIVE
A 0.5% 2-NITROSO-1-NAPHTHOL SOLN IN DIMETHYL CARBONATE WAS STUDIED FOR ITS POTENTIAL AS TRACE METAL DETECTION REAGENT. A METAL OBJECT MUST BE HELD FOR APPROX 1.5 MIN FOR SATISFACTORY COLOR & PATTERN FORMATION TO BE OBSERVED BY THIS PROCEDURE. BEST RESULTS WERE OBTAINED ON INDIVIDUALS WITH HIGH LEVELS OF PERSPIRATION.
HYDROGEN SULFIDE IS REMOVED FROM WASTE GAS BY CATALYTIC OXIDATION WITH A NONTOXIC ALKALINE SOLN CONTAINING AN AROMATIC NITROSO COMPD, A HYDROXY AMINO COMPD, AN FE SALT, & A CHELATING AGENT; & THE SPENT SOLN IS REGENERATED BY OXIDATION WITH A GAS CONTAINING OXYGEN. THUS, A WASTE GAS CONTAINING 3300 PPM H2S WAS SCRUBBED COUNTERCURRENTLY WITH A SOLN (PH 9) CONTAINING 0.01 MOL EACH OF 2-NITROSO-1-NAPHTHOL (IN 4-SULFONIC ACID), FESO4, EDTA, & CITRIC ACID IN A TOWER CONTAINING RASCHIG RINGS.
A TRACE METAL DETECTION TECHNIQUE FOR USE IN FORENSIC SCIENCE IS DESCRIBED WHICH UTILIZES 2-NITROSO-1-NAPHTHOL. A 0.5% SOLN OF 2-NITROSO-1-NAPHTHOL IN METHYL CARBONATE IS SPRAYED ON SKIN AFTER HOLDING VARIOUS METALLIC OBJECTS, WITH THE IMMEDIATE APPEARANCE OF COLOR THAT MAXIMIZES WITHIN MIN. 2-NITROSO-1-NAPHTHOL WAS AS SENSITIVE TO FE & CU AS THE NORMAL REAGENT 8-HYDROXYQUINOLINE, BUT LESS SENSITIVE BY A FACTOR OF APPROX 100 TO ZN.
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