2-Nitroso-1-naphthol

HCID 8592CAS 132-53-6

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

2-NITROSO-1-NAPHTHOL132-53-61-Naphthalenol, 2-nitroso-2-Nitrosonaphthol1-Naphthol, 2-nitroso-2-nitroso-1-naphthalenolbeta-Nitroso-alpha-naphtholC.I. 76610CC0S5HO41VCI 76610NSC-5034DTXSID4059625
Weitere Namen anzeigen
ci76610CI NO 10010Nitroso-1-napht2-nitroso-1-naphthoC.I.Oxidation Base 152-Nitroiso-1-Naphthol
beta-NitrosonaphtholRefChem:477238DTXCID4034075205-064-52-nitrosonaphthalen-1-ol1,2-naphthoquinone 2-oxime.beta.-Nitrosonaphtholnitrosonaphthol

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

Experimentelle und physikochemische Eigenschaften

Chemical ClassesNitrogen Compounds -> Other Aromatics (Nitrogen)
SpringerMaterials PropertiesDensity
Vapor Pressure0.0000911 [mmHg]
Physical DescriptionGreen or gold colored powder; [MSDSonline]

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

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 4 Einträge

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 · 2 Einträge

Chemical: 1-Naphthalenol, 2-nitroso-

1-Naphthalenol, 2-nitroso-: Does not have an individual approval but may be used under an appropriate group standard

Hazards SummaryEmergency treatment: Methemoglobinemia; [HSDB] An irritant; [MSDSonline]
Hazard Classes and CategoriesSkin Irrit. 2 (97.8%)

Sicherheit und Schutzausrüstung

Cleanup Methods · 1 Eintrag

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

Adverse EffectsMethemoglobinemia - The presence of increased methemoglobin in the blood; the compound is classified as secondary toxic effect
Non-Human Toxicity ValuesLD50 MICE INTRAPERITONEAL 42.30 MG/KG

Sicherheitsdaten

F
8
wgk
3
tsca
TSCA listed
hs_code
2929900090
RTECS-Nr.
QL4550000
risk_code
36/37/38

Chemie und Industrie

Pharmakologische Informationen

Metabolism/Metabolites · 1 Eintrag

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 · 3 Einträge

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 · 2 Einträge

(1979) No Data

(1981) No Data

U.S. Imports · 2 Einträge

(1979) No Data

(1981) No Data

U.S. Production · 2 Einträge

(1979) NO EVIDENCE OF COMMERCIAL PRODN IN U.S.

(1981) NO EVIDENCE OF COMMERCIAL PRODN IN U.S.

Methods of ManufacturingPROBABLY BY REACTION OF 1-NAPHTHOL WITH SODIUM NITRITE
General Manufacturing Information · 4 Einträge

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.

Anbieter50 Anbieter

国药集团化学试剂有限公司86-21-63210123 · [email protected]
梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
阿诺西(上海)生物技术有限公司400-1107768 15058188853 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
湖南韵邦生物科技股份有限公司85561037 15386497078 · [email protected]

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