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1-Nitrosopyrrolidin

N-NITROSOPYRROLIDINE Struktur
930-55-2
CAS-Nr.
930-55-2
Bezeichnung:
1-Nitrosopyrrolidin
Englisch Name:
N-NITROSOPYRROLIDINE
Synonyma:
NPYR;NPY1R;NPYY1;n-pyr;NPY1-R;No-Pyr;n-n-pyr;NSC 18797;Nitrosopyrrolidine;N-nitropyrrolidine
CBNumber:
CB8684002
Summenformel:
C4H8N2O
Molgewicht:
100.12
MOL-Datei:
930-55-2.mol

1-Nitrosopyrrolidin Eigenschaften

Siedepunkt:
214 °C(lit.)
Dichte
1.085 g/mL at 25 °C(lit.)
Brechungsindex
n20/D 1.489(lit.)
Flammpunkt:
182 °F
storage temp. 
Sealed in dry,2-8°C
L?slichkeit
Chloroform (Sparingly), Ethyl Acetate, Methanol (Slightly)
Aggregatzustand
Oil
pka
-3.14±0.20(Predicted)
Farbe
Pale Yellow to Yellow
CAS Datenbank
930-55-2(CAS DataBase Reference)
IARC
2B (Vol. 17, Sup 7) 1987
EPA chemische Informationen
N-Nitrosopyrrolidine (930-55-2)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Kennzeichnung gef?hrlicher Xn
R-S?tze: 40
RIDADR  2810
WGK Germany  3
RTECS-Nr. UY1575000
HazardClass  6.1(b)
PackingGroup  III
Giftige Stoffe Daten 930-55-2(Hazardous Substances Data)
Toxizit?t LD50 orally in rats: 900 mg/kg (Druckrey)
Bildanzeige (GHS) GHS hazard pictogramsGHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitssch?dlich bei Verschlucken. Akute Toxizit?t oral Kategorie 4 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P270, P301+P312, P330, P501
H351 Kann vermutlich Krebs verursachen. Karzinogenit?t Kategorie 2 Warnung P201, P202, P281, P308+P313, P405,P501
Sicherheit
P281 Vorgeschriebene pers?nliche Schutzausrüstung verwenden.

1-Nitrosopyrrolidin Chemische Eigenschaften,Einsatz,Produktion Methoden

R-S?tze Betriebsanweisung:

R40:Verdacht auf krebserzeugende Wirkung.

Beschreibung

N-Nitrosopyrrolidine (NPYR) is a nitrosamine compound that is used primarily as a research chemical and is not produced commercially. There is the possibility of generating NPYR after frying in dry-cured bacon. The major amine precursors to NPYR in cooked bacon are free proline in the adipose tissue and to a lesser extent, collagenous connective tissues. When proline peptides were heated with nitrite at pH 3.4, small amounts of NPYR were formed from all tested peptides. There are several potential sources of exposure of man to this group of potent carcinogens. Certain foods were thought to be derived from the interaction of nitrite with secondary amines in the food, either spontaneously or by the agency of bacteria. Recently the possibility that nitrosamines may be formed from secondary amines and nitrite in the gastrointestinal tract has been explored. The acid conditions that prevail in the human stomach favor the nitrosation of dimethylamine. In addition, at neutral pH, many secondary amines can be nitrosated by nitrite or nitrate in the presence of intestinal bacteria, or the cecal contents of the rat, and soluble enzymes which catalyze the N-nitrosation of several secondary amines have been extracted from two microorganisms. The rate of nitrosamine formation depends greatly on the basicity of the amine; the less basic amines such as diphenylamine and pyrrolidine are nitrosated far more readily than the strongly basic dimethylamine and diethylamine.

Chemische Eigenschaften

N-Nitrosopyrrolidine is a yellow liquid.

Verwenden

One of the N-nitroso compounds (NOCs) implicated in human colon carcinogenesis, but the toxicological mechanisms involved have not been elucidated.

Allgemeine Beschreibung

Yellow liquid found in certain food products and tobacco smoke. Probably a carcinogen.

Air & Water Reaktionen

Soluble in water.

Reaktivit?t anzeigen

A cyclic nitrosamine. Nitrated organics, such as N-NITROSOPYRROLIDINE, range from slight to strong oxidizing agents. If mixed with reducing agents, including hydrides, sulfides and nitrides, they may begin a vigorous reaction.

Health Hazard

ACUTE/CHRONIC HAZARDS: Flammable.

Brandgefahr

Combustible.

Sicherheitsprofil

Confirmed carcinogen with experimental carcinogenic, neoplastigenic, and tumorigenic data. Poison by ingestion and subcutaneous routes. Human mutation data reported. When heated to decomposition it emits toxic fumes of NOx. See also N-NITROSO COMPOUNDS.

m?gliche Exposition

N-Nitrosopyrrolidine is a cyclic nitrosamine and a research chemical. Not commercially produced in the U.S.

Carcinogenicity

N-Nitrosopyrrolidine is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in experimental animals.

Environmental Fate

It is a yellow liquid at room temperature. It is totally soluble in water with solubility of 1.00×10+6 mg l-1 and also is soluble in organic liquids and lipids. Log Pow is -0.19 that expected to move readily from water to soil, sediment, or biota. According to Henry’s law constant 4.89×10-8 atmm3 mol-1 and vapor pressure 0.06 mmHg in 20 ℃, volatilization from water and solid surface is expected to be rapid and an important fate process.

Versand/Shipping

UN2810 Toxic liquids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required. UN3082 Environmentally hazardous substances, liquid, n.o.s., Hazard Class: 9; Labels: 9-Miscellaneous hazardous material, Technical Name Required liquid, n.o.s., Hazard Class: 9; Labels: 9-Miscellaneous hazardous material, Technical Name Required

Inkompatibilit?ten

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides.

Waste disposal

Under 40 CFR 261.5 small quantity generators of this waste may qualify for partial exclusion from hazardous waste regulations. Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal.

1-Nitrosopyrrolidin Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


1-Nitrosopyrrolidin Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 123)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Career Henan Chemica Co
+86-0371-86658258 +8613203830695
laboratory@coreychem.com China 30241 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418671 +8618949823763
sales@tnjchem.com China 34553 58
Chemsigma International Co., Ltd.
+86-18136843612 +86-19951791336
info@chemsigma.com China 1350 58
sgtlifesciences pvt ltd
+8617013299288
dj@sgtlifesciences.com China 12373 58
Alfa Chemistry

Info@alfa-chemistry.com United States 24072 58
LEAP CHEM CO., LTD.
+86-852-30606658
market18@leapchem.com China 24727 58
Shanghai Acmec Biochemical Technology Co., Ltd.
+undefined18621343501
product@acmec-e.com China 33338 58
Aladdin Scientific
+1-+1(833)-552-7181
sales@aladdinsci.com United States 57505 58
SHANGHAI KEAN TECHNOLOGY CO., LTD.
+8613817748580
cooperation@kean-chem.com China 40066 58
Mainchem Co., Ltd. +86-0592-6210733
sale@mainchem.com China 32343 55

930-55-2(1-Nitrosopyrrolidin)Verwandte Suche:


  • 1-nitroso-pyrrolidin
  • 1-Pyrrolidinamine, N-nitroso-
  • Nitrosopyrrolidine
  • N-NITROSOPYRROLIDINE ISOPAC
  • Pyrrolidine, 1-nitroso-
  • N-Nitrosopyrolidine
  • 1-Nitrosopyrrolidine,N-Nitrosopyrrolidine, NPYR
  • NSC 18797
  • Neuropeptide Y receptor type 1
  • NPY1R
  • NPY1-R
  • NPYY1
  • n-nitroso-1-pyrrolidinamin
  • N-Nitrosopyrrolidin
  • n-nitrosopyrrolidin[german]
  • n-n-pyr
  • No-Pyr
  • NPYR
  • n-pyr
  • rcrawastenumberu180
  • tetrahydro-n-nitroso-pyrrol
  • N-NITROSOPYRROLIDINE
  • 1-NITROSOPYRROLIDINE
  • 1-Nitrosopyrrolidine(NPYR)
  • N-Nitrosopyrrolidine@5.0 mg/mL in MeOH
  • N-nitrosopyrrolidineSolution,100mg/L,1ml
  • N-Nitrosopyrrolidine@100 μg/mL in Dichloromethane
  • N-nitropyrrolidine
  • N-nitroso-pyrrolidine NPYR3,7
  • N-Nitrosopyrrolidine in dichloromethane
  • 930-55-2
  • Carcinogens
  • Cancer Research
  • BioChemical
  • Mutagenesis Research Chemicals
  • Nitrosamine
  • Nitric Oxide Reagents
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