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48554

Supelco

N-Nitrosodi-n-propylamine

analytical standard

Sinónimos:

NDPA

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About This Item

Fórmula empírica (notación de Hill):
C6H14N2O
Número de CAS:
621-64-7
Peso molecular:
130.19
EC Number:
210-698-0
MDL number:
MFCD00013891
UNSPSC Code:
12000000
PubChem Substance ID:
24872091

grade

analytical standard

CofA

current certificate can be downloaded

packaging

ampule of 100 mg

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

storage temp.

2-30°C

SMILES string

CCCN(CCC)N=O

InChI

1S/C6H14N2O/c1-3-5-8(7-9)6-4-2/h3-6H2,1-2H3

InChI key

YLKFDHTUAUWZPQ-UHFFFAOYSA-N

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Categorías relacionadas

Application

N-Nitrosodi-n-propylamine may be used as an analytical reference standard for the determination of the analyte in wastewater samples gas chromatography—triple quadrupole mass spectrometry.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 1B

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

Certificados de análisis (COA)

Lot/Batch Number
LRAD6012
LRAD2497
LRAC9445
LRAC6182
LRAC4197

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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N-Nitrosodiethylamine ISOPAC®

Sigma-Aldrich

N0258

N-Nitrosodiethylamine

Supelco

Supelco

48320-U

N-Nitrosodibutylamine solution

A new method for quantifying N-nitrosamines in wastewater samples by gas chromatography?triple quadrupole mass spectrometry.
Yoon S, et al.
Talanta, 97, 256-261 (2012)
N-Nitrosodi-n-propylamine.
Report on carcinogens : carcinogen profiles, 11, III200-III201 (2004-01-01)
Metabolism of carcinogenic amino derivatives in various species and DNA alkylation by their metabolites.
H A Schut et al.
Drug metabolism reviews, 15(4), 753-839 (1984-01-01)
J F Teiber et al.
Carcinogenesis, 21(8), 1559-1566 (2000-07-27)
The ability of human liver cytochrome P450s to metabolize the environmental carcinogen N-nitrosodi-n-propylamine (NDPA) was investigated. The maximum rate of NDPA depropylation in seven human liver microsomal samples was 1.15 nmol/min/mg (range 0.53-2.60). Troleandomycin, a P450 3A4/5 inhibitor, inhibited depropylation
T Suzuki et al.
Mutation research, 444(2), 259-268 (1999-10-16)
We studied five carcinogens for (a) organ-specific mutagenicity and expression time in the transgenic (TG) mouse mutation assay and (b) clastogenicity in the peripheral blood micronucleus assay in the same mice. Groups of mice were injected intraperitoneally (ip) with N-nitroso-di-n-propylamine
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