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Key Documents

48554

Supelco

N-Nitrosodi-n-propylamine

analytical standard

Synonym(s):

NDPA

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10 G
¥3,405.04

¥3,405.04

Available to ship on2025年5月06日Details

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10 G
¥3,405.04

About This Item

Empirical Formula (Hill Notation):
C6H14N2O
CAS Number:
621-64-7
Molecular Weight:
130.19
EC Number:
210-698-0
MDL number:
MFCD00013891
UNSPSC Code:
12352200
PubChem Substance ID:
24872091

¥3,405.04

Available to ship on2025年5月06日Details

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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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Show Differences

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This Item
69875199958800396
六羰基钼 ≥99.9% trace metals basis

577766

六羰基钼

六羰基钼 technical

69875

六羰基钼

六羰基钼 98%

199958

六羰基钼

Hexacarbonylmolybdenum for synthesis

800396

Hexacarbonylmolybdenum

assay

≥99.9% trace metals basis

assay

-

assay

98%

assay

-

form

solid

form

solid

form

solid

form

powder

mp

150 °C (dec.) (lit.)

mp

150 °C (dec.) (lit.)

mp

150 °C (dec.) (lit.)

mp

147-152 °C (decomposition)

density

1.96 g/mL at 25 °C (lit.)

density

1.96 g/mL at 25 °C (lit.)

density

1.96 g/mL at 25 °C (lit.)

density

1.96 g/cm3 at 20 °C

vapor density

9.1 (vs air)

vapor density

9.1 (vs air)

vapor density

9.1 (vs air)

vapor density

-

bp

156 °C (lit.)

bp

156 °C (lit.)

bp

156 °C (lit.)

bp

-

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.[1]
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Signal Word

Danger

Hazard Statements

H302,H350,H411

Hazard Classifications

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

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves
  • Specification Sheet

    • Choose from one of the most recent versions:

    Certificates of Analysis (COA)

    Lot/Batch Number
    LC26917V
    LC23094V
    LC17383V
    LC11778V
    LC05930V

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    S M Billedeau et al.
    Journal - Association of Official Analytical Chemists, 67(3), 557-562 (1984-05-01)
    A rapid and sensitive procedure is described for determining 4 N-nitrosodialkylamines (dimethyl, diethyl, dipropyl, and dibutyl) and the N-nitroso analogs of piperidine, pyrrolidine, and morpholine in animal feed. The volatile N-nitrosamines were isolated by using a modified high temperature purge
    D Wotherspoon et al.
    Journal - Association of Official Analytical Chemists, 71(2), 333-336 (1988-03-01)
    A quick method for determining N-nitrosodipropylamine (NDPA) levels in trifluralin emulsifiable concentrate formulations is described. At least 18 samples can be analyzed at one time in a minimum of fumehood space, with up to 90% savings on solvents and materials.
    J G Farrelly et al.
    Carcinogenesis, 5(8), 1015-1019 (1984-08-01)
    Nitrosodiallylamine has been reported to be non-carcinogenic in rats while nitrosodipropylamine and nitrosodiethanolamine are liver carcinogens. That nitrosodipropylamine is metabolized at the alpha-position by liver microsomes from Fischer-344 rats supports the widely held contention that such metabolism is responsible for
    A Martelli et al.
    Cancer research, 48(15), 4144-4152 (1988-08-01)
    Ten carcinogenic N-nitroso compounds were assayed for DNA-damaging activity in primary cultures of human and rat hepatocytes. DNA fragmentation was measured by the alkaline elution technique, and unscheduled DNA synthesis by quantitative autoradiography. Positive dose-related responses in the range of
    K E Appel et al.
    IARC scientific publications, (57)(57), 443-451 (1984-01-01)
    Nitrite was formed on incubation of N-nitrosamines with both microsomal systems and a reconstituted system consisting of cytochrome P-450 and NADPH P-450 reductase from pig liver. Nitrite was not obtained when the nitrosamines were incubated with NADPH P-450 reductase alone
    View All Related Papers

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