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Key Documents

N7632

Sigma-Aldrich

N-Nitrosodiethanolamine

Synonym(s):

2,2′-(Nitrosoimino)bisethanol, N,N-Diethanolnitrosamine, Bis(2-hydroxyethyl)nitrosamine, NDELA

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About This Item

Empirical Formula (Hill Notation):
C4H10N2O3
CAS Number:
Molecular Weight:
134.13
Beilstein:
1762620
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.25

form

liquid

Quality Level

impurities

≤10% Isopropanol

storage temp.

2-8°C

SMILES string

OCCN(N=O)CCO

InChI

1S/C4H10N2O3/c7-3-1-6(5-9)2-4-8/h7-8H,1-4H2

InChI key

YFCDLVPYFMHRQZ-UHFFFAOYSA-N

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Application


  • Changes in levels of N-nitrosamine formed from amine-containing compounds during chloramination via photocatalytic pretreatment with immobilized TiO(2): Effect of source water and pH.: In this study, NDELA is used as a standard to examine how the formation of nitrosamines, such as N-Nitrosodiethanolamine, is affected by different water sources and pH levels during water treatment processes (Seid et al., 2022).

  • Monitoring and risk assessment of hazardous chemicals in toy-slime and putty in the Netherlands.: This research focuses on the presence of N-Nitrosodiethanolamine in children′s toys, providing important data for consumer safety and regulatory standards (Braver et al., 2021).

  • On-line solid phase extraction-ultra-high performance liquid chromatography coupled to tandem mass spectrometry for the determination of N-nitrosodiethanolamine in baby shampoo.: Highlights the usage of N-Nitrosodiethanolamine as an analytical standard in application of advanced chromatographic techniques for detecting harmful substances in consumer products, ensuring product safety and regulatory compliance (Tada et al., 2021).

Pictograms

FlameHealth hazard

Signal Word

Danger

Hazard Statements

Hazard Classifications

Carc. 1B - Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

52.9 °F

Flash Point(C)

11.6 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Customers Also Viewed

Richard N Loeppky et al.
Chemical research in toxicology, 15(4), 470-482 (2002-04-16)
The mechanism by which environmentally prevalent N-nitrosodiethanolamine (NDELA) and related 2-hydroxyethyl- or other beta-oxidized nitrosamines initiate the carcinogenic process has remained obscure. (32)P-Postlabeling assays for the pH sensitive glyoxal-deoxyguanosine (gdG) and the O(6)-2-hydroxyethyldeoxyguanosine (OHEdG) DNA adducts have been developed as
R C Schothorst et al.
Analytical and bioanalytical chemistry, 381(3), 681-685 (2005-01-26)
We have developed and validated in-house a liquid chromatography and mass spectrometry (LC-MS-MS) method for determination of N-nitrosodiethanolamine (NDELA) in cosmetics. The sample is diluted with water and then a C18 clean-up is performed. The average recovery of NDELA is
M Futakuchi et al.
Cancer letters, 106(2), 263-269 (1996-09-10)
Potential synergism between four N-nitroso compounds (nitrosomorpholine, nitrosodimethylamine, nitrosodiethanolamine, nitroso-oxazolidine) in rat liver carcinogenesis was examined in the medium-term bioassay. Male F344 rats were initially given diethylnitrosamine (DEN, 200 mg/kg, ip) and beginning 2 weeks later received test chemicals for
Michelle K Dennehy et al.
Chemical research in toxicology, 18(3), 556-565 (2005-03-22)
N-Nitrosodiethanolamine (NDELA) is a bident carcinogen that undergoes both P-450 mediated alpha-hydroxylation and beta-oxidation, leading ultimately to the formation of two prominent DNA adducts, glyoxaldeoxyguanosine (gdG) and O6-2-hydroxyethyldeoxyguanosine (OHEdG), in rat liver. HPLC coupled with electrospray ionization (ESI) and tandem
Alireza Ghassempour et al.
Journal of chromatography. A, 1185(1), 43-48 (2008-02-20)
A high-performance liquid chromatographic (HPLC) method was developed for the determination of N-nitrosodiethanolamine (NDELA), which is a non-volatile N-nitrosoamine. In this method, sodium 1-octanesulfonate has been used as an ion complexation agent for NDELA. The resulting complex was analyzed by

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