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Safety Information

48320-U

Supelco

N-Nitrosodi-n-butylamine solution

certified reference material, 2000 μg/mL in methylene chloride

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Synonym(s):
Dibutyl nitrosamine
CAS Number:
EC Number:
UNSPSC Code:
77101502
NACRES:
NA.24

grade

certified reference material

Quality Level

CofA

current certificate can be downloaded

packaging

ampule of 1 mL

concentration

2000 μg/mL in methylene chloride

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

environmental

format

single component solution

storage temp.

2-30°C

InChI

1S/C8H18N2O/c1-3-5-7-10(9-11)8-6-4-2/h3-8H2,1-2H3

InChI key

YGJHZCLPZAZIHH-UHFFFAOYSA-N

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Application

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

Pictograms

Health hazardExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Central nervous system

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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N-Nitrosamines (15 listings): N-Nitrosodi-n-butylamine.
Report on carcinogens : carcinogen profiles, 12, 303-304 (2011-08-24)
Anis Alam et al.
Molecular and cellular biochemistry, 271(1-2), 177-188 (2005-05-11)
The present investigation is aimed to identify and characterize tumor-associated antigen (TAA) in animals exposed to hepatocarcinogen. Swiss albino mice showed an enhanced expression of an approximately 58 kDa glycoprotein in liver cells upon exposure to a potential hepatocarcinogen N-nitrosodibutylamine
M Mochizuki et al.
Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 117(10-11), 884-894 (1998-01-01)
The metabolic fates of N-butyl-N-(4-hydroxybutyl)nitrosamine (BBN) and N,N-dibutylnitrosamine (DBN) were investigated in the rat and other animal species, to elucidate a possible relationship between metabolism and organotropic carcinogenicity to the urinary bladder of these N-nitrosamines. The principal urinary metabolite of
N-nitrosodi-n-butylamine.
Report on carcinogens : carcinogen profiles, 11, III196-III197 (2004-01-01)
Volatile N-nitrosamines in selected Italian cheeses.
A Dellisanti et al.
Bulletin of environmental contamination and toxicology, 57(1), 16-21 (1996-07-01)

Articles

GC-MS method detects nitrosamines in Valsartan tablets, meeting US FDA guidelines for pharmaceutical quality control.

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