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About This Item
Linear Formula:
NaNO2
CAS Number:
Molecular Weight:
69.00
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
231-555-9
MDL number:
Assay:
99.999% trace metals basis
Form:
solid
InChI
1S/HNO2.Na/c2-1-3;/h(H,2,3);/q;+1/p-1
InChI key
LPXPTNMVRIOKMN-UHFFFAOYSA-M
SMILES string
[Na+].[O-]N=O
assay
99.999% trace metals basis
form
solid
autoignition temp.
914 °F
reaction suitability
core: sodium
impurities
≤15.0 ppm Trace Metal Analysis
mp
271 °C (lit.)
Quality Level
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Application
Sodium nitrite (NaNO2) can be used for a variety of applications, such as:
- corrosion inhibition
- as an effective drug on cyanide poisoning
- inhibiting the growth of micro-organisms
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Aquatic Acute 1 - Eye Irrit. 2 - Ox. Sol. 3
Storage Class
5.1B - Oxidizing hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Thiourea and substituted thioureas as corrosion inhibitors for aluminium in sodium nitrite solution
Subramanyam NC, et al.
Corrosion Science, 34(4), 563-571 (1993)
Jenna L Gordon et al.
Veterinary sciences, 7(2) (2020-04-29)
Neuroblastoma, the most common extracranial solid tumor in children, accounts for 15% of all pediatric cancer deaths. Pharmaceutical applications of S-Nitrosylation, which, under normal conditions is involved with a host of epigenetic and embryological development pathways, have exhibited great potential
Yen-Jung Chen et al.
Antioxidants & redox signaling, 31(2), 109-126 (2018-11-13)
Aims: The coordination of neurons to execute brain functions requires plenty of oxygen. Thus, it is not surprising that
Lucas C Pinheiro et al.
Free radical biology & medicine, 53(4), 701-709 (2012-06-23)
The new pathway nitrate-nitrite-nitric oxide (NO) has emerged as a physiological alternative to the classical enzymatic pathway for NO formation from l-arginine. Nitrate is converted to nitrite by commensal bacteria in the oral cavity and the nitrite formed is then
Paul J Shami et al.
Journal of medicinal chemistry, 49(14), 4356-4366 (2006-07-11)
The literature provides evidence that metabolic nitric oxide (NO) release mediates the cytotoxic activities (against human leukemia and prostate cancer xenografts in mice) of JS-K, a compound of structure R(2)N-N(O)=NO-Ar for which R(2)N is 4-(ethoxycarbonyl)piperazin-1-yl and Ar is 2,4-dinitrophenyl. Here
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