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Merck
CN

72586

Supelco

亚硝酸根离子标准溶液

0.1 M NO2-, for ion-selective electrodes

别名:

亚硝酸钠 溶液

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About This Item

线性分子式:
NaNO2
CAS号:
分子量:
69.00
MDL编号:
UNSPSC代码:
26111700
PubChem化学物质编号:
NACRES:
NB.61
等级:
for ion-selective electrodes
表单:
solution

等级

for ion-selective electrodes

质量水平

表单

solution

保质期

limited shelf life, expiry date on the label

浓度

0.1 M NO2-

密度

1.00 g/mL at 20 °C

储存温度

2-8°C

SMILES字符串

[Na+].[O-]N=O

InChI

1S/HNO2.Na/c2-1-3;/h(H,2,3);/q;+1/p-1

InChI key

LPXPTNMVRIOKMN-UHFFFAOYSA-M

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一般描述

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制备说明

由 NaNO2 和 H2O 配制而成

储存分类代码

12 - Non Combustible Liquids

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Gina Ambrosio et al.
Scientific reports, 10(1), 4114-4114 (2020-03-07)
Chemical reaction with diazonium molecules has revealed to be a powerful method for the surface chemical modification of graphite, carbon nanotubes and recently also of graphene. Graphene electronic structure modification using diazonium molecules is strongly influenced by graphene growth and
null
Edward H Oldfield et al.
Journal of neurosurgery, 119(3), 634-641 (2013-05-28)
Intravenous sodium nitrite has been shown to prevent and reverse cerebral vasospasm in a primate model of subarachnoid hemorrhage (SAH). The present Phase IIA dose-escalation study of sodium nitrite was conducted to determine the compound's safety in humans with aneurysmal
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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