推荐产品
等级
SAJ special grade
表单
aqueous solution
存货情况
available only in Japan
浓度
0.0282 M
0.0282 N
储存温度
15-25°C
SMILES字符串
[Ag]
InChI
1S/Ag.NO3/c;2-1(3)4/q+1;-1
InChI key
SQGYOTSLMSWVJD-UHFFFAOYSA-N
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警示用语:
Danger
危险声明
危险分类
Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 1B
储存分类代码
6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Ali Hebeish et al.
Carbohydrate polymers, 92(1), 407-413 (2012-12-12)
Innovative CMC-based hydrogels with great potentials for usage in medical area were principally synthesized as per two strategies .The first involved reaction of epichlorohydrin in alkaline medium containing silver nitrate to yield silver nano-particles (AgNPs)-loaded CMC hydrogel. While CMC acted
Liming Wang et al.
ACS nano, 9(6), 6532-6547 (2015-05-23)
To predict potential medical value or toxicity of nanoparticles (NPs), it is necessary to understand the chemical transformation during intracellular processes of NPs. However, it is a grand challenge to capture a high-resolution image of metallic NPs in a single
Irina Blinova et al.
Environmental science and pollution research international, 20(5), 3456-3463 (2012-11-13)
Although silver nanoparticles (NPs) are increasingly used in various consumer products and produced in industrial scale, information on harmful effects of nanosilver to environmentally relevant organisms is still scarce. This paper studies the adverse effects of silver NPs to two
Benjamin P Colman et al.
PloS one, 8(2), e57189-e57189 (2013-03-08)
A large fraction of engineered nanomaterials in consumer and commercial products will reach natural ecosystems. To date, research on the biological impacts of environmental nanomaterial exposures has largely focused on high-concentration exposures in mechanistic lab studies with single strains of
Tao Xu et al.
Organic letters, 14(21), 5416-5419 (2012-10-24)
A silver-catalyzed intramolecular oxidative aminofluorination of alkynes has been developed by using NFSI as a fluorinating reagent. This reaction represents an efficient method for the synthesis of various 4-fluoroisoquinolines and 4-fluoropyrrolo[α]isoquinolines.
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