推荐产品
等級
NMR reference standard
analytical standard
品質等級
化驗
99% (CP)
濃度
90% in DMSO-d6 (99.9 atom % D)
技術
NMR: suitable
NRM管尺寸
5 mm × 8 in.
格式
single component solution
SMILES 字串
NC=O
InChI
1S/CH3NO/c2-1-3/h1H,(H2,2,3)
InChI 密鑰
ZHNUHDYFZUAESO-UHFFFAOYSA-N
正在寻找类似产品? 访问 产品对比指南
特點和優勢
15N 灵敏度
數量
5 mm O.D. tube contains 0.700 mL.
訊號詞
Danger
危險分類
Carc. 2 - Repr. 1B - STOT RE 2 Oral
標靶器官
Blood
儲存類別代碼
6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
水污染物質分類（WGK）
WGK 2
閃點（°F）
190.0 °F - closed cup
閃點（°C）
87.8 °C - closed cup
個人防護裝備
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
J Veenemans et al.
Journal of clinical microbiology, 52(7), 2454-2460 (2014-05-03)
Next-generation sequencing (NGS) has the potential to provide typing results and detect resistance genes in a single assay, thus guiding timely treatment decisions and allowing rapid tracking of transmission of resistant clones. We evaluated the performance of a new NGS
Karin Gustafsson et al.
Immunology, 143(1), 33-41 (2014-03-22)
Aberrant regulation of T helper (Th) cell maturation is associated with a number of autoimmune conditions, including allergic disorders and rheumatoid arthritis. The Src homology domain protein B (Shb) adaptor protein was recently implicated as a regulator of Th cell
William R Lovallo et al.
Alcoholism, clinical and experimental research, 38(6), 1575-1581 (2014-05-07)
Central serotonergic (5-HT) function is implicated in pathways to alcohol dependence, including dysphoria manifested by symptoms of anxiety and depression. However, little is known about genetic variation in central 5-HT function and its potential impact on temperament and behavior in
Björn Heindryckx et al.
Mitochondrion, 18, 12-17 (2014-08-28)
To investigate the applicability of preimplantation genetic diagnosis (PGD), we used trophectoderm (TE) biopsy to determine the mutation load in a 35-year-old female with mitochondrial encephalopathy, lactic acidosis and stroke-like syndrome (MELAS). Transfer of a mutation-free blastocyst gave birth to
Elaine Y Liu et al.
Acta neuropathologica, 128(4), 525-541 (2014-05-09)
Hexanucleotide repeat expansions of C9orf72 are the most common genetic cause of amyotrophic lateral sclerosis and frontotemporal degeneration. The mutation is associated with reduced C9orf72 expression and the accumulation of potentially toxic RNA and protein aggregates. CpG methylation is known
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门