551384
甲酰胺 溶液
suitable for NMR (reference standard), 90% in DMSO-d6 (99.9 atom % D), NMR tube size 5 mm × 8 in.
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关于此项目
经验公式（希尔记法）:
CH3NO
分子量:
45.04
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
12142201
MDL number:
产品名称
甲酰胺 溶液, suitable for NMR (reference standard), 90% in DMSO-d6 (99.9 atom % D), NMR tube size 5 mm × 8 in.
InChI
1S/CH3NO/c2-1-3/h1H,(H2,2,3)
SMILES string
NC=O
InChI key
ZHNUHDYFZUAESO-UHFFFAOYSA-N
grade
analytical standard
assay
99% (CP)
concentration
90% in DMSO-d6 (99.9 atom % D)
technique(s)
NMR: suitable
NMR tube size
5 mm × 8 in.
suitability
suitable for NMR (reference standard)
format
single component solution
Quality Level
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Features and Benefits
15N 灵敏度
Preparation Note
5 mm O.D. tube contains 0.700 mL.
signalword
Danger
hcodes
Hazard Classifications
Carc. 2 - Repr. 1B - STOT RE 2 Oral
target_organs
Blood
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 2
flash_point_f
190.0 °F - closed cup
flash_point_c
87.8 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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
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
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
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