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551384

Supelco

Formamide solution

NMR reference standard, 90% in DMSO-d6 (99.9 atom % D), NMR tube size 5 mm × 8 in.

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About This Item

Empirical Formula (Hill Notation):
CH3NO
Molecular Weight:
45.04
MDL number:
UNSPSC Code:
12142201
PubChem Substance ID:
NACRES:
NA.24

grade

NMR reference standard
analytical standard

Quality Level

Assay

99% (CP)

concentration

90% in DMSO-d6 (99.9 atom % D)

technique(s)

NMR: suitable

NMR tube size

5 mm × 8 in.

format

single component solution

SMILES string

NC=O

InChI

1S/CH3NO/c2-1-3/h1H,(H2,2,3)

InChI key

ZHNUHDYFZUAESO-UHFFFAOYSA-N

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Features and Benefits

15N sensitivity

Quantity

5 mm O.D. tube contains 0.700 mL.

Pictograms

Health hazard

Signal Word

Danger

Hazard Statements

Hazard Classifications

Carc. 2 - Repr. 1B - STOT RE 2 Oral

Target Organs

Blood

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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

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