Skip to Content
Merck

551384

Formamide solution

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

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):
CH3NO
Molecular Weight:
45.04
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
12142201
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


grade

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.

suitability

suitable for NMR (reference standard)

format

single component solution

SMILES string

NC=O

InChI

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

InChI key

ZHNUHDYFZUAESO-UHFFFAOYSA-N

Features and Benefits

15N sensitivity

Preparation Note

5 mm O.D. tube contains 0.700 mL.


Still not finding the right product?

Explore all of our products under Formamide solution


pictograms

Health hazard

signalword

Danger

Hazard Classifications

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

target_organs

Blood

Storage Class

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



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library



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
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