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551384

Formamide solution

suitable for 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
NACRES:
NA.24
PubChem Substance ID:
329758082
UNSPSC Code:
12142201
MDL number:
MFCD00007941
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grade

analytical standard

Quality Level

200

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.

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pictograms

Health hazard
GHS08

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

Class II Designated Chemical Substances

prtr

Group 4: Flammable liquids + Type 3 petroleums + Hazardous rank III + Water insoluble liquid

fsl

Substances Subject to be Indicated Names

ishl_indicated

Substances Subject to be Notified Names

ishl_notified

551384-7IN: + 551384-VAR: + 551384-8IN:4548173355177 + 551384-BULK: + 551384-1EA:

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Certificates of Analysis (COA)

Lot/Batch Number
MBBD7253
MBBD0322
MBBC7859
MBBC4770
MBBC0855

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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
Kathleen Vrolix et al.
Journal of autoimmunity, 52, 101-112 (2014-01-21)
Myasthenia gravis (MG) with antibodies against the acetylcholine receptor (AChR-MG) is considered as a prototypic autoimmune disease. The thymus is important in the pathophysiology of the disease since thymus hyperplasia is a characteristic of early-onset AChR-MG and patients often improve
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