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1601500

USP

Residual Solvent Class 2 - N,N-Dimethylformamide

United States Pharmacopeia (USP) Reference Standard

Synonyma:

N,N-Dimethylformamide solution

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About This Item

Empirický vzorec (Hillův zápis):
C3H7NO
Číslo CAS:
68-12-2
Molekulová hmotnost:
73.09
MDL number:
MFCD00003284
UNSPSC Code:
41116107
NACRES:
NA.24

grade

pharmaceutical primary standard

manufacturer/tradename

USP

application(s)

pharmaceutical (small molecule)

format

neat

SMILES string

N(C)(C)C=O

InChI

1S/C3H7NO/c1-4(2)3-5/h3H,1-2H3

InChI key

ZMXDDKWLCZADIW-UHFFFAOYSA-N

General description

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.

Application

Residual Solvent Class 2 - N,N-Dimethylformamide USP reference standard, intended for use in specified quality tests and assays as specified in the USP compendia.

Analysis Note

These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.  ​

Other Notes

Sales restrictions may apply.

related product

Č. produktu
Popis
Stanovení ceny

pictograms

Health hazard
GHS08

signalword

Danger

hcodes

H360D

Hazard Classifications

Repr. 1B

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 1

flash_point_f

188.6 °F - closed cup

flash_point_c

87 °C - closed cup

Seznamy omezení vyplývajících z předpisů

Seznamy omezení vyplývajících z předpisů jsou poskytovány zejména pro chemické produkty. Pro jiné než chemické produkty lze poskytovat pouze omezené informace. Žádný záznam znamená, že v seznamech není obsažena žádná ze součástí. Povinností uživatele je zajistit bezpečné a zákonné použití produktu.

EU REACH SVHC Candidate List

CAS No.

EU REACH Annex XVII (Restriction List)

CAS No.

Vyberte jednu z posledních verzí:

Osvědčení o analýze (COA)

Lot/Batch Number

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N,N-Dimethylformamide for analysis EMSURE® ACS,ISO,Reag. Ph Eur

Supelco

1.03053

N,N-Dimethylformamide

N,N-Dimethylformamide anhydrous, 99.8%

Sigma-Aldrich

227056

N,N-Dimethylformamide

N,N-Dimethylformamide for molecular biology, ≥99%

Sigma-Aldrich

D4551

N,N-Dimethylformamide

N,N-Dimethylformamide suitable for HPLC, ≥99.9%

Sigma-Aldrich

270547

N,N-Dimethylformamide

N,N-Dimethylformamide EMPLURA®

Supelco

8.22275

N,N-Dimethylformamide

N,N-Dimethylformamide EMPARTA®

Supelco

1.03034

N,N-Dimethylformamide

K Tanaka et al.
Sangyo igaku. Japanese journal of industrial health, 24(1), 3-12 (1982-01-01)
Industrial use of N, N-dimethylformamide (DMF) is increasing in recent years. The toxic properties of this substance are reviewed from the standpoint of industrial hygiene. Hepatotoxicity has been emphasized by many authors. Care should be taken against the skin absorption
Metabolism of N,N-dimethylformamide: key to the understanding of its toxicity.
A Gescher
Chemical research in toxicology, 6(3), 245-251 (1993-05-01)
Cui Wang et al.
Environmental pollution (Barking, Essex : 1987), 190, 133-138 (2014-04-22)
Occupational and experimental studies have revealed the organs most affected by dimethylformamide (DMF) are liver and gastrointestinal tract. However, few studies have focused on the potential effect of outdoor pollution of DMF. This study examined the health risk of hospitalization
Shengtao Ding et al.
Angewandte Chemie (International ed. in English), 51(37), 9226-9237 (2012-08-30)
Often used as a common solvent for chemical reations and utilized widely in industry as a reagent, N,N-dimethylformamide (DMF) has played an important role in organic synthesis for a long time. Numerous highly useful articles and reviews discussing its utilizations
Xiaowen Xu et al.
Organic letters, 16(13), 3540-3543 (2014-06-17)
A novel straightforward synthesis of both symmetrical and unsymmetrical 2,4-disubstituted-1,3,5-triazines via aerobic copper-catalyzed cyclization of amidines with DMF as a one-carbon synthon has been developed. The presented method allows synthesizing the products that are currently inaccessible or challenging to prepare

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