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1601500

USP

Lösungsmittelrückstände Klasse 2 - N,N-Dimethylformamid

United States Pharmacopeia (USP) Reference Standard

Synonym(e):

N,N-Dimethylformamid -Lösung

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About This Item

Empirische Formel (Hill-System):
C3H7NO
CAS-Nummer:
68-12-2
Molekulargewicht:
73.09
UNSPSC-Code:
41116107
NACRES:
NA.24

Qualität

pharmaceutical primary standard

Hersteller/Markenname

USP

Anwendung(en)

pharmaceutical (small molecule)

Format

neat

InChI

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

InChIKey

ZMXDDKWLCZADIW-UHFFFAOYSA-N

Verwandte Kategorien

Allgemeine Beschreibung

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.

Anwendung

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.

Hinweis zur Analyse

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.  ​

Sonstige Hinweise

Sales restrictions may apply.

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Piktogramme

Health hazard
GHS08

Signalwort

Danger

H-Sätze

H360D

Gefahreneinstufungen

Repr. 1B

Lagerklassenschlüssel

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

WGK

WGK 1

Flammpunkt (°F)

188.6 °F - closed cup

Flammpunkt (°C)

87 °C - closed cup

Zulassungslistungen

Zulassungslistungen werden hauptsächlich für chemische Produkte erstellt. Für nicht-chemische Produkte können hier nur begrenzte Angaben gemacht werden. Kein Eintrag bedeutet, dass keine der Komponenten gelistet ist. Es liegt in der Verantwortung des Benutzers, die sichere und legale Verwendung des Produkts zu gewährleisten.

EU REACH SVHC Candidate List

CAS No.

EU REACH Annex XVII (Restriction List)

CAS No.

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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N,N-Dimethylformamid anhydrous, 99.8%

Sigma-Aldrich

227056

N,N-Dimethylformamid

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

Sigma-Aldrich

D4551

N,N-Dimethylformamid

N,N-Dimethylformamid EMPLURA®

Supelco

8.22275

N,N-Dimethylformamid

N,N-Dimethylformamid EMPARTA®

Supelco

1.03034

N,N-Dimethylformamid

N,N-Dimethylformamid Meets ACS Specifications, Meets Reagent Specifications for testing USP/NF monographs GR ACS

Supelco

DX1730

N,N-Dimethylformamid

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
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)
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
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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