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Merck

437573

Sigma-Aldrich

N,N-二甲基甲酰胺

ACS reagent, ≥99.8%

别名:

DMF, NSC 5356

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About This Item

线性分子式:
HCON(CH3)2
CAS号:
分子量:
73.09
Beilstein:
605365
EC號碼:
MDL號碼:
分類程式碼代碼:
12352111
PubChem物質ID:

等級

ACS reagent

品質等級

蒸汽密度

2.5 (vs air)

蒸汽壓力

2.7 mmHg ( 20 °C)

化驗

≥99.8%

形狀

liquid

自燃溫度

833 °F

expl. lim.

15.2 %

技術

electrophoresis: suitable

雜質

≤0.0005 meq/g Titr. acid
≤0.003 meq/g Titr. base
≤0.15% water

蒸發殘留物

≤0.005%

顏色

APHA: ≤15

折射率

n20/D 1.430 (lit.)

pH值

6.7

bp

153 °C (lit.)

mp

−61 °C (lit.)

溶解度

water: miscible

密度

0.944 g/mL (lit.)

SMILES 字串

[H]C(=O)N(C)C

InChI

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

InChI 密鑰

ZMXDDKWLCZADIW-UHFFFAOYSA-N

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一般說明

N,N-Dimethylformamide (DMF) is a polar organic solvent with a wide range of industrial applications. It is a precursor for numerous reactions such as formylation, aminocarbonylation, amination, amidation and cyanation. Along with phosphorus oxychloride, it forms Vilsmeier reagent used in the formylation of reactive aromatic and heteroaromatic substrates. Dielectric relaxation experiments on DMF have been conducted between 238.15K and 338.15K. The thermophysical properties of the molecular interactions between DMF and the ionic liquids, ammonium salts and imidazolium salts have been studied. The characteristics of solute-solvent interactions between ammonium nitrate and DMF have been investigated.

應用

N,N-Dimethylformamide (DMF) may be used in the following processes:
  • As a solvent synthesis of gold nanoparticles.
  • As a solvent in capillary electrophoresis.
  • Regioselective synthesis of N,N-dimethylaminopyridzines by reacting with choropyridazines.
  • Synthesis of urea-N,N-dimethylformamide, a 3:1 solvate with urea.
多种疏水性有机化合物的溶剂。

訊號詞

Danger

危險分類

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Eye Irrit. 2 - Flam. Liq. 3 - Repr. 1B

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 2

閃點(°F)

135.5 °F - closed cup

閃點(°C)

57.5 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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分析证书(COA)

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其他客户在看

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Preparation of gold nanoparticles in formamide and N,N-dimethylformamide in the presence of poly (amidoamine) dendrimers with surface methyl ester groups.
Esumi K, et al.
Colloids and Surfaces. A, Physicochemical and Engineering Aspects, 189(1), 155-161 (2001)
Reaction of chloropyridazines with N,N -dimethylformamide.
Lee WS, et al.
Journal of Heterocyclic Chemistry, 37(6), 1591-1591 (2000)
N,N-dimethylformamide as a reaction medium for metal nanoparticle synthesis.
Pastoriza-Santos I and Liz-Marzan LM.
Advances in Functional Materials, 19(5), 679-688 (2009)
Urea-N,N-dimethylformamide (3/1).
Fernandes P, et al.
Acta Crystallographica Section E, Structure Reports Online, 63(12), 4861-4861 (2007)
Capillary electrophoresis in N,N-dimethylformamide.
Porras SP and Kenndler E.
Electrophoresis, 26(17), 3279-3291 (2005)

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