N,N-二甲基乙酰胺

Dimethylacetamide

HCID 31374CAS 127-19-5

基本信息

标准SMILES
CC(=O)N(C)C
InChIKey
FXHOOIRPVKKKFG-UHFFFAOYSA-N
分子式
C4H9NO
平均分子量
87.12 g/mol
单同位素质量
87.06841391

名称与标识

首选名称
Dimethylacetamide
IUPAC
N,N-dimethylacetamide
中文名
N,N-二甲基乙酰胺
英文名
N,N-Dimethylacetamide
分子式
C4H9NO
分子量
87.12

名称与别名

N,N-DIMETHYLACETAMIDE127-19-5DimethylacetamideAcetamide, N,N-dimethyl-AcetdimethylamideDMAcDimethyl acetamideN,N-Dimethyl acetamideDimethylamide acetateN,N-DimethylethanamideDimethylacetone amideAcetic acid, dimethylamide
展开更多名称
乙酰二甲胺二甲基醯胺二甲替乙酰胺二甲基乙酰胺HPLC级N气相顶空级NN-乙酰二甲胺N-二甲基乙酰胺N,N-二甲基乙酰甲基丙烯酰化多巴胺DMAN,N-Dimethylacetamide, 99%, pureC4H9NOdimethylacetamidCH3CON(CH3)2Acetic acid dimethylacetamidedimethylacetoneamide
AcetyldimethylamineNSC 3138Acetic acid dimethylamideCBC 510337DTXSID5020499SK 7176Dimethylamid kyseliny octoveU-5954

数据库标识

CAS
127-19-5
PubChem CID
31374
DTXSID
DTXSID5020499
ChEMBL
CHEMBL11873
ChEBI
CHEBI:84254
UNII
JCV5VDB3HY
EC Number
204-826-4
Nikkaji
J2.517H

性质

结构计算性质

XLogP
-0.8
极性表面积
20.3 Ų
氢键供体
0
氢键受体
1
可旋转键
0
重原子
6

实验与物化性质

LogP · 2 条

log Kow= -0.77

-0.77

Odor · 2 条

AMINE

Weak, ammonia- or fish-like odor

Density · 6 条

0.943 at 68 °F (USCG, 1999) - Less dense than water; will float

0.937 (USCG, 1999) - Less dense than water; will float

0.9366 @ 25 °C/4 °C

Relative density (water = 1): 0.94

0.94

0.943 @ 20°C

Viscosity0.92 cP @ 25 °C
Color/Form · 3 条

Liquid

OILY

Colorless liquid

Solubility · 6 条

greater than or equal to 100 mg/mL at 72 °F (NTP, 1992)

SOL IN BENZENE

Soluble in alcohol, acetone, ether

Miscible with most org solvents

MISCIBLE WITH AROMATIC CMPD, ESTERS, KETONES, ETHERS

Miscible in water.

物理化学性质

熔点
-20 °C · -20 °C (lit.)
沸点
164.5 · 164.5-166 °C (lit.)
密度
0.937 g/mL · 0.937 g/mL at 25 °C (lit.)
蒸气密度
3.89 · 3.89 (vs air)
蒸气压
40 mm · 40 mm Hg ( 19.4 °C)
折射率
20 · n20/D 1.439(lit.)

化学性质

无色透明液体。 能与水、醇、醚、酯、苯、三氯甲烷和芳香化合物等有机溶剂任意混合。

安全与法规

GHS分类

GHS Classification · 6 条

Danger

H312: Harmful in contact with skin [Warning Acute toxicity, dermal];H332: Harmful if inhaled [Warning Acute toxicity, inhalation];H360D ***: May damage the unborn child [Danger Reproductive toxicity]

P203, P261, P271, P280, P302+P352, P304+P340, P317, P318, P321, P362+P364, P405, and P501 (click each P-code to see the statement)

Danger

危害信息

Regulatory Information · 6 条

Chemical: Acetamide, N,N-dimethyl-

Hazard Traits - Carcinogenicity; Developmental Toxicity; Reproductive Toxicity;Authoritative List - EC Annex VI CMRs - Cat. 1B; IARC Carcinogens - 2B; Prop 65;Report - regardless of intended function of ingredient in the product

Acetamide, N,N-dimethyl- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Acetamide, N,N-dimethyl- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

Status: Active Update: 20-12-2022 https://echa.europa.eu/registration-dossier/-/registered-dossier/15266

Restricted substance: N,N-dimethylacetamide (DMAC);EC: 204-826-4;Restriction condition document: PDF link

Substance: N,N-dimethylacetamide;EC: 204-826-4;Date of inclusion: >19-Dec-2011;Reason for inclusion: Toxic for reproduction (Article 57c)

Other Safety InformationIMAP assessments - Acetamide, N,N-dimethyl-: Human health tier II assessment;IMAP assessments - Acetamide, N,N-dimethyl-: Environment tier I assessment
DOT Label · 2 条

Combustible Liquid

Poison

Fire Hazards · 3 条

This chemical is combustible. (NTP, 1992)

Special Hazards of Combustion Products: Emits carbon oxides, nitrogen oxides, and dimethylamine when heated to decomposition.;Behavior in Fire: Sealed closed containers may rupture from pressure from heat of fire. (USCG, 1999)

Combustible. Gives off irritating or toxic fumes (or gases) in a fire. Above 63 °C explosive vapour/air mixtures may be formed.

Fire PotentialCombustible when exposed to heat or flame.
Health Hazards · 2 条

Liquid causes mild irritation of eyes and skin. Ingestion causes depression, lethargy, confusion and disorientation, visual and auditory hallucinations, perceptual distortions, delusions, emotional detachment, and affective blunting. (USCG, 1999)

Inhalation may cause nasal and respiratory irritation. May cause systemic poisoning. Ingestion may cause abdominal spasms, vomiting, sweating, weakness, and headache. Large doses may cause lethargy, disorientation, redness, dermatitis, and sensitization. (USCG, 1999)

安全与防护

Fire Fighting · 3 条

Excerpt from ERG Guide 128 [Flammable Liquids (Water-Immiscible)]:;CAUTION: The majority of these products have a very low flash point. Use of water spray when fighting fire may be inefficient. CAUTION: For mixtures containing alcohol or polar solvent, alcohol-resistant foam may be more effective.;SMALL FIRE: Dry chemical, CO2, water spray or regular foam. If regular foam is ineffective or unavailable, use alcohol-resistant foam.;LARGE FIRE: Water spray, fog or regular foam. If regular foam is ineffective or unavailable, use alcohol-resistant foam. Avoid aiming straight or solid streams directly onto the product. If it can be done safely, move undamaged containers away from the area around the fire.;FIRE INVOLVING TANKS, RAIL TANK CARS OR HIGHWAY TANKS: Fight fire from maximum distance or use unmanned master stream devices or monitor nozzles. Cool containers with flooding quantities of water until well after fire is out. For petroleum crude oil, do not spray water directly into a breached tank car. This can lead to a dangerous boil over. Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank. ALWAYS stay away from tanks in direct contact with flames. For massive fire, use unmanned master stream devices or monitor nozzles; if this is impossible, withdraw from area and let fire burn. (ERG, 2024)

Fire Extinguishing Agents Not to Be Used: Do not use halogenated extinguishing media or water.;Fire Extinguishing Agents: Dry chemical, alcohol foam, carbon dioxide (USCG, 1999)

Use powder, alcohol-resistant foam, water spray, carbon dioxide.

First Aid Measures · 4 条

Fresh air, rest. Refer for medical attention.

Remove contaminated clothes. Rinse and then wash skin with water and soap. Refer for medical attention .

First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.

Rinse mouth. Give one or two glasses of water to drink. Do NOT induce vomiting. Seek medical attention if you feel unwell.

First Aid · 3 条

EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.;SKIN: IMMEDIATELY flood affected skin with water while removing and isolating all contaminated clothing. Gently wash all affected skin areas thoroughly with soap and water. If symptoms such as redness or irritation develop, IMMEDIATELY call a physician and be prepared to transport the victim to a hospital for treatment.;INHALATION: IMMEDIATELY leave the contaminated area; take deep breaths of fresh air. If symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop, call a physician and be prepared to transport the victim to a hospital. Provide proper respiratory protection to rescuers entering an unknown atmosphere. Whenever possible, Self-Contained Breathing Apparatus (SCBA) should be used; if not available, use a level of protection greater than or equal to that advised under Protective Clothing.;INGESTION: DO NOT INDUCE VOMITING. If the victim is conscious and not convulsing, give 1 or 2 glasses of water to dilute the chemical and IMMEDIATELY call a hospital or poison control center. Be prepared to transport the victim to a hospital if advised by a physician. If the victim is convulsing or unconscious, do not give anything by mouth, ensure that the victim's airway is open and lay the victim on his/her side with the head lower than the body. DO NOT INDUCE VOMITING. IMMEDIATELY transport the victim to a hospital. (NTP, 1992)

Call for medical aid.;EYES: Flush with plenty of water for 15 min., lifting lids occasionally.;SKIN: Flush with plenty of water for 15 min. Remove contaminated clothing and shoes.;INGESTION: Induce vomiting. (USCG, 1999)

(General first aid procedures);Eye: Irrigate immediately - If this chemical contacts the eyes, immediately wash (irrigate) the eyes with large amounts of water, occasionally lifting the lower and upper lids. Get medical attention immediately.;Skin: Water flush immediately - If this chemical contacts the skin, immediately flush the contaminated skin with water. If this chemical penetrates the clothing, immediately remove the clothing and flush the skin with water. Get medical attention promptly.;Breathing: Respiratory support;Swallow: Medical attention immediately - If this chemical has been swallowed, get medical attention immediately.

Safe StorageVentilation along the floor. Separated from strong oxidants.
Exposure Control and Personal Protection · 2 条

Biological Exposure Indices (BEI) [ACGIH] - M-Methylacetamide in urine = 30 mg/g creatinine; end of shift at end of workweek;

5.0 [ppm]

Fire Fighting ProceduresEXTINGUISH WITH WATER, DRY CHEMICALS, ALCOHOL FOAM OR CARBON DIOXIDE

毒理信息

Body BurdenN,N-dimethylacetamide was qualitatively found in 8 of 12 breath samples of subjects monitored in Bayonne and Elizabeth, NJ, and Research Triangle Park, NC, 1980(1).
Interactions · 4 条

DAILY INJECTIONS OF PROGESTERONE (5 MG/HAMSTER/DAY, FOR 4 DAYS) BLOCKED ANTIFERTILITY EFFECT OF DMA (ADMIN @ NIDATION) AS DID INJECTIONS OF A LUTEOTROPIC COMPLEX (1 MG/HAMSTER/DAY PROLACTIN PLUS 5.1 IU/HAMSTER/DAY OF PREGNANT MARE SERUM GONADOTROPIN, FOR 4 DAYS.

DIMETHYLACETAMIDE LOWERED THE YIELDS AND/OR INCIDENCES OF TOTAL TUMORS, BENIGN PLAQUES, BENIGN HYPERKERATOTIC LESIONS AND ADVANCED TUMORS PROMOTED BY RETINYL ACETATE OR CROTON OIL AFTER INITIATION BY 7,12-DIMETHYLBENZ(A)ANTHRACENE.

SINGLE EXPT WITH 45 MG/KG RAT OF PYRIMETHAMINE ISETHIONATE IN 6% DIMETHYLACETAMIDE, 6% DIMETHYL SULFOXIDE OR 95% ETHANOL SHOWED THAT TERATOGENIC EFFECT WAS CUMULATIVE IN DIMETHYL SULFOXIDE OR ETHANOL BUT AFTER ADMIN IN DMA RESPONSE-DOSE RELATION FOLLOWED A PARABOLIC CURVE.

PCC4azal embryonal carcinoma tumors were grown in strain 129 mice by sc transplantation. When palpable, the tumors were treated with a combination of retinoic acid and dimethylacetamide. In vitro, this embryonal carcinoma cell line shows minimal spontaneous differentiation and is exquistely sensitive to retinoic acid and/or dimethylacetamide induction of differentiation. Ten daily 20 ul intratumor injections of a solution of 10 mg retinoic acid per ml of dimethylacetamide resulted in nearly complete induction of morphological differentiation mainly into neuropithelial and glandular derivatives. Control tumors showed minor spontaneous differentiation. Differentiation was associated with decreased tumor growth rate, decreased mitotic index, decreased extent of necrosis, and increased survival time of the hosts. In 4 of 18 cases, long-term survival of the hosts was effected by a complete differentiation of the malignant embryonal carcinoma tumors into benign teratomas. Retinoic acid: dimethylacetamide was also effective in inducing differentiation with the same dosage and schedule when admin systemically, ie, ip or sc.

Target OrgansSkin, liver, central nervous system
Ecotoxicity Values · 1 条

LC50 Pimephales promelas (fathead minnow) 1.50 g/l/96 hr (confidence limit 1.21- 1.86 g/l), flow-through bioassay with measured concentrations, 23.1 °C, dissolved oxygen 6.6 mg/l, hardness 45.0 mg/l calcium carbonate, alkalinity 43.5 mg/l calcium carbonate, and pH 7.7.

Environmental Fate · 3 条

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 9(SRC), determined from a log Kow of -0.77(2) and a regression-derived equation(3), indicates that N,N-dimethylacetamide is expected to have very high mobility in soil(SRC). Volatilization of N,N-dimethylacetamide from moist soil surfaces is not expected to be an important fate process(SRC) given a Henry's Law constant of 1.31X10-8 atm-cu m/mole(4). The potential for volatilization of N,N-dimethylacetamide from dry soil surfaces may exist(SRC) based upon a vapor pressure of 2 mm Hg(5). N,N-Dimethylacetamide is expected to be biodegradable in soil based on aqueous screening tests(6,7).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 9(SRC), determined from a log Kow of -0.77(2) and a regression-derived equation(3), indicates that N,N- dimethylacetamide is not expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is not expected(3) based upon a Henry's Law constant of 1.31X10-8 atm-cu m/mole(4). According to a classification scheme(5), an estimated BCF of 3(SRC), from its log Kow(2) and a regression-derived equation(6), suggests the potential for bioconcentration in aquatic organisms is low(SRC). N,N-Dimethylacetamide, present at 100 mg/l reached 28% of its theoretical BOD in 4 weeks using an activated sludge inoculum at 30 mg/l and the Japanese MITI test(7). N,N-Dimethylacetamide, present at 30 mg/l, reached 80% of its theoretical BOD in 4 weeks using an activated sludge inoculum at 100 mg/l and the Japanese MITI test(7). In other studies, N,N-dimethylacetamide, present at 400 mg/l, reached 96% of its theoretical TOC in 5 days using industrial activated sludge(8). These results from laboratory studies suggest that N,N-dimethylacetamide will biodegrade in the aquatic environment(SRC).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), N,N-dimethylacetamide, which has a vapor pressure of 2 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere(SRC). Vapor-phase N,N-dimethylacetamide is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is 28 hours(SRC), calculated from its rate constant of 1.36X10-11 cu cm/molecule-sec at 25 °C(3).

Adverse Effects · 1 条

Neurotoxin - Acute solvent syndrome;Occupational hepatotoxin - Primary hepatotoxins: the toxic effect to the liver is the principal adverse effect of the chemical.;Nephrotoxin - The chemical is potentially toxic to the kidneys in the occupational setting.;Reproductive Toxin - A chemical that is toxic to the reproductive system, including defects in the progeny and injury to male or female reproductive function. Reproductive toxicity includes developmental effects. See Guidelines for Reproductive Toxicity Risk Assessment.;IARC Carcinogen - Class 3: Chemicals are not classifiable by the International Agency for Research on Cancer.;ACGIH Carcinogen - Confirmed Animal.

法规信息

Regulatory Information · 6 条

Chemical: Acetamide, N,N-dimethyl-

Hazard Traits - Carcinogenicity; Developmental Toxicity; Reproductive Toxicity;Authoritative List - EC Annex VI CMRs - Cat. 1B; IARC Carcinogens - 2B; Prop 65;Report - regardless of intended function of ingredient in the product

Acetamide, N,N-dimethyl- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Acetamide, N,N-dimethyl- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

Status: Active Update: 20-12-2022 https://echa.europa.eu/registration-dossier/-/registered-dossier/15266

Restricted substance: N,N-dimethylacetamide (DMAC);EC: 204-826-4;Restriction condition document: PDF link

Substance: N,N-dimethylacetamide;EC: 204-826-4;Date of inclusion: >19-Dec-2011;Reason for inclusion: Toxic for reproduction (Article 57c)

TSCA Requirements · 2 条

Section 8(a) of TSCA requires manufacturers of this chemical substance to report preliminary assessment information concerned with production, use, and exposure to EPA as cited in the preamble in 51 FR 41329.

Pursuant to section 8(d) of TSCA, EPA promulgated a model Health and Safety Data Reporting Rule. The section 8(d) model rule requires manufacturers, importers, and processors of listed chemical substances and mixtures to submit to EPA copies and lists of unpublished health and safety studies. N,N-Dimethylacetamide is included on this list.

安全数据

F
3-10
wgk
WGK 2
tsca
TSCA listed
毒性
LD50 orally in rats: 5.4 ml/kg (Bartsch)
RTECS号
AB7700000
存储类别
6.1C - Combustible acute toxic Cat.3toxic compounds or compounds which causing chronic effects
毒性防护 · 3 条

急性毒性口服- 大鼠 LD50: 4300 毫克/ 公斤; 口服- 小鼠 LD50: 4620 毫克/ 公斤

刺激数据皮肤- 兔子 10 毫克/ 24小时 轻度; 眼- 兔子 100 毫克 轻度

职业标准TLV-TWA 10 PPM (35 毫克/ 立方米); STEL 15 PPM (50 毫克/ 立方米)

包装储运 · 4 条

爆炸物危险特性与空气混合可爆

可燃性危险特性遇明火、高温、强氧化剂可燃; 燃烧排放有毒氮氧化物烟雾

储运特性包装完整、轻装轻卸; 库房通风、远离明火、高温、与氧化剂、酸分开存放

灭火剂泡沫、干粉、二氧化碳

化学与工业

药理信息

Metabolism/Metabolites · 4 条

N-DEMETHYLATION OF ... DIMETHYLACETAMIDE OCCURRED IN RAT, RESPECTIVE MONOMETHYLAMIDES APPEARING IN URINE ... IN THE CASE OF DIMETHYLACETAMIDE WAS DIDEMETHYLATED PRODUCT, ACETAMIDE, ALSO FOUND.

ANALYSIS OF HUMAN URINE AFTER OCCUPATIONAL EXPOSURE TO DIMETHYLACETAMIDE SHOWS N-METHYLACETAMINE. /FROM TABLE/

Gas chromatographic analysis of the urine of rats which had received dimethylacetamide by the subcutaneous route indicated the presence of N-methyl-acetamide and acetamide. Both metabolites were also found ... in incubation mixtures of dimethylacetamide with rat liver homogenate. N-Methylacetamide was detected in the urine of human volunteers who had inhaled dimethylacetamide or absorbed dimethylacetamide vapor through the skin. Measurement of the amount of the metabolite N-methylacetamide excreted by individuals exposed to dimethylacetamide vapors with or without face masks which allowed the inhalation of air free of dimethylacetamide indicated that more dimethylacetamide was absorbed through the lung than through the skin. ... Only 2-10% of the amount of dimethylacetamide inhaled was recovered in the urine in the form of N-methylacetamide. It has been suggested that the major urinary metabolite of the analogous dimethylformamide is N-(hydroxymethyl)-N-methylformamide and not N-methylformamide, since the carbinolamide decomposes on the gas chromatography column (to N-methylformamide) but is relatively stable in aqueous solution. In analogy, it would be logical to assume that the N-methylacetamide found in the urine after exposure to dimethylacetamide really arose from chemical breakdown of N-(hydroxymethyl)-N-methylacetamide during the analytical process.

N,N-dimethylacetamide is metabolized by demethylation first to monomethyl derivatives and then to the parent acetamide.

MeSH Pharmacological ClassificationSubstances that provide protection against the harmful effects of freezing temperatures.
Absorption, Distribution and Excretion · 5 条

/N,N-DIMETHYLACETAMIDE/ ... READILY ABSORBED THROUGH SKIN ... .

N,N-dimethylacetamide is rapidly absorbed through biological membranes.

No correlation between personal airborne exposure and excretion of mono-methylacetamide in urine was detected during a full workshift (5 days). Most (n = 6) workers studied (n = 8) excreted about 13% of the calculated inhaled dose as metabolite in urine.

DMAC is readily absorbed in man after oral, dermal, or inhalation exposure. ... About 2% of a dose of dimethylacetamide is recovered in the urine as MMAC /N-methylacetamide/ after inhalation; 10% is recovered after inhalation plus skin exposure. Exposure to 10 ppm of DMAC results in complete excretion of MMAC with in 30 hr. Maximal concns of 45 & 100 ppm (mg/L) of MMAC in the urine are found in subjects exposed both by inhalation & skin. In workers continuously exposed to DMAC vapor (inhalation plus skin) & subjected to DMAC airborne levels of 6-22 ppm ..., about 13.5% of the estimated dose is excreted as MMAC in the urine. Some workers may excrete about 30% of a dose as MMAC.

For more Absorption, Distribution and Excretion (Complete) data for N,N-DIMETHYLACETAMIDE (7 total), please visit the HSDB record page.

用途与制造

Uses · 6 条

Used as a solvent for many organic reactions, resins, polymers, crystallization, and purification. [ACGIH] Used as a solvent in plastics, resins, and gums; Also used as a catalyst and paint remover; [Hawley] Used in synthetic fiber and resin industries; Used as a solvent in elastane fiber factories; [Reference #1]

Semiconductor Manufacturing [Category: Industry];Plastic Composites Manufacturing [Category: Industry]

Solvent in industrial applications

Solvent for plastics, resins, gums, and electrolytes; catalyst; paint remover; high-purity solvent for crystallization and purification

N,N-Dimethylacetamide is used to dissolve polyacrylonitrile, polyvinyl chloride, polyamides, polyimides, cellulose derivatives, styrenes, and linear polyesters; manufacturing of films and fibers; booster solvent in coatings and adhesives formulations.

Electrolytic solvent; formation of dimethylacetamide complexes; chemical reaction medium and catalyst

U.S. Production · 2 条

2023: 25,000,000 - <40,000,000 lb;2022: 70,000,000 - <85,000,000 lb;2021: 70,000,000 - <85,000,000 lb;2020: 55,000,000 - <70,000,000 lb

(1972) GREATER THAN 4.54X10+5 GRAMS

Consumer UsesSemiconductor and photovoltaic agent;Solvent;Intermediate;Not Known or Reasonably Ascertainable
Industry UsesNot Known or Reasonably Ascertainable;Soil amendments (fertilizers);Laboratory chemicals;Intermediate;Binder;Solvent;Fuel agents;Semiconductor and photovoltaic agent
Methods of Manufacturing · 4 条

From tris(dimethylamido)phosphate and acetic anhydride. From acetic anhydride and dimethylformamide.

By reaction of acetic acid and dimethylamine.

Reaction of methyl acetate and dimethylamine; reaction of dimethylamine with the azotrope of methyl acetate and methanol.

Reaction of N,N-dimethylamine and acetic anhydride.

Formulations/PreparationsGrades: ... high purity certified.
应用领域 · 5 条

概述N,N-二甲基乙酰胺又称乙酰基二甲胺、乙酰二甲胺,简称DMAC,是一种非质子高极性溶剂,有微氨气味,溶解力很强,可溶解的物质范围很广,能与水、芳香族化合物、酯、酮、醇、醚、苯和三氯甲烷等任意混溶,且能使化合物分子活化,因此广泛用作溶剂及催化剂。在溶剂方面作为高沸点、高闪点、热稳定性高、化学性稳定的溶剂,可用于聚丙烯腈的抽丝溶剂、合成树脂及天然树脂、甲酸乙烯酯、乙烯基吡啶等共聚物及芳烃羧酸的溶剂;在催化剂方面可用于尿素加热制氰尿酸、卤代烷与金属氰化物反应制腈、乙炔钠与卤代烷反应制烷基炔、有机卤化物与氰酸盐反应制异氰酸酯等过程。N,N-二甲基乙酰胺还可用作电解溶剂及摄影用成色剂的溶剂、脱油漆剂、有机合成原料、农药及医药原料。从C8馏分中分离苯乙烯的萃取蒸馏溶剂等。

用途用作合成纤维的原料及有机合成的优良极性溶剂

用途用于有机合成,也用作溶剂、催化剂和去漆剂

用途DMAC主要用作合成纤维(丙烯腈)和聚氨酯纺丝及合成聚酰胺树脂的溶剂,也用于从C8馏分分离苯乙稀的萃取蒸馏溶剂,并广泛用于高分子薄膜、涂料和医药等方面。目前在医药和农药上大量用来合成抗菌素和农药杀虫剂。还可用作反应的催化剂、电解溶剂、油漆清除剂以及多种结晶性的溶剂加合物和络合物。

用途用于药物合成的反应溶剂,合成纤维纺丝与合成树脂的溶剂,感光化学品发色剂的溶剂,涂料等的溶剂。催化剂。

制备方法 · 1 条

生产方法1.乙酐法二甲胺与醋酐在0-20℃时进行酰化反应,然后用液碱低温中和除去醋酸,分离出醋酸钠,中和液再进行碱洗,精馏,取沸程164-166.5℃馏分为成品。原料消耗定额:乙酐(95%)1150kg/t、二甲胺(40%)1898kg/t。2.乙酰氯法由二甲胺与乙酰氯反应,也可制备得到二甲基乙酰胺。该工艺与国内现行乙酐法工艺相比,生产成本降低,经济效益有所提高。3.醋酸法抚顺市化工设备研究院采用醋酸与二甲胺合成法,取得了良好成果。该工艺特点是采用先进的催化反应精馏技术,使反应强化,能耗降低,分离效果和产品收率大大提高,工艺过程简化。该工艺与醋酐法合成二甲基乙酰胺工艺相比,生产成本降低,经济效益有所提高。中国目前多用。4.羰基合成法国外研究将三甲胺和一氧化碳进行羰基化合成,生成N,N-二甲基乙酰胺的方法。反应中用铁、钴、镍的碘化物或溴化物作催化剂。

试剂价格

HY-W042416R · 50 mg
N,N-二甲基乙酰胺N,N-Dimethylacetamide (Standard) — 330元
XW01271956 · 1L
N,N-二甲基乙酰胺n,n-dimethylacetamide;n-acetyldimethylamine;dma — 402元

供应商50 家

国药集团化学试剂有限公司86-21-63210123 · [email protected]
梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
衢州润东化工有限公司0570-8789886 18892685668 · [email protected]
山东旭晨化工科技有限公司0533-15715337262 15715337262 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]

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