Synthesis
ChemicalBook > CAS DataBase List > Acetamide

Acetamide

Synthesis
Product Name
Acetamide
CAS No.
60-35-5
Chemical Name
Acetamide
Synonyms
CH3CONH2;Acetamid;ETHANAMIDE;AMIDE C2;Actamide;ACETAMIDE;Acetamidum;NCI-C02108;Acetylamide;acetylamine
CBNumber
CB3453432
Molecular Formula
C2H5NO
Formula Weight
59.07
MOL File
60-35-5.mol
More
Less

Acetamide Property

Melting point:
78-80 °C(lit.)
Boiling point:
221 °C(lit.)
Density 
1.159
vapor pressure 
1 mm Hg ( 65 °C)
refractive index 
1.4274
Flash point:
220-222°C
storage temp. 
Store below +30°C.
solubility 
H2O: 0.5 g/mL, Hazen ≤50
pka
0.63(at 25℃)
form 
Crystals
color 
White
Odor
Mousy odor
Water Solubility 
2000 g/L (20 ºC)
Merck 
14,43
JECFA Number
1592
BRN 
1071207
Dielectric constant
41.0(20℃)
Exposure limits
ACGIH: TWA 1 ppm
Stability:
Stable. Incompatible with strong acids, strong oxidizing agents, strong bases. Deliquescent. Triboluminescent.
InChIKey
DLFVBJFMPXGRIB-UHFFFAOYSA-N
LogP
-1.26
CAS DataBase Reference
60-35-5(CAS DataBase Reference)
NIST Chemistry Reference
Acetamide(60-35-5)
IARC
2B (Vol. 7, Sup 7, 71) 1999
EPA Substance Registry System
Acetamide (60-35-5)
More
Less

Safety

Hazard Codes 
Xn
Risk Statements 
40
Safety Statements 
36/37
RIDADR 
UN 3077 9/PG 3
WGK Germany 
1
RTECS 
AB4025000
3
Autoignition Temperature
560°C
TSCA 
Yes
HS Code 
29241900
Hazardous Substances Data
60-35-5(Hazardous Substances Data)
Toxicity
LD50 orally in Rabbit: 7000 mg/kg
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H351Suspected of causing cancer

Precautionary statements

P201Obtain special instructions before use.

P202Do not handle until all safety precautions have been read and understood.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P308+P313IF exposed or concerned: Get medical advice/attention.

P405Store locked up.

P501Dispose of contents/container to..…

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
8.22343
Product name
Acetamide
Purity
for synthesis
Packaging
100g
Price
$48.9
Updated
2024/03/01
Sigma-Aldrich
Product number
8.22343
Product name
Acetamide
Purity
for synthesis
Packaging
1kg
Price
$153
Updated
2024/03/01
Sigma-Aldrich
Product number
00160
Product name
Acetamide
Purity
≥99.0% (GC)
Packaging
50g
Price
$33.6
Updated
2024/03/01
Sigma-Aldrich
Product number
00160
Product name
Acetamide
Purity
≥99.0% (GC)
Packaging
1kg
Price
$224
Updated
2024/03/01
TCI Chemical
Product number
A0007
Product name
Acetamide
Purity
>98.0%(GC)
Packaging
25g
Price
$34
Updated
2024/03/01
More
Less

Acetamide Chemical Properties,Usage,Production

Synthesis

Laboratory synthesis can be carried out according to the following steps. Put 3kg glacial acetic acid into a 5L flask and add ammonium carbonate equivalent to 400g ammonia. The flask is equipped with a high-efficiency fractionation column, a condenser and a receiver. Heat the reaction mixture until it boils slowly, adjust the heating so that the distillation rate does not exceed 180mg / h until the top temperature reaches 110 ℃. A mixture of 1400-1500 ml of water and acetic acid was obtained. Change the receiver, slowly increase the heating, and continue the distillation at the same speed until the top temperature rises to 140 ℃. The distillate is 500-700ml, mainly acetic acid, which is reserved for the next feeding. Transfer the residue into a flask with fractionation column and air condenser, distill under normal pressure, and collect the fractions before 210 ℃ and 210-216 ℃ respectively. The latter is acetamide, weighing 1150-1200g. The former can also distill and recover some products. The total weight of the two is 1200-1250g, and the yield is 87% - 90%.
The recrystallization of acetylamine is usually carried out by distillation and solvent recrystallization. The commonly used solvents are acetone, benzene, ethyl acetate, methyl acetate, chloroform, dioxane or the mixture of benzene and ethyl acetate. For example, 1kg of acetamide prepared by the above method is recrystallized with a mixed solvent of 1l benzene and 300ml ethyl acetate to obtain a colorless needle like pure product. The purity of products obtained from industrial production shall not be lower than 98%, and the freezing point shall not be lower than 76 ℃.

Description

Acetamide (MEA or ethanamide), the amide of acetic acid, is a white crystalline solid in pure form with a mousy odor. Low toxicity. It is produced by dehydrating ammonium acetate. Acetamide is found in red beetroot.
Acetamide is used primarily as a solvent, plasticizer, and a wetting and penetrating agent. it was used as an intermediate in the synthesis of methylamine, thioacetamide, hypnotics, insecticides, medicinals and various plastics, a soldering flux ingredient, a wetting agent and penetration accelerator for dyes, and as a plasticizer in leather, cloth and coatings.
ethanolamine is an amide made from acetamide and monoethanolamine. It is a clear liquid. In cosmetics and personal care products, It is used in the formulation of bubble baths, hair conditioners, shampoos, wave sets, moisturizers, and other bath and hair care products.It increases the water content of the top layers of the skin by drawing moisture from the surrounding air. It also enhances the appearance and feel of hair, by increasing hair body, suppleness, or sheen, or by improving the texture of hair that has been damaged physically or by chemical treatment.

Chemical Properties

Acetamide occurs as hexagonal colourless deliquescent crystals with a musty odour. It is incompatible with strong acids, strong oxidising agents, strong bases, and triboluminescent materials. Acetamide is used primarily as a solvent, a plasticiser, and a wetting and penetrating agent. Workplace exposures to acetamide are associated with the plastic and chemical industries.

Chemical Properties

Acetamide is a colorless to yellow, deliquescent, crystalline solid. Odorless if pure, “mousy” odor if impure. Odor threshold5140 160 milligram per cubic meter.

Uses

Cryoscopy; organic synthesis; general solvent; lacquers; explosives, soldering flux; wetting agent; plasticizer

Uses

As a dipolar solvent, acetamide finds many uses as a solvent for both inorganic and organic compounds. The solvency has led to widespread uses in industry including applications in cryoscopy, soldering, and the textile industry. The neutral and amphoteric characteristics allow its use as an antacid in the lacquer, explosives, and cosmetics industries. Its hygroscopic properties make it useful as a plasticizer in coatings, fixtures, cloth, and leather, and as a humectant for paper. It is also a raw material in organic synthesis of methylamine and thioacetamide and as an intermediate in preparation of medicines, insecticides, and plastics.

Uses

  1. Acetamide is often used as plasticizer and as industrial solvent.
  2. molten acetamide is an excellent solvent for many organic and inorganic compounds.
  3. Solubilizer.
  4. renders sparingly soluble substances more soluble in water by mere addition or by fusion.
  5. stabilizer.
  6. manufacture of methylamine, denaturing alcohol.
  7. In organic syntheses.
  8. Acetamide is used as a co-monomer in the production of polymeric materials such as polyvinyl acetamide, a polymeric product used as an absorbent.
  9. It can be used for the transamidation of carbxamides in 1,4-dioxane in the absence of a catalyst.

Definition

ChEBI: Acetamide is a member of the class of acetamides that results from the formal condensation of acetic acid with ammonia. It is a monocarboxylic acid amide, a N-acylammonia and a member of acetamides. It is a tautomer of an acetimidic acid.

General Description

Colorless crystals with a mousy odor (NTP, 1999). Low toxicity.

Air & Water Reactions

Deliquescent. Very soluble in water.

Reactivity Profile

Acetamide may react with azo and diazo compounds to generate toxic gases. May form flammable gases with strong reducing agents. Reacts as a weak bases (weaker than water). Mixing with dehydrating agents such as P2O5 or SOCl2 generates acetonitrile Burns to give toxic mixed oxides of nitrogen (NOx).

Health Hazard

After oral exposures to acetamide, animals developed liver tumors. However, no informa- tion is available on the carcinogenic effects of acetamide in humans. The US EPA has not classifi ed acetamide for carcinogenicity. The IARC has classifi ed acetamide as a Group 2B, meaning a possible human carcinogen.

Health Hazard

Mild irritant; acute oral toxicity in animals very low; oral LD50 value (rats):7000 mg/kg; carcinogenic to animals; oraladministration caused blood and liver tumorsin mice and rats; carcinogenicity: animal limited evidence, no evidence in humans.

Fire Hazard

The flash point of Acetamide has not been determined, but Acetamide is probably combustible.

Safety Profile

Suspected carcinogen with experimental carcinogenic and neoplastigenic data. Moderately toxic by intraperitoneal and possibly other routes. An experimental teratogen. Other experimental reproductive effects. Mutation data reported. See also AMIDES. When heated to decomposition it emits toxic fumes of NOx,.

Potential Exposure

Used as a stabilizer, plasticizer, wetting agent; solvent in plastics, lacquers, explosive; soldering flux ingredient; and chemical manufacturing

target

Histone Methyltransferase

Carcinogenicity

The IARC has determined that there is sufficient evidence of carcinogenicity for acetamide in experimental animals and that it is possibly carcinogenic to humans.

Environmental Fate

The mechanism of toxicity of acetamide is not known; the response profile is quite different from the better studied dimethyl derivative. Acetamide appears to be in a class of chemicals which, although producing liver cancer in rodents, is less sensitive to inactive in genetic tests looking at formation of micronuclei. The carcinogenic response in rodents appears related to the formation of hydroxylamine from the primary metabolite acetohydroxamic acid.

storage

Acetamide should be kept stored in a tightly closed container, in a cool, dry, ventilated area. It should be protected against physical damage, away from any source of heat, ignition, or oxidizing materials.

Shipping

UN3077 Environmentally hazardous substances, solid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous material, Technical Name Required

Purification Methods

Acetamide is crystallised by dissolving in hot MeOH (0.8mL/g), diluting with Et2O and allowing to stand [Wagner J Chem Edu 7 1135 1930]. Alternate crystallisation solvents are acetone, *benzene, chloroform, dioxane, methyl acetate or *benzene/ethyl acetate mixtures (3:1 and 1:1). It has also been recrystallised from hot water after treating with HCl-washed activated charcoal (which had been repeatedly washed with water until free from chloride ions), then crystallised again from hot 50% aqueous EtOH and finally twice from hot 95% EtOH [Christoffers & Kegeles J Am Chem Soc 85 2562 1963]. Finally it is dried in a vacuum desiccator over P2O5. Acetamide is also purified by distillation (b 221-223o) or by sublimation in vacuo. It has also been purified by two recrystallisations from cyclohexane containing 5% (v/v) of *benzene. Needle-like crystals separate and are filtered, washed with a small volume of distilled H2O and dried with a flow of dry N2. [Slebocka-Tilk et al. J Am Chem Soc 109 4620 1987, Beilstein 2 H 175, 2 I 80, 2 II 177, 2 III 384, 2 IV 399.]

Toxicity evaluation

Acetamide will exist as a vapor in the ambient atmosphere. Atmospheric degradation occurs by reaction with photochemically produced hydroxyl radicals. The half-life for this reaction in air is estimated to be 7.6 days. If released to soil, acetamide is expected to have very high mobility and is not expected to adsorb to suspended solids and sediment. Experiments suggest that this chemical may break down in the environment through biodegradation and not through hydrolysis. Volatilization from water surfaces is not expected to be an important fate process based on this compound’s estimated Henry’s law constant.

Incompatibilities

Reacts with strong acids, such as hydrochloric, sulfuric, and nitric, strong oxidizers; strong bases; strong reducing agents such as hydrides; ammoniaisocyanates, phenols, cresols. Contact with water causes slow hydrolyzation to ammonia and acetate salts.

Waste Disposal

Add to alcohol or benzene as a flammable solvent and incinerate; oxides of nitrogen produced may be scrubbed out with alkaline solution. All federal, state, and local environmental regulations must be observed.

Precautions

During handling and/use of acetamide, workers should wear special protective equipment. After leaving work areas, workers should wash hands, face, forearms, and neck, dispose of outer clothing, and change to clean garments at the end of the day.

More
Less

Acetamide Suppliers

Guizhou Dida Technology Co., Ltd
Tel
0851-8475-2296 18096062265
Fax
0851-84752205
Email
646585516@qq.com
Country
China
ProdList
2779
Advantage
58
Shanghai hongrui chemical co., ltd
Tel
13906273813 13485185589
Email
834955168@qq.com
Country
China
ProdList
35
Advantage
58
JinJin Le Chemical Co., Ltd
Tel
10106090
Email
jjlchem2@163.com
Country
China
ProdList
9986
Advantage
58
Unichem Company Ltd.(China)
Tel
0510-0510-82328705 13771137389
Fax
86-510-82328706
Email
webmaster@unionchems.com
Country
China
ProdList
28
Advantage
58
shanghaidelaikekejiyouxiangongsi
Tel
17351445187
Email
3528434302@qq.com
Country
China
ProdList
282
Advantage
58
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
94838
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006608290; 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40241
Advantage
62
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Fax
86-21-50328109
Email
3bsc@sina.com
Country
China
ProdList
15848
Advantage
69
Chembest Research Laboratories Limited
Tel
021-20908456
Fax
021-58180499
Email
sales@BioChemBest.com
Country
China
ProdList
6011
Advantage
61
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30132
Advantage
84
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24539
Advantage
81
BeiJing Hwrk Chemicals Limted
Tel
0757-86329057 18501085097
Fax
010-89508210
Email
sales3.gd@hwrkchemical.com
Country
China
ProdList
7583
Advantage
55
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44751
Advantage
61
Beijing Ouhe Technology Co., Ltd
Tel
010-82967028 13552068683
Fax
+86-10-82967029
Email
2355560935@qq.com
Country
China
ProdList
12458
Advantage
60
Secco work (Beijing) chemical technology co., LTD
Tel
0566-8928158
Fax
010-69755668
Email
343367102@QQ.COM
Country
China
ProdList
360
Advantage
54
Accela ChemBio Co.,Ltd.
Tel
021-50795510 4000665055
Fax
021-50795055
Email
sales@accelachem.com
Country
China
ProdList
11660
Advantage
64
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696;
Email
info@hanhongsci.com
Country
China
ProdList
42982
Advantage
64
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
32344
Advantage
50
XiaoGan ShenYuan ChemPharm co,ltd
Tel
0712-0712-2580635 15527768850
Email
1791901229@qq.com
Country
China
ProdList
8849
Advantage
52
Shandong Xiya Chemical Co., Ltd
Tel
13355009207 13355009207
Fax
0539-6365991
Email
3007715519@qq.com
Country
China
ProdList
18739
Advantage
57
Syntechem Co.,Ltd
Tel
Fax
E-Mail Inquiry
Email
info@syntechem.com
Country
China
ProdList
12990
Advantage
57
BEST-REAGENT
Tel
400-1166-196 18981987031
Fax
028-84555506 800101999
Email
cdhxsj@163.com
Country
China
ProdList
11726
Advantage
57
China Langchem Inc.
Tel
0086-21-58956006
Fax
0086-21-58956100
Country
China
ProdList
7815
Advantage
57
Tianjin heowns Biochemical Technology Co., Ltd.
Tel
400 638 7771
Email
sales@heowns.com
Country
China
ProdList
14443
Advantage
57
Sinopharm Chemical Reagent Co,Ltd.
Tel
86-21-63210123
Fax
86-21-63290778 86-21-63218885
Email
sj_scrc@sinopharm.com
Country
China
ProdList
9823
Advantage
79
Maya High Purity Chemicals
Tel
+86 (573) 82222445 (0)18006601000 452520369
Fax
+86 (573) 82222643
Email
sales@maya-r.com
Country
China
ProdList
11714
Advantage
57
Spectrum Chemical Manufacturing Corp.
Tel
021-021-021-67601398-809-809-809 15221380277
Fax
021-57711696
Email
marketing_china@spectrumchemical.com
Country
China
ProdList
9664
Advantage
60
Wuhan Fortuna Chemical Co., Ltd
Tel
027-027-59207852 13308628970
Fax
QQ3130921841
Email
buy@fortunachem.com
Country
China
ProdList
2893
Advantage
58
BioBioPha Co., Ltd.
Tel
0871-65217109 13211707573;
Fax
0871-65215563
Email
y.liu@mail.biobiopha.com
Country
China
ProdList
5654
Advantage
65
Chengdu Ai Keda Chemical Technology Co., Ltd.
Tel
4008-755-333 18080918076
Fax
028-86757656
Email
800078821@qq.com
Country
China
ProdList
9725
Advantage
55
Shanghai civi chemical technology co.,Ltd
Tel
86-21-34053660
Fax
86-21-34053661
Email
sale@labgogo.com
Country
China
ProdList
9872
Advantage
52
Thermo Fisher Scientific
Tel
800-810-5118
Fax
+86-10-84193589
Email
cnchemical@thermofisher.com
Country
China
ProdList
17779
Advantage
75
Beijing HuaMeiHuLiBiological Chemical
Tel
010-56205725
Fax
010-65763397
Email
waley188@sohu.com
Country
China
ProdList
12338
Advantage
58
Beijing innoChem Science & Technology Co.,Ltd.
Tel
400-810-7969 010-59572699
Fax
010-59572688
Email
ningzi.li@inno-chem.com.cn
Country
China
ProdList
6139
Advantage
55
Yurui (Shanghai) Chemical Co., Ltd.
Tel
02150456736 13818239876
Fax
021-50761379
Email
xin@riyngroup.com
Country
China
ProdList
1136
Advantage
30
Shanghai Jian Chao Chemical Technology Co., Ltd.
Tel
021-50430803 18017383231
Fax
qq:2817624287
Email
983544897@qq.com
Country
China
ProdList
9352
Advantage
55
9ding chemical ( Shanghai) Limited
Tel
4009209199
Fax
86-021-52271987
Email
sales@9dingchem.com
Country
China
ProdList
22519
Advantage
55
Shanghai Aladdin Bio-Chem Technology Co.,LTD
Tel
18521735133 18521732826;
Fax
021-50323701
Email
market@aladdin-e.com
Country
China
ProdList
25015
Advantage
65
The future of Shanghai Industrial Co., Ltd.
Tel
021-61552785
Fax
021-55660885
Email
sales@shshiji.com
Country
China
ProdList
9552
Advantage
55
Shanghai Ruji Biology Technology Co., Ltd.
Tel
+86-21-65211385-8001 36031160
Fax
+86-21-65211385-8004
Email
sales@shruji.com
Country
China
ProdList
3224
Advantage
55
Chengdu AstaTech Trading Co., Ltd./AstaTech (Chengdu) Pharma. Co., Ltd.
Tel
+86-28-85122536 85324413
Fax
+86-28-85326443
Email
market@astatech.cn
Country
China
ProdList
8033
Advantage
55
Sinfachem Limited
Tel
025-84683399 13952017251
Fax
025-84683112
Email
sales@sinfachem.com
Country
China
ProdList
217
Advantage
56
Beijing Universal Century Technology Co., Ltd.
Tel
400-8706899
Fax
400-8706899
Email
hysj_bj.com
Country
China
ProdList
3585
Advantage
55
Bide Pharmatech Ltd.
Tel
400-1647117 15221909166
Fax
+86-21-61629029
Email
product02@bidepharm.com
Country
China
ProdList
41438
Advantage
60
RiZhao LiDeShi Chemical Co., Ltd.
Tel
010-51268198
Fax
010-63833209
Email
leadershipchem@126.com
Country
China
ProdList
2549
Advantage
58
Mei Lan Industrial (Shanghai) Co., Ltd.
Tel
021-58958189
Fax
021-58957967
Email
wouchina@126.com
Country
China
ProdList
2671
Advantage
55
ChemStrong Scientific Co.,Ltd
Tel
0755-0755-66853366 13670046396
Fax
0755-28363542
Email
sales@chem-strong.com
Country
China
ProdList
17982
Advantage
56
Shanghai ideal Industrial Co., Ltd.
Tel
021-58957966 18930537195
Fax
021-60899437
Email
wouchina@126.com
Country
China
ProdList
3033
Advantage
58
Chengdu HuaXia Chemical Reagent Co. Ltd
Tel
400-1166-196 13458535857
Fax
QQ:800101999
Email
cdhxsj@163.com
Country
China
ProdList
13358
Advantage
58
Wuxi Zhongkun Biochemical Technology Co., Ltd.
Tel
0510-85629785 18013409632
Fax
051085625359
Email
sales@reading-chemicals.com
Country
China
ProdList
15185
Advantage
58
More
Less

View Lastest Price from Acetamide manufacturers

Hebei Zhuanglai Chemical Trading Co.,Ltd
Product
Acetamide 60-35-5
Price
US $100.00/kg
Min. Order
1kg
Purity
99
Supply Ability
5000
Release date
2024-04-24
Shaanxi Dideu Medichem Co. Ltd
Product
Acetamide 60-35-5
Price
US $1.10/g
Min. Order
1g
Purity
99.0% min
Supply Ability
100 tons min
Release date
2021-05-25
Wuhan Boyuan Import & Export Co., LTD
Product
Acetamide 60-35-5
Price
US $1.00/g
Min. Order
1g
Purity
99.99%
Supply Ability
500tons
Release date
2024-04-07

60-35-5, AcetamideRelated Search:


  • ACETAMIDE
  • ACETIC ACID AMIDE
  • Acetamidum
  • AMIDE C2
  • Acetamid
  • Acetamid(trigonaleForm)
  • acetamide(ethanamide)
  • aceticacidamide[qr]
  • acetimidicacid
  • acetimidicacid[qr]
  • nci-c02108[qr]
  • LABOTEST-BB LT00795814
  • ETHANAMIDE
  • Amide C<SUB>2</SUB>
  • AMMONIOM-ACETATE
  • Acetamide,Amide C2
  • Acetamide, extra pure
  • Acetamide, Zone Refined (number of passes:37)
  • AcetaMide, pure, 99% 100GR
  • AcetaMide, pure, 99% 500GR
  • Acetamide;Acetic acid;Acetic acid amine;Ethanamide
  • Acetic acid amine
  • ACETAMIDE, 98+%
  • ACETAMIDE, PCR REAGENT
  • ACETAMIDE, SUBLIMED, ZONE-REFINED, 99%
  • ACETAMIDE GR 99%
  • ACETAMIDE HPLC 99+%
  • ACETAMIDEGC STANDARD
  • ACETAMIDE MOLECULAR BIOLOGY REAGENT
  • AcetamideForSynthesis
  • Acetamide,99%
  • Acetamide, extra pure, 99+%
  • Acetamide, pure, 99%
  • ACETAMIDE REAGENT
  • ACETAMIDE,CRYSTAL,REAGENT
  • Actamide
  • ACETAMIDE extrapure AR
  • Acetamide, 99%, pure
  • 1-Hydroxyethanimine
  • 1-Iminoethanol
  • Acetamide,99+%,extra pure
  • Acetamide/Ethyl cyanoacetate
  • Acetylamide
  • acetylamine
  • Amid kyseliny octove
  • amidkyselinyoctove
  • CH3CONH2
  • Essigsαureamid
  • ethanamide[qr]
  • Methanecarboxamide
  • methanecarboxamide[qr]
  • NCI-C02108
  • AcetaMide 0.25
  • Acetamide sublimed, 99%
  • ACETAMIDE >= 99.0% (GC)
  • Acetamide≥ 99% (Assay)
  • Apremilast impurity HS093202
  • Daclatasvir Impurity-S