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ACETYLENEDICARBOXAMIDE

Product Name
ACETYLENEDICARBOXAMIDE
CAS No.
543-21-5
Chemical Name
ACETYLENEDICARBOXAMIDE
Synonyms
Renamycin;Lenamycin;Aquamycin;4-Dioxane-2;2-BUTYNEDIAMIDE;but-2-ynediaMide;ACETYLENEDICARBOXAMIDE;1,2-Ethynedicarboxamide;Acetylendicarbonsaeureamid;acetylenedicarboxylicaciddiamide
CBNumber
CB7103786
Molecular Formula
C4H4N2O2
Formula Weight
112.09
MOL File
543-21-5.mol
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ACETYLENEDICARBOXAMIDE Property

Melting point:
179 °C
Boiling point:
209.98°C (rough estimate)
Density 
1.4421 (rough estimate)
refractive index 
1.4610 (estimate)
storage temp. 
Store at -20°C
solubility 
DMF: 10 mg/ml; DMSO: 20 mg/ml; DMSO:PBS (pH 7.2) (1:7): 0.12 mg/ml
form 
Fine Crystalline Powder
pka
13.01±0.50(Predicted)
color 
Cream to beige
EPA Substance Registry System
2-Butynediamide (543-21-5)
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Safety

Hazard Codes 
T
Risk Statements 
25-21
Safety Statements 
45-36/37-28A
HS Code 
29241900
Toxicity
LD50 i.v. in mice: 11 mg/kg (Suzuki)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P330Rinse mouth.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Cayman Chemical
Product number
23637
Product name
Cellocidin
Purity
≥95%
Packaging
5mg
Price
$97
Updated
2024/03/01
Cayman Chemical
Product number
23637
Product name
Cellocidin
Purity
≥95%
Packaging
10mg
Price
$156
Updated
2024/03/01
Cayman Chemical
Product number
23637
Product name
Cellocidin
Purity
≥95%
Packaging
25mg
Price
$340
Updated
2024/03/01
Cayman Chemical
Product number
23637
Product name
Cellocidin
Purity
≥95%
Packaging
50mg
Price
$631
Updated
2024/03/01
TRC
Product number
C255953
Product name
Cellocidin
Packaging
5mg
Price
$305
Updated
2021/12/16
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ACETYLENEDICARBOXAMIDE Chemical Properties,Usage,Production

Description

Cellocidin is an antibiotic originally isolated from S. chibaensis. It is active against various bacterial strains including M. tuberculosis and against the trypanosomes T. brucei and T. rhodesiense (IC50s = 150 and 30 ng/ml, respectively). It inhibits proliferation of LCL1 and LCL2 cells transformed by Epstein-Barr virus (EBV), activates the c-Myc and NF-κB pathways in BC3 and LCL1 cells, and induces necrotic cell death in B cells infected with gammaherpes virus. Cellocidin (100-200 ppm) is protective against bacterial leaf blight in rice plants and inhibits α-ketoglutarate oxidation in X. oryzae, the bacterium that causes leaf blight, when used at a concentration of 1 ppm, suggesting that it inhibits the citric acid cycle. Formulations containing cellocidin have been used as agricultural pesticides.

Chemical Properties

CREAM TO BEIGE FINE CRYSTALLINE POWDER

Uses

Cellocidin is a small neutral alkyne produced by a number of Streptomyces species, first discovered by Suzuki and colleagues in 1958. Cellocidin has a broad antibacterial, antifungal and antitumor profile due to its ability to react with endogenous thiols like cysteine and glutathione. Cellocidin occurs as a weak active in many bioassays using actinomycete crude extracts and is thus a useful standard for chemical and bioassay dereplication.

Definition

ChEBI: A dicarboxylic acid diamide resulting from the formal condensation of both of the carboxy groups of butynedioic acid with ammonia. An antibacterial agent produced by Streptomyces chibaensis.

Purification Methods

Acetylenedicarboxamide crystallises from MeOH and H2O [m 190-192o(dec) as hemihydrate]. When prepared from the ester + NH3 it has m 213o(dec). Also a melting point of 290-292o(dec) has been reported. [Saggimo J Org Chem 22 1171 1857, Kharash et al. J Org Chem 10 392 1945, Blomquist & Winslow J Org Chem 10 156 1945, Beilstein 2 I 317, 2 III 1995, 2 IV 2295.]

ACETYLENEDICARBOXAMIDE Preparation Products And Raw materials

Raw materials

Preparation Products

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ACETYLENEDICARBOXAMIDE Suppliers

Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Fax
86-21-50328109
Email
3bsc@sina.com
Country
China
ProdList
15839
Advantage
69
Hangzhou Yuhao Chemical Technology Co., Ltd
Tel
0571-82693216
Fax
+86-571-82880190
Email
info@yuhaochemical.com
Country
China
ProdList
9387
Advantage
52
Hangzhou Sage Chemical Co., Ltd.
Tel
+86057186818502 13588463833
Fax
Pls mail us for more information!
Email
info@sagechem.com
Country
China
ProdList
10266
Advantage
58
Thermo Fisher Scientific
Tel
800-810-5118
Fax
+86-10-84193589
Email
cnchemical@thermofisher.com
Country
China
ProdList
17770
Advantage
75
Shanghai XinKai Chemical Technology Co., Ltd.
Tel
021-58930698 15921516558
Fax
86-021-58933679
Email
zhangyichao84@126.com
Country
China
ProdList
916
Advantage
55
Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Fax
021-65675885
Email
info@efebio.com
Country
China
ProdList
9806
Advantage
58
Lynnchem
Tel
86-(0)29-85992781 17792393971
Email
info@lynnchem.com
Country
China
ProdList
4587
Advantage
58
Novachemistry
Tel
44-20819178-90 02081917890
Fax
(0)2080432064
Email
info@novachemistry.com
Country
United Kingdom
ProdList
4381
Advantage
58
Aikon International Limited
Tel
025-58851090 13611564524
Fax
(6)02557626880
Email
lwan@aikonchem.com
Country
China
ProdList
15951
Advantage
58

543-21-5, ACETYLENEDICARBOXAMIDERelated Search:


  • Acetylendicarbonsaeureamid
  • Acetylenedicarboxylic acid diamide
  • acetylenedicarboxylicaciddiamide
  • Aquamycin
  • Lenamycin
  • Renamycin
  • 2-BUTYNEDIAMIDE
  • ACETYLENEDICARBOXAMIDE
  • ACETYLENEDICARBOXAMIDE (PRACT), 95%
  • 1,2-Ethynedicarboxamide
  • Acetylenedicarboxamide,95%,pract.
  • Acetylenedicarboxamide2-Butynediamide
  • but-2-ynediaMide
  • AquaMycin, ButynesiaMide, LenaMycin
  • 4-Dioxane-2
  • 543-21-5