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PENICILLIC ACID

Product Name
PENICILLIC ACID
CAS No.
90-65-3
Chemical Name
PENICILLIC ACID
Synonyms
NSC 402844;pencillicacid;PENICILLINACID;PENICILLIC ACID;kyselinapenicilova;PENICILLIC ACID 99%;Penicillic acid,99%;Penicillic acid, 99% 25MG;Benzylpenicillin Impurity 26;3-methoxy-5-methyl-4-oxo-5-hexadienoicacid
CBNumber
CB0338325
Molecular Formula
C8H10O4
Formula Weight
170.16
MOL File
90-65-3.mol
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PENICILLIC ACID Property

Melting point:
83-87 °C
Boiling point:
219.79°C (rough estimate)
Density 
1.1456 (rough estimate)
refractive index 
1.4425 (estimate)
storage temp. 
Store at 2-8
solubility 
DMSO: >10mg/mL
pka
3.90±0.33(Predicted)
form 
solid
color 
Needles from pet ether or rhombic orhexagonal plates
Merck 
13,7163
CAS DataBase Reference
90-65-3
IARC
3 (Vol. 10, Sup 7) 1987
EPA Substance Registry System
Penicillic acid (90-65-3)
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Safety

Hazard Codes 
Xn,T
Risk Statements 
36/37/38-20/21/22-22
Safety Statements 
37/39-26-24/25
RIDADR 
2811
RTECS 
MM2625000
HazardClass 
6.1(b)
PackingGroup 
III
HS Code 
29189900
Hazardous Substances Data
90-65-3(Hazardous Substances Data)
Toxicity
LD50 i.p. in mice: 90.00 mg/kg (Chan et al.)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P260Do not breathe dust/fume/gas/mist/vapours/spray.

P271Use only outdoors or in a well-ventilated area.

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N-Bromosuccinimide Price

Cayman Chemical
Product number
11440
Product name
Penicillic Acid
Purity
≥98%
Packaging
5mg
Price
$49
Updated
2024/03/01
Cayman Chemical
Product number
11440
Product name
Penicillic Acid
Purity
≥98%
Packaging
10mg
Price
$92
Updated
2024/03/01
Cayman Chemical
Product number
11440
Product name
Penicillic Acid
Purity
≥98%
Packaging
25mg
Price
$216
Updated
2024/03/01
TRC
Product number
P223530
Product name
PenicillicAcid
Packaging
50mg
Price
$1760
Updated
2021/12/16
ChemScene
Product number
CS-0034504
Product name
Penicillicacid
Purity
>99.0%
Packaging
5mg
Price
$50
Updated
2021/12/16
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PENICILLIC ACID Chemical Properties,Usage,Production

Description

Gram negative bacteria utilize N-acylated homoserine lactones to coordinate expression of virulence in response to the density of the surrounding bacterial population in a process termed quorum sensing. By interfering with this communication and thereby disrupting virulence expression, quorum sensing inhibitors are emerging as an alternative to the conventional ways of fighting bacterial infections. Penicillic acid is a mycotoxin produced from Penicillium species identified in molds on corn and other grains. At 80 μM, penicillic acid inhibits bacterial quorum sensing communication in P. aeruginosa by selectively repressing various virulence factor and other quorum sensing-regulated genes. It has been shown to inhibit Fas-mediated apoptosis at 100-200 μM by targeting caspase-8 activity in Burkitt’s lymphoma Raji cells.

Chemical Properties

white to light beige crystals or powder

Uses

Gram negative bacteria utilize N-acylated homoserine lactones to coordinate expression of virulence in response to the density of the surrounding bacterial population in a process termed quorum sensing. By interfering with this communication and thereby disrupting virulence expression, quorum sensing inhibitors are emerging as an alternative to the conventional ways of fighting bacterial infections. Penicillic acid is a mycotoxin produced from Penicillium species identified in molds on corn and other grains. At 80 μM, penicillic acid inhibits bacterial quorum sensing communication in P. aeruginosa by selectively repressing various virulence factor and other quorum sensing-regulated genes. It has been shown to inhibit Fas-mediated apoptosis at 100-200 μM by targeting caspase-8 activity in Burkitt’s lymphoma Raji cells.

Uses

Penicillic acid can be isolated from the seed-borne fungus Aspergillus persii EML-HPB1-11 and it exhibits antibacterial activity against various plant pathogenic bacteria. This compound can be a potential lead molecule for developing synthetic agrochemicals. Penicillic acid is also used as a quorum sensing inhibitor.

Safety Profile

Poison by intravenous, subcutaneous, and intraperitoneal routes. Moderately toxic by ingestion. An experimental teratogen. Experimental reproductive effects. Questionable carcinogen with experimental neoplastigenic data. Human mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes.

in vitro

the compound was active primarily against gram-negative bacteria, and it was also active against some gram-positive species. it showed limited antihelminthic properties but did affect the growth of oat seed coleoptiles by interference with the respiratory process. penicillic acid has proven to be too toxic for use in therapy [1]. penicillic acid (80 μm) inhibited bacterial quorum sensing communication in p. aeruginosa by selectively repressing various virulence factor and other quorum sensing-regulated genes [2]. in burkitt’s lymphoma raji cells, penicillic acid exihibited an inhibitory effect on fas-mediated apoptosis at 100-200 μm by targeting caspase-8 activity [3].

in vivo

the ldso (subcutaneous injection) for mice is 100 mg/kg. subcutaneous injection of 1.0 mg/dose twice weekly produced transplantable tumors after 64 weeks in all rats surviving treatment. in addition, a dose at 0.1 mg initiated tumor development [1].

Purification Methods

The lactone (furanone, anhydrous) hydrolyses to the acid (3-methoxy-4-oxo-hexa-2,5-dienoic acid, hydrate). It crystallises from water as the monohydrate (acid), or from pet ether as the anhydrous (lactone) compound. The free acid is in equilibrium with the lactone. UV: max 221nm ( 12,500) in 0.02M KOH; 228nm ( 11,500) in 0.02M HCl [Raphael J Chem Soc 1508 1948]. [Beilstein 3 II 519, 3 III 1467.] It is a possible antineoplastic.

References

[1] ciegler a, detroy r w, lillehoj e b. patulin, penicillic acid, and other carcinogenic lactones[j]. microbial toxins, 1971, 6: 409-434.
[2] rasmussen t b, skindersoe m e, bjarnsholt t, et al. identity and effects of quorum-sensing inhibitors produced by penicillium species[j]. microbiology, 2005, 151(5): 1325-1340.
[3] bando m, hasegawa m, tsuboi y, et al. the mycotoxin penicillic acid inhibits fas ligand-induced apoptosis by blocking self-processing of caspase-8 in death-inducing signaling complex[j]. journal of biological chemistry, 2003, 278(8): 5786-5793.

PENICILLIC ACID Preparation Products And Raw materials

Raw materials

Preparation Products

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PENICILLIC ACID Suppliers

J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
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86-10-82849933
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jkinfo@jkchemical.com
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China
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Meryer (Shanghai) Chemical Technology Co., Ltd.
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4006608290; 18621169109
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86-21-61259102
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market03@meryer.com
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China
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BOC Sciences
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1-631-485-4226; 16314854226
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info@bocsci.com
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United States
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Beijing HuaMeiHuLiBiological Chemical
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010-56205725
Fax
010-65763397
Email
waley188@sohu.com
Country
China
ProdList
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Beijing innoChem Science & Technology Co.,Ltd.
Tel
400-810-7969 010-59572699
Fax
010-59572688
Email
ningzi.li@inno-chem.com.cn
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China
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ChemStrong Scientific Co.,Ltd
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0755-66853366 13670046396
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0755-28363542
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sales@chem-strong.com
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China
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Shanghai EFE Biological Technology Co., Ltd.
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021-65675885 18964387627
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021-65675885
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China
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Shanghai YuanYe Biotechnology Co., Ltd.
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021-61312847; 18021002903
Fax
QQ:3008007432
Email
3008007409@qq.com
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China
ProdList
27322
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Shandong Xiya Chemical Co., Ltd.
Tel
4009903999 13395398332
Fax
0539-6365991
Email
sales@xiyashiji.com
Country
China
ProdList
20810
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Beijing Jin Ming Biotechnology Co., Ltd.
Tel
010-60605840 18892239720
Fax
010-60605840
Email
psaitong@jm-bio.com
Country
China
ProdList
12308
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View Lastest Price from PENICILLIC ACID manufacturers

Henan Fengda Chemical Co., Ltd
Product
PENICILLIC ACID 90-65-3
Price
US $8.00-1.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
g-kg-tons, free sample is available
Release date
2024-04-03

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