ChemicalBook > CAS DataBase List > OCHRATOXIN B

OCHRATOXIN B

Product Name
OCHRATOXIN B
CAS No.
4825-86-9
Chemical Name
OCHRATOXIN B
Synonyms
OCHRATOXIN B;(r)-carbonyl);Ochratoxin B(OTB);ochratoxin b solution;Ochratoxin B in Methanol;Ochratoxin B 10ug/ml in ACN;Ochratoxin B in acetonitrile;Ochratoxin B 10.0 μg/ml Acetonitrile;ochratoxin B from aspergillus ochraceus;U-[13C20]- Ochratoxin B in Acetonitrile
CBNumber
CB2297543
Molecular Formula
C20H19NO6
Formula Weight
369.37
MOL File
4825-86-9.mol
More
Less

OCHRATOXIN B Property

Melting point:
221° (van der Merwe)
alpha 
D -35° (c = 0.15 in ethanol)
Boiling point:
632.4±55.0 °C(Predicted)
Density 
1.361±0.06 g/cm3(Predicted)
Flash point:
-11 °C
storage temp. 
2-8°C
solubility 
DMF: 10 mg/ml; DMSO: 15 mg/ml; Ethanol: 50 mg/ml; Ethanol:PBS (pH 7.2) (1:1): 0.50 mg/ml
form 
A crystalline solid
pka
3.40±0.10(Predicted)
color 
White to off-white
EPA Substance Registry System
L-Phenylalanine, N-[[(3R)-3,4-dihydro-8-hydroxy-3-methyl-1-oxo-1H-2-benzopyran-7-yl]carbonyl]- (4825-86-9)
More
Less

Safety

Hazard Codes 
Xn,T,F
Risk Statements 
22-36/37/38-65-48/23/24/25-36/38-11-46-45-36-20/21/22
Safety Statements 
26-36-45-16-53-36/37-62
RIDADR 
UN 3462 6.1/PG 3
WGK Germany 
3
RTECS 
AY6825000
HazardClass 
6.1(a)
PackingGroup 
I
HS Code 
39229000
Hazardous Substances Data
4825-86-9(Hazardous Substances Data)
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H225Highly Flammable liquid and vapour

H302Harmful if swallowed

H312Harmful in contact with skin

H319Causes serious eye irritation

H332Harmful if inhaled

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

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

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
32411
Product name
Ochratoxin B solution
Purity
10?μg/mL in acetonitrile, analytical standard
Packaging
1ML
Price
$531
Updated
2025/07/31
Cayman Chemical
Product number
16167
Product name
Ochratoxin B
Purity
≥98%
Packaging
500μg
Price
$111
Updated
2024/03/01
Cayman Chemical
Product number
16167
Product name
Ochratoxin B
Purity
≥98%
Packaging
1mg
Price
$210
Updated
2024/03/01
Cayman Chemical
Product number
16167
Product name
Ochratoxin B
Purity
≥98%
Packaging
5mg
Price
$601
Updated
2024/03/01
Usbiological
Product number
O5305-04
Product name
Ochratoxin B
Packaging
1mg
Price
$426
Updated
2021/12/16
More
Less

OCHRATOXIN B Chemical Properties,Usage,Production

Description

Ochratoxins are mycotoxins produced by Aspergillus and Penicillium species of fungi that contaminate foods. Ochratoxin A (OTA, ) is a chlorinated form with toxicity that targets the kidneys, causing nephropathy and renal adenomas. OTB is a non-chlorinated analog of OTA that has cytotoxic effects on kidney and liver cells in vitro but only minor effects in vivo, due to its rapid metabolism and excretion. OTB inhibits cell proliferation of human liver HepG2 cells at doses as low as 1 μg/ml but lacks the genotoxic activity of OTA, even at higher concentrations.

Uses

Ochratoxins are toxic metabolites from Aspergillus orchraceus.

Uses

Ochratoxin B is the non-chlorinated analogue of the much more extensively studied ochratoxin A. It is co-produced by the same species of Aspergillus and Penicillium that are associated with food spoilage. Ochratoxin B has received little focused investigation and its mode of action and potential hazards have been inferred from ochratoxin A.

Definition

ChEBI: Ochratoxin B is a phenylalanine derivative resulting from the formal condensation of the amino group of L-phenylalanine with the carboxy group of (3R)-8-hydroxy-3-methyl-1-oxo-3,4-dihydro-1H-2-benzopyran-7-carboxylic acid. Ochratoxin B differs from the more naturally abundant ochratoxin A in the absence of the dihydroisocoumarin chlorine atom. It has cytotoxic effects on kidney and liver cells in vitro but only minor effects in vivo, due to its rapid metabolism and excretion. It inhibits cell proliferation of human liver HepG2 cells at doses as low as 1 mug/ ml but lacks the genotoxic activity of ochratoxin A, even at higher concentrations. It has a role as an Aspergillus metabolite, a Penicillium metabolite, a mycotoxin and a calcium channel blocker. It is a phenylalanine derivative, a N-acyl-L-phenylalanine, a member of isochromanes and a monocarboxylic acid. It is a conjugate acid of an ochratoxin B(1-).

General Description

Crystals that exhibit blue fluorescence.

Reactivity Profile

OCHRATOXIN B is incompatible with strong oxidizing agents, strong acids and strong bases. OCHRATOXIN B is a carboxylic acid derivative. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt.

Fire Hazard

Flash point data for OCHRATOXIN B are not available. OCHRATOXIN B is probably combustible.

References

[1] J VARGA. Ochratoxin production by Aspergillus species.[J]. Applied and Environmental Microbiology, 1996, 62 12: 4461-4464. DOI: 10.1128/aem.62.12.4461-4464.1996
[2] SIEGFRIED KNASMüLLER. Structurally related mycotoxins ochratoxin A, ochratoxin B, and citrinin differ in their genotoxic activities and in their mode of action in human-derived liver (HepG2) cells: implications for risk assessment.[J]. Nutrition and Cancer-An International Journal, 2004, 50 2: 190-197. DOI: 10.1207/s15327914nc5002_9
[3] E. O’BRIEN  Daniel R D  A Prietz. Investigation of the teratogenic potential of ochratoxin A and B using the FETAX system[J]. Birth defects research. Part B, Developmental and reproductive toxicology, 2005, 74 5: 417-423. DOI: 10.1002/bdrb.20054
[4] C N EZEKIEL. Fungal and bacterial metabolites in commercial poultry feed from Nigeria.[J]. Food Additives and Contaminants Part A-chemistry Analysis Control Exposure & Risk Assessment, 2012, 29 8: 1288-1299. DOI: 10.1080/19440049.2012.688878

OCHRATOXIN B Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

OCHRATOXIN B Suppliers

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
32321
Advantage
50
Guangzhou Isun Pharmaceutical Co., Ltd
Tel
020-39119399 18927568969
Fax
020-39119999
Email
isunpharm@qq.com
Country
China
ProdList
4720
Advantage
55
Shanghai Macklin Biochemical Co.,Ltd.
Tel
15221275939
Fax
021-50706099
Email
shenlinxing@macklin.cn
Country
China
ProdList
15873
Advantage
55
Alta Scientific Co., Ltd.
Tel
022-6537-8550 15522853686
Fax
022-2532-9655
Email
sales@altasci.com.cn
Country
China
ProdList
4511
Advantage
55
Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Fax
021-65675885
Email
info@efebio.com
Country
China
ProdList
9803
Advantage
58
Shanghai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847; 18021002903
Fax
QQ:3008007432
Email
3008007409@qq.com
Country
China
ProdList
71826
Advantage
60
Qingdao IniKem BioPharmaTech Co.,Ltd
Tel
0532-58268780 18561687109;
Fax
-
Email
sales@inikem.com
Country
China
ProdList
298
Advantage
55
ShangHai Biochempartner Co.,Ltd
Tel
177-54423994 17754423994
Fax
QQ:2853530913
Email
2853530910@QQ.com
Country
China
ProdList
8000
Advantage
62
Shanghai SuperLan Chemcial Technique Centre
Tel
0-2022843681 15618226720
Fax
+86-21-51601218
Email
chaolaichem@foxmail.com
Country
China
ProdList
12475
Advantage
58
Lynnchem
Tel
86-(0)29-85992781 17792393971
Email
info@lynnchem.com
Country
China
ProdList
4587
Advantage
58
Shanghai Hongye Biotechnology Co. Ltd
Tel
400-9205774
Email
sales@glpbio.cn
Country
China
ProdList
6777
Advantage
58
Shenzhen Polymeri Biochemical Technology Co., Ltd.
Tel
+86-400-002-6226 +86-13028896684;
Email
sales@rrkchem.com
Country
China
ProdList
57422
Advantage
58
ChemeGen(Shanghai) Biotechnology Co.,Ltd.
Tel
18818260767
Fax
QQ 3610331285
Email
sales@chemegen.com
Country
China
ProdList
11218
Advantage
58
Shaanxi Dideu Medichem Co. Ltd
Tel
+86-29-81139210 +86-18192627656
Fax
+86-29-88380327
Email
1059@dideu.com
Country
China
ProdList
3588
Advantage
58
ShangHai Anpel Co, Ltd.
Tel
18501792038 18502138905
Email
shanpel@anpel.com.cn
Country
China
ProdList
9611
Advantage
58
Meng Cheng Technology (Shanghai) Co., LTD
Tel
400-820-6829
Email
sales@mitachieve.com
Country
China
ProdList
8860
Advantage
58
Shanghai Hewu Biotechnology Co., LTD
Tel
021-57886085 17317861055
Email
shhebio@126.com
Country
CHINA
ProdList
7974
Advantage
58
Wuhan Dingxintong Pharmaceutical Co. , Ltd.
Tel
15871722230
Fax
2796190295
Email
15871722230@163.com
Country
China
ProdList
4686
Advantage
58
Nanjing Shizhou Biology Technology Co.,Ltd
Tel
025-85560043 13675144456
Fax
025-85563444
Email
sean.lv@synzest.com
Country
China
ProdList
11438
Advantage
58
Wuhan Yanzhe Technology Co., Ltd
Tel
15527250409
Fax
QQ:2692360204
Email
wenhaotian12@163.com
Country
China
ProdList
4171
Advantage
58
Energy Chemical
Tel
021-58432009 400-005-6266
Fax
021-58436166
Email
marketing@energy-chemical.com
Country
China
ProdList
44918
Advantage
58
cjbscvictory
Tel
13348960310
Email
3003867561@qq.com
Country
China
ProdList
10503
Advantage
58
Hubei yongkuo Technology Co., Ltd
Tel
027-027-59223108 15972152991
Fax
027-59223108
Email
1248580099@qq.com
Country
China
ProdList
9953
Advantage
58
Hubei Wande Chemical Co., Ltd
Tel
027-027-59210159 15377098680
Fax
027-59210159
Email
1148280011@qq.com
Country
China
ProdList
9835
Advantage
58
TCI (Shanghai) Chemical Trading Co., Ltd.
Tel
021-61109150
Fax
021-61105897
Email
sales@tcisct.com
Country
China
ProdList
29668
Advantage
58
Beijing Jin Ming Biotechnology Co., Ltd.
Tel
010-60605840 15801484223;
Email
psaitong@jm-bio.com
Country
China
ProdList
29757
Advantage
58
Guangdong wengjiang Chemical Reagent Co., Ltd.
Tel
0751-2815987 13927875076
Fax
0751-2828607
Email
3007432263@qq.com
Country
China
ProdList
9963
Advantage
58
Shanghai Moqi Biological Technology Co., LTD
Tel
021-38218169 13681877033
Email
2702713455@qq.com
Country
China
ProdList
9997
Advantage
58
TargetMol Chemicals Inc.
Tel
4008200310
Email
marketing@tsbiochem.com
Country
China
ProdList
24961
Advantage
58
Naturewill Biotechnology Co., Ltd.
Tel
028-82632533 18113192475
Email
3157321941@qq.com
Country
China
ProdList
4993
Advantage
58
Qiyuan (Guangdong) Pharmaceutical Chemical Co., Ltd.
Tel
18026564465
Email
304903156@qq.com
Country
China
ProdList
8000
Advantage
58
Shanghai Saikerui Biotechnology Co. , Ltd.
Tel
021-58000709 15900491054
Email
info@scrbio.com
Country
China
ProdList
9881
Advantage
58
Shaanxi Xihua Chemical Industry Co., Ltd
Tel
029-029-81123119 17391733320
Email
1021@dideu.com
Country
China
ProdList
9995
Advantage
58
Nanjing Shizhou Biology Technology Co.,Ltd
Tel
025-85560043 15850508050
Fax
025-85563444
Email
cindy.huang@synzest.com
Country
China
ProdList
12000
Advantage
58
Shanghai Aladdin Biochemical Technology Co.,Ltd.
Tel
400-6206333 13167063860
Email
anhua.mao@aladdin-e.com
Country
China
ProdList
48457
Advantage
58
Tanmo Quality Inspection Technology Co., Ltd.
Tel
4008-099-669
Email
23419001name@qq.com
Country
CHINA
ProdList
6043
Advantage
58
BePure (Beijing) Biotechnology Co.
Tel
58896805
Email
7993601name@qq.com
Country
CHINA
ProdList
6620
Advantage
58
Beijing Putian Tongchuang Biotechnology Co., Ltd.
Tel
18201332838
Email
3032079623@qq.com
Country
China
ProdList
6695
Advantage
58
Shanghai Weiyite Biotechnology Co., Ltd
Tel
15317051735
Email
zhaojing@wytsci.com
Country
China
ProdList
9980
Advantage
58
Sangon Biotech (Shanghai) Co.,Ltd.
Tel
400-821-026
Email
Sales@sangon.com
Country
China
ProdList
6710
Advantage
58
Chengdu DeSiTe Biological Technology Co., Ltd
Tel
17308096051
Email
3001048290@qq.com
Country
China
ProdList
6219
Advantage
58
Cayman Chemical Company
Tel
800-364-9897
Email
sales@caymanchem.com
Country
China
ProdList
6838
Advantage
58
Enzo Biochem Inc
Tel
Enzo Biochem Inc. 13797054060
Email
Enzoname@qq.com
Country
China
ProdList
6174
Advantage
58
Merck KGaA
Tel
21-20338288
Email
ordercn@merckgroup.com
Country
China
ProdList
6394
Advantage
58
Santa Cruz Biotechnology Inc
Tel
021-60936350
Email
scbt@scbt.com
Country
China
ProdList
6594
Advantage
58
ATK CHEMICAL COMPANY LIMITED
Tel
+undefined-21-51877795
Fax
+86 21 5161 9052/ 5187 7796
Email
ivan@atkchemical.com
Country
China
ProdList
33024
Advantage
60
DAYANG CHEM (HANGZHOU) CO.,LTD
Tel
+86-88938639 +86-17705817739
Email
info@dycnchem.com
Country
China
ProdList
53899
Advantage
58
Shaanxi Cuikang Pharmaceutical Technology Co., Ltd
Tel
+8618791163155
Email
18791163155@163.com
Country
China
ProdList
3397
Advantage
58
ShenZhen Trendseen Biological Technology Co.,Ltd.
Tel
13417589054
Email
trendseenbio@gmail.com
Country
China
ProdList
11681
Advantage
58
More
Less

View Lastest Price from OCHRATOXIN B manufacturers

Shaanxi Dideu Medichem Co. Ltd
Product
Ochratoxin B 4825-86-9
Price
US $1.00-22.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
100000KG
Release date
2024-07-29

4825-86-9, OCHRATOXIN BRelated Search:


  • 2-[((3R)-8-HYDROXY-3-METHYL-1-OXOISOCHROMAN-7-YL)CARBONYLAMINO](2S)-3-PHENYLPR OPANOIC ACID
  • Ochratoxin B(OTB)
  • Ochratoxin B, 99%, from Aspergillus ochraceus
  • OCHRATOXIN B
  • (r)-carbonyl)
  • l-phenylalanine,n-((3,4-dihydro-8-hydroxy-3-methyl-1-oxo-1h-2-benzopyran-7-yl)
  • N-[(8-Hydroxy-3-Methyl-1-oxo-7-isochroManyl)carbonyl]-3-phenyl-L- alanine
  • N-[[(3R)-3,4-Dihydro-8-hydroxy-3-Methyl-1-oxo-1H-2-benzopyran-7-yl]carbonyl]-L-phenylalanine
  • ochratoxin B from aspergillus ochraceus
  • ochratoxin b from aspergillus ochraceus (aspergillus oryzae)
  • ochratoxin b solution
  • (-)-N-[[(R)-3,4-Dihydro-8-hydroxy-3-methyl-1-oxo-1H-2-benzopyran-7-yl]carbonyl]-L-phenylalanine
  • N-[[(3R)-1-Oxo-3-methyl-8-hydroxy-3,4-dihydro-1H-2-benzopyran-7-yl]carbonyl]-L-phenylalanine
  • N-[[(R)-1-Oxo-3α-methyl-8-hydroxyisochroman-7-yl]carbonyl]-L-phenylalanine
  • (2S)-2-[[(3R)-8-hydroxy-1-keto-3-methyl-isochromane-7-carbonyl]amino]-3-phenyl-propionic acid
  • (2S)-2-[[(3R)-8-hydroxy-3-methyl-1-oxo-3,4-dihydroisochromen-7-yl]carbonylamino]-3-phenyl-propanoic acid
  • (2S)-2-[[(3R)-8-hydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-7-carbonyl]amino]-3-phenylpropanoic acid
  • Ochratoxin B Solution (10μg/ml in Acetonitrile Solution)
  • L-Phenylalanine, N-[[(3R)-3,4-dihydro-8-hydroxy-3-methyl-1-oxo-1H-2-benzopyran-7-yl]carbonyl]-
  • Ochratoxin B 10ug/ml in ACN
  • (2S)-2-[[(3R)-8-hydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-7-carbonyl]amino]-3-phenylpropanoicaci
  • Ochratoxin B in acetonitrile
  • Ochratoxin B in Methanol
  • U-[13C20]- Ochratoxin B in Acetonitrile
  • Ochratoxin B 10.0 μg/ml Acetonitrile
  • Ochratoxin A and B Mixture 592 10 μg/mL in Acetonitrile
  • 4825-86-9
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Metabolites & Impurities
  • Pharmaceuticals
  • Cell Signaling and Neuroscience
  • Mold
  • Toxins and Venoms
  • Biotoxins
  • Mycotoxins
  • Single component solutions