Food safety is an important concern that includes handling, preparation and storage of food ingredients in ways that prevent poisoning. Unhealthy food creates a cycle of disease and malnutrition that affects infants and adults as well. Foods can be contaminated by microorganisms such as bacteria, viruses, parasites or fungi. There are specific bacteria which are the primary causes of foodborne diseases; among them: Escherichia coli, Salmonella enterica, Campylobacter jejuni, Staphylococcus aureus, Listeria monocytogenes, and Bacillus cereus. These microbes might have been present before the food was harvested or collected, or they could have been introduced during handling or preparation. Pesticides and veterinary drugs introduced to protect plants and animals from pests and diseases could later unintentionally result in contamination of the food products derived from these sources (e.g. mycotoxins, heavy metals or persistent organic pollutants).

The necessity to determine pathogenic organisms and their toxins serves as a fundamental requirement to guarantee the safety and quality of our food supplies. Detection methods with enhanced sensitivity and rapid results are a prerequisite to achieve efficient tests.

Fermentek supports customers globally with a wide range of food-safety related products to ensure the integrity of customers’ needs. Our food safety testing materials can be used for determination of contaminants or toxins. Also, our test procedure can determine and quantify adulterants, hazardous chemicals or pathogens present in food that can have a dangerous influence on human health.

Food Safety Related Products

Food-safety related products produced by Fermentek include natural toxins which may occur in foodstuffs and standard "ready to use" solutions (Mycotoxin Standards) of toxins containing known accurate amounts in commonly used solvents. The standard solutions serve as quantitatively reliable samples of the toxic materials, which can be compared to tested samples of food by conventional analytical methods.

Mycotoxin Food Safety Standards

Fermentek is a global leader in the production of certified Mycotoxin reference materials for food safety labs and for R&D use. Mycotoxins are toxic fungal metabolites that may appear in food and feed as a result of fungal infection of crops such as cereals, dried fruit and many other agricultural products.

Accurate analysis of Mycotoxins depends upon the use of certified Mycotoxin standard reference materials used for calibration and validation of food safety analytical instruments and methods. High quality standards, calibrants, and reference materials are a prerequisite for valid results in any such analysis.

Among the regulated Mycotoxins offered by Fermentek are: Aflatoxin B1, B2, G1, G2, M1, M2, Aflatoxicol, Aphidicolin, Citrinin, Cytochalasin, Deoxynivalenol (DON), HT-2 toxin, Fumonisin, Fusarenon X, Gliotoxin, Nivalenol, Ochratoxin, Patulin, Sterigmatocystin, T2 Toxin, Tentoxin, and Zearalenone.

Cytochalasin D

Cytochalasin D
Molecular Formula
C30H37NO6
M.W.
507.62
CAS number
22144-77-0
MSDS
Source
Zygosporium mansonii
Fermentek product Code
CYD-001
Brand/grade
For research
Appearance
White powder
Purity by HPLC
≥97% ; refer to CoA for more data
Purity By TLC
≥98% ; refer to CoA for more data
Melting point
230°C-245°C
Solubility test
Clear colorless solution at 25mg/ml DMSO, Clear colorless solution at 5mg/ml Ethanol
Names and identifiers

Synonyms: Zygosporin A

Chemical Name: (7S,13E,16S,18R,19E,21R)-21-(Acetyloxy)- 7,18-dihydroxy-16,18-dimethyl-10-phenyl[11]cytochalasa-6(12),13,19-triene-1,17-dione

EU number
244-804-1
Description

Cytochalasin D is a cell permeable mycotoxin, which causes both the association and dissociation of actin subunits. Cytochalasin D disrupts actin filaments and inhibits actin polymerization.

InChl Key
SDZRWUKZFQQKKV-JHADDHBZSA-N
Canonical SMILES
CC1CC=CC2C(C(=C)C(C3C2(C(C=CC(C1=O)(C)O)OC(=O)C)C(=O)NC3CC4=CC=CC=C4)C)O
Isomeric SMILES
C[C@H]1C/C=C/[C@H]2[C@@H](C(=C)[C@H]([C@@H]3[C@@]2([C@@H](/C=C/[C@@](C1=O)(C)O)OC(=O)C)C(=O)N[C@H]3CC4=CC=CC=C4)C)O
Solubility ( literature )

DMSO, Ethanol, Methanol

Compound Classification
  • Macrolide indol mycotoxin
  • Cytochalasin
  • Actin inhibitor
Storage, handling
Store in a freezer upon arrival, at -10°C to -25°C
Protect from moisture
Open carefully.
Use the original container to store the product.
Avoid exposing to strong direct light.
Store under argon.
Other vendors may recommend higher temperatures for storage.
Retest time
3 Years
Applications

Cytochalasins are used as tools in cytological research, and in the field of actin polymerization. Cytochalasin D is 10 times more effective than cytochalasin B and does not inhibit glucose transport across cell membranes.

Disclaimer
For Research use only
Not for Human or Drug use
Not extracted from humans or animals
Refer to MSDS for further safety and handling instructions
Ingredient type
Fermentek product
Available since
Title
Deleted CAS Numbers
Value
11032-97-6 ; 25852-72-6 ; 28455-04-1 ; 69401-32-7
Title
TSE
Value
V
Title
sig
Value
250255
Signal to sort
C

Cytochalasin C

Cytochalasin C
Molecular Formula
C30H37NO6
M.W.
507.62
CAS number
22144-76-9
MSDS
Source
Metarhizium anisopliae
Fermentek product Code
CYC-001
Brand/grade
For research
Appearance
White powder
Purity by HPLC
≥98% ; refer to CoA for more data
Purity By TLC
≥98% ; refer to CoA for more data
Melting point
265°C-280°C
Solubility test
Clear colorless solution at 5mg/ml Dichloromethane
Names and identifiers

RTECS: HA5300500

EU number
244-803-6
Description

A fungal metabolite that acts as a potent inhibitor of actin filament and contractile microfilaments.

InChl Key
NAIODHJWOHMDJX-BBXOWAOSSA-N
Canonical SMILES
CC1CC=CC2C(C(=C(C3C2(C(C=CC(C1=O)(C)O)OC(=O)C)C(=O)NC3CC4=CC=CC=C4)C)C)O
Isomeric SMILES
CC1C/C=C/C2C(C(=C(C3C2(C(/C=C/C(C1=O)(C)O)OC(=O)C)C(=O)NC3CC4=CC=CC=C4)C)C)O
Solubility ( literature )

Dichloromethane , Ethyl acetate

Compound Classification

Macrolide indol mycotoxinCytochalasinActin inhibitor

Storage, handling
-20°C. Protect from light.
Retest time
3 Years
Applications

Cytochalasins are used as tools in cytological research, and in the field of actin polymerisation

Disclaimer
For Research use only
Not for Human or Drug use
Not extracted from humans or animals
Refer to MSDS for further safety and handling instructions
Ingredient type
Fermentek product
Available since

Cytochalasin B

Cytochalasin B
Molecular Formula
C29H37NO5
M.W.
479.61
CAS number
14930-96-2
MSDS
Source
Drechslera dematoidea
Fermentek product Code
CYB-001
Brand/grade
For research
Appearance
White to off-white powder
Purity by HPLC
≥98% ; refer to CoA for more data
Purity By TLC
≥98% ; refer to CoA for more data
Melting point
215°C-226°C
Solubility test
Clear colorless solution at 20 mg/ml Methanol or DMSO
Names and identifiers

Synonyms: Phomin

RTECS: RO0205000

EU number
239-000-2
Description

Mycotoxin capable of interfering microfilament formation.

InChl Key
MAARMMDZGR-IYKJBVLXSA-N
Canonical SMILES
CC1CCCC(C=CC(=O)OC23C(C=CC1)C(C(=C)C(C2C(NC3=O)CC4=CC=CC=C4)C)O)O
Isomeric SMILES
C[C@@H]1CCC[C@@H](/C=C/C(=O)O[C@]23[C@@H](/C=C/C1)[C@@H](C(=C)[C@H]([C@H]2[C@@H](NC3=O)CC4=CC=CC=C4)C)O)O
Solubility ( literature )

DMSO or Ethanol.

Compound Classification

Macrolide indol mycotoxin

Cytochalasin

Actin inhibitor

Storage, handling
Store in a freezer upon arrival, at -10°C to -25°C
Protect from moisture
Use the original container to store the product.
Keep the lid tightly closed.
Avoid exposing to strong direct light.
Other vendors may recommend higher temperatures for storage.
Retest time
3 Years
Applications

Inhibits cell division by interfering with the formation of contractile microfilaments. Inhibits cell movement and induces nuclear extrusion. Interferes with actin polymerization. Inhibits glucose transport

Disclaimer
For Research use only
Not for Human or Drug use
Not extracted from humans or animals
Refer to MSDS for further safety and handling instructions
Ingredient type
Fermentek product
Available since
Title
TSE
Value
P
Title
Transport information
Value
PgII
Title
Deleted CAS numbers
Value
11032-95-4; 11042-65-2; 16006-03-4; 21476-12-0
Title
REACH status
Value
On REACH List of Pre-Registered Substances, March 2009 Registration Date: 31-MAY-2013. On EINECS Annex to June 1990
Signal to sort
C

Cytochalasin A

Cytochalasin A
Molecular Formula
C29H35NO5
M.W.
477.59
CAS number
14110-64-6
MSDS
Source
Drechslera dematoidea
Fermentek product Code
CYA-001
Brand/grade
For research
Appearance
White powder
Purity by HPLC
≥98% ; refer to CoA for more data
Purity By TLC
≥98% ; refer to CoA for more data
Melting point
185°C-193°C
Solubility test
Clear colorless solution at 10mg/ml Dichloromethane
EU number
237-964-9
Description

Cytochalasin A is a fungal toxin which inhibits glucose transport, actine polymerization and blocks the formation of microtubuli. Inhibits cell division. Inhibits HIV-1 protease

InChl Key
ZMAODHOXRBLOQO-TZVKRXPSSA-N
Canonical SMILES
CC1CCCC(=O)C=CC(=O)OC23C(C=CC1)C(C(=C)C(C2C(NC3=O)CC4=CC=CC=C4)C)O
Isomeric SMILES
C[C@@H]1CCCC(=O)/C=C/C(=O)O[C@]23[C@@H](/C=C/C1)[C@@H](C(=C)[C@H]([C@H]2[C@@H](NC3=O)CC4=CC=CC=C4)C)O
Solubility ( literature )

DMSO, Acetone, Ethanol.

Compound Classification

Macrolide indol mycotoxinCytochalasinActin inhibitor

Storage, handling
Store in a freezer upon arrival, at -10°C to -25°C
Avoid exposing to strong direct light.
Other vendors may recommend higher temperatures for storage.
Retest time
3 Years
Applications

Cytochalasins are used as tools in cytological research, and in the field of actin polymerization

Disclaimer
For Research use only
Not for Human or Drug use
Not extracted from humans or animals
Refer to MSDS for further safety and handling instructions
Ingredient type
Fermentek product
Available since

Cyclopiazonic acid

Cyclopiazonic acid
Molecular Formula
C20H20N2O3
M.W.
336.38
CAS number
18172-33-3
Source
Penicillium griseofulvum
Fermentek product Code
CPA-001
Brand/grade
For research
Appearance
Off white to faint yellow powder
Purity by HPLC
≥98% ; refer to CoA for more data
Purity By TLC
≥98% ; refer to CoA for more data
Solubility test
Clear bright yellow solution at 10mg/ml Dichloromethane; Clear bright yellow solution at 100mM DMSO
Names and identifiers

RTECS: UY8587000

EU number
634-041-6
Description

Cyclopiazonic acid (aka CPA) is a toxic compound of indole tetramic acid group. This mycotoxin is produced by Penicillium and Aspergillus fungi.  CPA inhibits SERCA (sarcoplasmic or endoplasmic reticulum calcium-dependent ATPase and thus interferes with the muscle contraction-relaxation cycle.

InChl Key
SZINUGQCTHLQAZ-UHFFFAOYSA-N
Canonical SMILES
CC(=O)C1=C(C2C3C(CC4=C5C3=CNC5=CC=C4)C(N2C1=O)(C)C)O
Solubility ( literature )

DMSO, Methylene Chloride and Methanol.

Compound Classification

Bioactivity:

  • tremorgen mycotoxin
  • vasodilator
  • endoplasmic reticulum inhibitor
Storage, handling
-20°C.
Retest time
3 Years
Applications

Cyclopiazonic acid is a reversible inhibitor of endoplasmic reticulum Ca++ATPase

Ingredient type
Fermentek product
Available since
Title
TSE
Value
F
Title
sig
Value
239805
Title
Transport information
Value
PG II
Signal to sort
C

Citrinin

Citrinin
Molecular Formula
C13H14O5
M.W.
250.25
CAS number
518-75-2
MSDS
Source
Penicillium citrinum
Fermentek product Code
CIT-001
Brand/grade
For research
Appearance
Yellow crystalline solid
Purity by HPLC
≥98% ; refer to CoA for more data
Purity By TLC
≥98% ; refer to CoA for more data
Solubility test
Clear yellow solution at 10mg/ml Dichloromethane
Names and identifiers

IUPAC Name           (3R,4S)-8-Hydroxy-3,4,5-trimethyl-6-oxo-4,6-dihydro-3H-isochromene-7-carboxylic acid

RTECS DJ2275000  

EU number
208-257-2
Description

Citrinin is a mycotoxin capable of inducing mitochondrial permeability transition. Citrinin also inhibits microtubule polymerization

InChl Key
CBGDIJWINPWWJW-IYSWYEEDSA-N
Canonical SMILES
CC1C(OC=C2C1=C(C(=C(C2=O)C(=O)O)O)C)C
Isomeric SMILES
C[C@@H]1[C@H](OC=C2C1=C(C(=C(C2=O)C(=O)O)O)C)C
Solubility ( literature )

Slightly soluble in water. Soluble in dilute alkaline solutions. Soluble in methanol, ethanol, acetonitrile

Compound Classification

Benzopyran mycotoxin

Apoptosis inducer

Storage, handling
Store in a freezer upon arrival, at -10°C to -25°C
Hygroscopic substance.
Protect from moisture
Use the original container to store the product.
Keep the lid tightly closed.
Avoid exposing to strong direct light.
Open carefully – Lyophilized solid under vacuum
Retest time
3 Years
Applications

Initially isolated as a broad-spectrum antibiotic.

Disclaimer
For Research use only
Not for Human or Drug use
Not extracted from humans or animals
Refer to MSDS for further safety and handling instructions
Ingredient type
Fermentek product
Available since
Title
Deleted CAS Numbers
Value
11003-17-1; 16051-41-5
Title
Transport information
Value
Pg III
Title
CN code
Value
29419000
Title
Annex III inventory
Value
# Suspected carcinogen: The Toolbox profiler Carcinogenicity (genotox and nongenotox) alerts by ISS gives an alert for carcinogenicity; CAESAR Carcinogenicity model in VEGA (Q)SAR platform predicts that the chemical is Carcinogen (moderate reliability); I
Title
REACH status
Value
These pre-registration intentions were submitted to ECHA between 1 June and 1 December 2008
Signal to sort
C

Citreoviridin

Citreoviridin
Molecular Formula
C23H30O6
M.W.
402.48
CAS number
25425-12-1
Source
Penicillium sp.
Fermentek product Code
CIR-001
Brand/grade
For research
Appearance
Yellow to Orange-yellow powder
Purity by HPLC
≥95% ; refer to CoA for more data
Purity By TLC
≥98% ; refer to CoA for more data
Melting point
107°C-112°C
Solubility test
Clear yellow solution at 10mg/ml of DMSO, Methanol or Dichloromethane
Names and identifiers

Synonyms

  • Citreoviridin A
  • 4-Methoxy-5-methyl-6-(7-methyl-8-(tetrahydro-3,4-dihydroxy-2,4,5-trimethyl-2-furyl)-1,3,5,7-octatetraenyl)-2H-pyran-2-one
  • IUPAC Name: 6-[(1E,3E,5E,7E)-8-[(2S,3R,4R,5R)-3,4-Dihydroxy-2,4,5-trimethyloxolan-2-yl]-7-methylocta-1,3,5,7-tetraenyl]-4-methoxy-5-methylpyran-2-one

 RTECSUQ1235000

EU number
636-737-5
Chemical name
Citreoviridin
Description

Citreoviridin is a neurotoxic mycotoxin from Penicillium citeoviride, Penicillium toxicarium, Penicillium ochrosalmoneum, Penicillium ochrosalmoneum, Aspergillus terreus, and several other related fungi. Citreoviridin is believed to be the cause of the Acute Cardiac Beri-Beri disease. Naturally, It is formed on rice improperly stored.

InChl Key
JLSVDPQAIKFBTO-OMCRQDLASA-N
Canonical SMILES
CC1C(C(C(O1)(C)C=C(C)C=CC=CC=CC2=C(C(=CC(=O)O2)OC)C)O)(C)O
Isomeric SMILES
C[C@@H]1[C@]([C@H]([C@](O1)(C)/C=C(\C)/C=C/C=C/C=C/C2=C(C(=CC(=O)O2)OC)C)O)(C)O
Solubility ( literature )

Citreoviridin is soluble in benzene, ethanol, chloroform, ether, dichloromethane. Citreoviridin is hardly soluble in water (enough to give it yellow color) and hexane

Compound Classification

Aurovertin class mycotoxin

Comment: Aurovertins are very toxic and complex pyrone derivatives of fungal origin . They bind to and inhibit mitochondrial ATPase, thereby uncoupling oxidative phosphorylation. They are used as biochemical tools.

Storage, handling
Store in a freezer upon arrival, at -10°C to -25°C
Hygroscopic substance.
Protect from moisture
Protect from light !
Open carefully.
Use the original container to store the product.
Keep the lid tightly closed.
Store under argon.
Other vendors may recommend higher temperatures for storage.
Retest time
2 Years
Applications

As other Aurovertin group members, Citreoviridin binds to and inhibit mitochondrial ATPase, thereby uncoupling oxidative phosphorylation.

Citreoviridin, a mycotoxin that has been shown to inhibit the mitochondrial ATP synthetase system. It inhibits soluble ATPase, ADP-stimulated respiration in isolated rat liver mitochondria, and ATP-driven reduction of NAD+ by succinate (KD = 2 µM). Citreoviridin has been used to target ectopic ATPase activity in cancer cells in order to modulate the metabolic activity associated with tumorigenesis.

Disclaimer
For Research use only
Not for Human or Drug use
Not extracted from humans or animals
Refer to MSDS for further safety and handling instructions
Warnings
Ingredient type
Fermentek product
Available since
Title
Transport information
Value
Pg II
Signal to sort
C

Beauvericin

Beauvericin
Molecular Formula
C45H57N3O9
M.W.
783.95
CAS number
26048-05-5
Source
Beauveria bassiana
Fermentek product Code
BEA-001
Brand/grade
For research
Appearance
white crystalline powder
Purity by HPLC
≥98% ; refer to CoA for more data
Purity By TLC
≥98% ; refer to CoA for more data
Melting point
147°C-152°C
Solubility test
Clear colorless solution at 1mg/ml of Methanol; Clear colorless solution at 1mg/ml of Acetonitrile
Description

Beauvericin is a mycotoxin derived from the mould Beauveria bassiana, Fusarium strains and other moulds. Beauvericin belongs to the enniatin family of antibiotics. Beauvericin is a cyclic hexadepsipeptide with alternating L-N-methylphenylalanyl and D-a-hydroxyisovaleryl residues. While being toxic to insects, it is quite harmless for humans.

InChl Key
GYSCAQFHASJXRS-FFCOJMSVSA-N
Canonical SMILES
CC(C)C1C(=O)N(C(C(=O)OC(C(=O)N(C(C(=O)OC(C(=O)N(C(C(=O)O1)CC2=CC=CC=C2)C)C(C)C)CC3=CC=CC=C3)C)C(C)C)CC4=CC=CC=C4)C
Isomeric SMILES
CC(C)[C@@H]1C(=O)N([C@H](C(=O)O[C@@H](C(=O)N([C@H](C(=O)O[C@@H](C(=O)N([C@H](C(=O)O1)CC2=CC=CC=C2)C)C(C)C)CC3=CC=CC=C3)C)C(C)C)CC4=CC=CC=C4)C
Solubility ( literature )

Beauvericin insoluble in water but soluble in organic solvents

Compound Classification

Oligopeptide, ionophore, antibiotic

Storage, handling
Deep frozen (-15 oC to - 20 oC)
Retest time
3 Years
Applications

Beauvericin is active against Gram+ bacteria, mycobacteria, insects, brine shrimp. Beauvericin shows cytotoxic, Immunosuppressant, and apoptotic activity. Beauvericin is the most potent specific inhibitor of cholesterol acyltransferase and possesses ionophoric properties. Beauvericin increases ion permeability in biological membranes by forming a complex with essential cations (Ca2+, Na+, K+), which may affect the ionic homeostasis.

Ingredient type
Fermentek product
Available since
Title
Transport information
Value
Not hazardous for transport
Signal to sort
B

Alternariol monomethyl ether

Alternariol monomethyl ether
Molecular Formula
C15H12O5
M.W.
272.25
CAS number
23452-05-3
MSDS
Source
Alternaria alternata
Fermentek product Code
AME-001
Brand/grade
For research
Appearance
Off-white to light pink powder
Purity by HPLC
≥98% ; refer to CoA for more data
Purity By TLC
≥98% ; refer to CoA for more data
Melting point
255°C-270°C
Solubility test
Clear colorless solution at 1mg/ml Acetone.
Clear colorless solution at 1mg/ml Methanol (slight heating).
Names and identifiers

Alternate names

  • AME
  • Djalonensone
  • Alternariol monomethyl ether
  • Alternariol methyl ether
  • Alternariol-9-methyl ether

RTECS : HP8755000

EU number
636-657-0
Description

Alternariol monomethyl ether (AME) is a natural mycotoxin originated in Alternaria alternata fungi . It inhibits  Cholinesterase, and posesses  antifungal and phytotoxic properties.

InChl Key
LCSDQFNUYFTXMT-UHFFFAOYSA-N
Canonical SMILES
CC1=CC(=CC2=C1C3=CC(=CC(=C3C(=O)O2)O)OC)O
Solubility ( literature )

Soluble in DMSO, pure ethanol, methanol

Compound Classification

Pyrrolidinone mycotoxin

 

Storage, handling
Store in a freezer upon arrival, at -10°C to -25°C
Retest time
3 Years
Disclaimer
For Research use only
Not for Human or Drug use
Not extracted from humans or animals
Refer to MSDS for further safety and handling instructions
Ingredient type
Fermentek product
Non hazardous for shipment.
Available since
Title
Transport information
Value
Not hazardous for transport
Title
CAS number validated
Value
26894-49-5; 641-38-3
Title
Deleted CAS Numbers
Value
31273-73-1; 916665-00-4; 11003-13-7
Signal to sort
A

Alternariol

Alternariol
Molecular Formula
C14H10O5
M.W.
258.23
CAS number
641-38-3
Source
Alternaria alternata
Fermentek product Code
ALR-001
Brand/grade
For research
Appearance
Off white to slight yellow to slight pink powder
Purity by HPLC
≥98% ; refer to CoA for more data
Purity By TLC
≥98% ; refer to CoA for more data
Melting point
340°C-350°C (decompos.)
Solubility test
Clear colorless solution at 5mg/ml Acetone; Clear colorless solution at 5mg/ml Methanol
Names and identifiers

Synonyms:

  • AOH

Systematic Name :3,7,9-Trihydroxy-1-methyl-6H-dibenzo[b,d]pyran-6-on

RTECS: HP8757000

 

EU number
636-339-1
Description

Alternariol is a mycotoxin that contaminates fruit and cereals. It is named after the fungal genus Alternaria. Alternariol shows anti-fungal and phytotoxic activity. Alternariol inhibits cholinesterase.

InChl Key
CEBXXEKPIIDJHL-UHFFFAOYSA-N
Canonical SMILES
CC1=CC(=CC2=C1C3=CC(=CC(=C3C(=O)O2)O)O)O
Solubility ( literature )

Soluble in DMSO, pure ethanol, methanol

Compound Classification

Pyrrolidinone mycotoxin

Storage, handling
Store in a freezer upon arrival, at -10°C to -25°C
Hygroscopic substance.
Protect from moisture
Use the original container to store the product.
Keep the lid tightly closed.
Avoid exposing to strong direct light.
Other vendors may recommend storing under argon
Retest time
3 Years
Disclaimer
For Research use only
Not for Human or Drug use
Not extracted from humans or animals
Refer to MSDS for further safety and handling instructions
Ingredient type
Fermentek product
Available since
Title
Deleted CAS Numbers
Value
11003-13-7
Title
Transport information
Value
Pg III
Signal to sort
A