Warning or harmful

  • Acute toxicity (oral, dermal, inhalation), category 4
  • Skin irritation, categories 2, 3
  • Eye irritation, category 2A
  • Skin sensitization, category 1
  • Specific target organ toxicity following single exposure, category 3
    • Respiratory tract irritation
    • Narcotic effects

Standard solution T2 and HT toxins

Standard solution T2 and HT toxins
MSDS
Fermentek product Code
SSTH
Brand/grade
Analytical standard
Names and identifiers

Synonyms:

Chemical names:

IUPAC:

RTECS#

Storage, handling
Store in a freezer upon arrival, at -10°C to -25°C
Open carefully.
Use the original container to store the product.
Keep the lid tightly closed.
Other vendors may recommend higher temperatures for storage.
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

Warning or harmful

  • Acute toxicity (oral, dermal, inhalation), category 4
  • Skin irritation, categories 2, 3
  • Eye irritation, category 2A
  • Skin sensitization, category 1
  • Specific target organ toxicity following single exposure, category 3
    • Respiratory tract irritation
    • Narcotic effects
Ingredient Reference
T2 Toxin
Ingredient type
Fermentek product
Ingredient amount
100 PPM
Ingredient Reference
HT2 toxin
Ingredient type
Fermentek product
Ingredient amount
100 PPM
Ingredient Other
Acetonitrile (HPLC grade Supra-gradient)
Ingredient type
Fermentek product
Ingredient amount
100%
Ingredient type
Fermentek product
Customs: Laboratory reagents-38220000
Available since
Fermentek Product Category
Standard Solutions
Signal to sort
S

Wilforlide A

Wilforlide A
Molecular Formula
C30H46O3
M.W.
454.68
CAS number
84104-71-2
Source
Tripterygium wilfordii
Fermentek product Code
WIL-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
315°C-321°C
Solubility test
Clear colorless solution at 10mg/ml of Methanol
Names and identifiers

Synonyms:

  • Wilforlide A
  • Regelide
  • Abruslactone A

Chemical names:

(2S,5S,5aR,7aS,7bR,9aR,11S,13aR,13bR,15bS)-11-hydroxy-2,5a,7a,7b,10,10,13a-heptamethyl-1,5,5a,6,7,7a,7b,8,9,9a,10,11,12,13,13a,13b,14,15b-octadecahydro-2,5-methanochryseno[2,1-c]oxepin-3(2H)-one

Synonym: Wilforlide A; Regelide; Abruslactone A

IUPAC: (3β,22α)-3-Hydroxy-22,29-epoxyolean-12-en-29-one 

RTECS#

EU number
683-224-7
InChl Key
HHQJBWYXBWOFJY-YLXTXNMFSA-N
Canonical SMILES
CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC6(CC5OC6=O)C)C)C)C)C
Isomeric SMILES
C[C@]12CC[C@@H](C([C@@H]1CC[C@@]3([C@@H]2CC=C4[C@]3(CC[C@@]5([C@H]4C[C@]6(C[C@@H]5OC6=O)C)C)C)C)(C)C)O
Storage, handling
Store in a freezer upon arrival, at -10°C to -25°C
Open carefully.
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.
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

NotAnimal

No animal ingredients

NotGMO

Product natural

Health-Hazard

  • Respiratory sensitization, category 1
  • Germ cell mutagenicity, categories 1A, 1B, 2
  • Carcinogenicity, categories 1A, 1B, 2
  • Reproductive toxicity, categories 1A, 1B, 2
  • Specific target organ toxicity following single exposure, categories 1, 2
  • Specific target organ toxicity following repeated exposure, categories 1, 2
  • Aspiration hazard, categories 1, 2

Warning or harmful

  • Acute toxicity (oral, dermal, inhalation), category 4
  • Skin irritation, categories 2, 3
  • Eye irritation, category 2A
  • Skin sensitization, category 1
  • Specific target organ toxicity following single exposure, category 3
    • Respiratory tract irritation
    • Narcotic effects

Corrosive

  • Skin corrosion, categories 1A, 1B, 1C
  • Serious eye damage, category 1
Ingredient type
Fermentek product
Shipped at ambient temperature
Shipped in PP / PE bottle.
Available since
Title
lit1
Value
Appearance: Solid powder Purity: >98% (or refer to the Certificate of Analysis) Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Custo
Title
lit2
Value
Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years). Solubility: Soluble in DMSO Shelf Life: >3 years if stored properly Drug Formulation: This drug may be formulated in DMSO Stock Solution S
Fermentek Product Category
Plant-derived
Signal to sort
W

Quote for

Price
$100.00

Tropodithietic acid (TDA)

Tropodithietic acid (TDA)
Molecular Formula
C8H4O3S2
M.W.
212.25
CAS number
750590-18-2
Source
Phaeobacter gallaeciensis
Fermentek product Code
TDA-001
Brand/grade
For research
Appearance
Orange powder
Purity by HPLC
≥98% ; refer to CoA for more data
Purity By TLC
≥98% ; refer to CoA for more data
Melting point
207°C-213°C
Solubility test
Clear yellow solution at 1 mg/ml of Dichloromethane.
Clear yellow solution at 0.5 mg/ml of Methanol
Names and identifiers

Synonyms:             TDA

Chemical names:   Tropodithietic acid

IUPAC:                    3-Oxo-8,9-dithiabicyclo[5.2.0]nona-1,4,6-triene-2-carboxylic acid

RTECS#                   Not available

 

EU number
806-061-7
Chemical name
Tropodithietic acid
Description

A sulphur containing antibiotic from marine bacteria, responsible for the probiotic proprties of some of these.  Tropodithietic acid It is active against Gram-positive and Gram-negative bacteria, some phytopathogens and mycoplasma. It also has anti-plasmodium activity.

InChl Key
BLFCMITWMARUSM-UHFFFAOYSA-N
Canonical SMILES
C1=CC(=O)C(=C2C(=C1)SS2)C(=O)O
Solubility ( literature )

Soluble in polar organic solvents, such as DMSO, Methanol, Acetone

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.
Keep the lid tightly closed.
Avoid exposing to strong direct light.
Other vendors may recommend higher temperatures for storage.
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

Warning or harmful

  • Acute toxicity (oral, dermal, inhalation), category 4
  • Skin irritation, categories 2, 3
  • Eye irritation, category 2A
  • Skin sensitization, category 1
  • Specific target organ toxicity following single exposure, category 3
    • Respiratory tract irritation
    • Narcotic effects
Ingredient type
Fermentek product
Available since
Title
Transport information
Value
Not hazardous for transport
Title
source
Value
Phaeobacter gallaeciensis
Fermentek Product Category
Antibiotics
Research field: Cancer
Apoptosis related
Anti Protozoal
Anti Bacterial
Signal to sort
T

Quote for

Price
$100.00

Zearalenone

Zearalenone
Molecular Formula
C18H22O5
M.W.
318.36
CAS number
17924-92-4
MSDS
Source
Giberella zeae
Fermentek product Code
ZRE-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
159°C-166°C
Solubility test
Clear colourless solution at 5mg/ml of Methanol
Names and identifiers

IUPAC : (3S,11E)-14,16-dihydroxy-3-methyl-3,4,5,6,9,10-hexahydro-1H-2-benzoxacyclotetradecine-1,7(8H)-dione

RTECS: DM2550000

EU number
241-864-0
Description

Zearalenone is a natural estrogen, a mycotoxin from resorcylic acid lactone group. 

Zearalenone is a non-steroidal estrogenic mycotoxin produced by
several Fusarium spp. It has been implicated in numerous
mycotoxicoses in farm animals, especially in pigs. Zearalenone is
heat-stable and is found worldwide in a number of cereal crops, such
as maize, barley, oats, wheat, rice, and sorghum (Kuiper-Goodman et
al., 1987; Tanaka et al., 1988a) and also in bread (Aziz et al.,
1997). Zearalenone was shown to be produced on corn by Fusarium
isolates from Australia, Europe, and North America (Vesonder et al.,
1991) and in New Zealand (diMenna et al., 1997), the Philippines,
Thailand, and Indonesia (Yamashita et al., 1995). The occurrence of
zearalenone in food and feed was also demonstrated in South America
(Dalcero et al., 1997; Molto et al., 1997), Africa (Doko et al.,
1996), China and the former USSR (Ueno et al., 1986). Fusarium
isolates from bananas can also produce zearalenone

InChl Key
MBMQEIFVQACCCH-QBODLPLBSA-N
Canonical SMILES
CC1CCCC(=O)CCCC=CC2=CC(=CC(=C2C(=O)O1)O)O
Isomeric SMILES
C[C@H]1CCCC(=O)CCC/C=C/C2=CC(=CC(=C2C(=O)O1)O)O
Solubility ( literature )

Zearalenone is slightly soluble in hexane and progressively more in benzene, acetonitrile, dichloromethane, methanol, acetone. In water: 20 mg/L .

Compound Classification
  • Mycotoxin
  • A resorcylic acid lactone
  •  
  •  
  • Sexual reproduction in Fusarium is regulated by the fungal sex hormone zearalenone, which is known to be synthesized only by species of Gibberella zeae (Fusarium roseum)

 

Storage, handling
Store in a freezer upon arrival, at -10°C to -25°C
Keep the lid tightly closed.
Avoid exposing to strong direct light.
Other vendors may recommend higher temperatures for storage.
Applications

The resorcylic acid lactones have estrogenic activity. Zearalenone and its derivates were used as veterinary anabolic or estrogen substitutes.

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
Not for veterinary use!
Warnings

Warning or harmful

  • Acute toxicity (oral, dermal, inhalation), category 4
  • Skin irritation, categories 2, 3
  • Eye irritation, category 2A
  • Skin sensitization, category 1
  • Specific target organ toxicity following single exposure, category 3
    • Respiratory tract irritation
    • Narcotic effects

Corrosive

  • Skin corrosion, categories 1A, 1B, 1C
  • Serious eye damage, category 1
Ingredient type
Fermentek product
Available since
Title
Transport information
Value
Not hazardous for transport
Fermentek Product Category
Mycotoxins
Other mycotoxins
Signal to sort
Z

Quote for

Price
$1.00

Verruculogen

Verruculogen
Molecular Formula
C27H33N3O7
M.W.
511.57
CAS number
12771-72-1
Source
Penicillium simplicissimum
Fermentek product Code
VRR-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
227°C -233°C
Names and identifiers

IUPAC NAME:

(5S,10S,10aR,14aS,15bS)-10,10a-Dihydroxy-7-methoxy-2,2-dimethyl-5-(2-methyl-1-propen-1-yl)-1,10,10a,14,14a,15b-hexahydro-12H-3,4-dioxa-5a,11a,15a-triazacycloocta[1,2,3-lm]indeno[5,6-b]fluorene-11,15(2 H,13H)-dione

 

EU number
634-189-1
Description

Verruculogen is a tremorgenic mycotoxin, affecting CNS functions, arresting mammary carcinoma cells in vitro, affecting potassium channels. Verruculogen decreases GABA levels in CNS. Tremorgenic doses of verruculogen increase the number and decrease the affinity of DHP receptors in rat cortex. Verruculogen is a potent inhibitor of high conductance Ca activated K (maxi-K) channel.

InChl Key
LRXYHMMJJCTUMY-KZXQSYCZSA-N
Canonical SMILES
CC(=CC1N2C3=C(C=CC(=C3)OC)C4=C2C(CC(OO1)(C)C)N5C(=O)C6CCCN6C(=O)C5(C4O)O)C
Isomeric SMILES
CC(=C[C@H]1N2C3=C(C=CC(=C3)OC)C4=C2[C@H](CC(OO1)(C)C)N5C(=O)[C@@H]6CCCN6C(=O)[C@@]5([C@H]4O)O)C
Solubility ( literature )

Soluble in benzene, ethyl acetate, and acetone; slightly soluble in ethanol; very soluble in CHCI;

Compound Classification

Tremorgenic neurotoxin affecting central neural system.

Storage, handling
Store in a freezer upon arrival, at -10°C to -25°C
Use the original container to store the product.
Keep the lid tightly closed.
Avoid exposing to strong direct light.
Protect from moisture! Hygroscopic substance.
Applications

Verruculogen decreases GABA levels in CNS. Tremorgenic doses of verruculogen increase the number and decrease the affinity of DHP receptors in rat cortex.Verruculogen is a potent inhibitor of high conductance Ca activated K (maxi-K) channel.

Disclaimer
For Research use only.
Warnings

Warning or harmful

  • Acute toxicity (oral, dermal, inhalation), category 4
  • Skin irritation, categories 2, 3
  • Eye irritation, category 2A
  • Skin sensitization, category 1
  • Specific target organ toxicity following single exposure, category 3
    • Respiratory tract irritation
    • Narcotic effects
Ingredient type
Fermentek product
Available since
Title
Transport information
Value
Not hazardous for transport
Fermentek Product Category
Mycotoxins
Tremorgens
Signal to sort
V

Quote for

Price
$1.00

Sterigmatocystin

Sterigmatocystin
Molecular Formula
C18H12O6
M.W.
324.28
CAS number
10048-13-2
MSDS
Source
Aspergillus versicolor
Fermentek product Code
STR-001
Brand/grade
For research
Appearance
Yellow to slight yellow powder
Purity by HPLC
≥98% ; refer to CoA for more data
Purity By TLC
≥98% ; refer to CoA for more data
Melting point
240°C-246°C
Solubility test
Clear colorless solution at 5mg/ml of Acetone; Clear colorless solution at 10mg/ml of DMSO
Names and identifiers

Systematic name:    8-Hydroxy-6-methoxy-3a,12c-dihydro-7H-furo[3',2':4,5]furo[2,3-c]xanthen-7-one

RTECS:                     LV1750000

RTECS#:                 LV1750000

HSDB:                      HSDB3540

EU number
233-158-6
Description

Sterigmatocystin is a mycotoxin, inhibitor of DNA synthesis, closely related to Aflatoxins.

InChl Key
UTSVPXMQSFGQTM-DCXZOGHSSA-N
Canonical SMILES
COC1=C2C(=C3C4C=COC4OC3=C1)OC5=C(C2=O)C(=CC=C5)O
Isomeric SMILES
COC1=C2C(=C3[C@@H]4C=CO[C@@H]4OC3=C1)OC5=C(C2=O)C(=CC=C5)O
Solubility ( literature )

DMSO, Methanol, Ethanol, Acetone.

Compound Classification

Chemical classification:

Xanthones
    Sterigmatocystin

Bioactivity classification:

Toxin affecting liver and kidneys
Sterigmatocystin

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.
Keep the lid tightly closed.
Avoid exposing to strong direct light.
Other vendors may recommend higher temperatures for storage.
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
Not for veterinary use!
Warnings

Health-Hazard

  • Respiratory sensitization, category 1
  • Germ cell mutagenicity, categories 1A, 1B, 2
  • Carcinogenicity, categories 1A, 1B, 2
  • Reproductive toxicity, categories 1A, 1B, 2
  • Specific target organ toxicity following single exposure, categories 1, 2
  • Specific target organ toxicity following repeated exposure, categories 1, 2
  • Aspiration hazard, categories 1, 2

Warning or harmful

  • Acute toxicity (oral, dermal, inhalation), category 4
  • Skin irritation, categories 2, 3
  • Eye irritation, category 2A
  • Skin sensitization, category 1
  • Specific target organ toxicity following single exposure, category 3
    • Respiratory tract irritation
    • Narcotic effects
Ingredient type
Fermentek product
Transport safety: class 6.1 PG III
Available since
Title
Transport information
Value
Pg III
Title
Deleted CAS numbers
Value
105521-97-9
Fermentek Product Category
Mycotoxins
Aflatoxins
Signal to sort
S

Quote for

Price
$1.00
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