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Merck
CN

34138

Supelco

Neosolaniol solution

~100 μg/mL in acetonitrile, analytical standard

Synonym(s):

4β,15-Diacetoxy-3α,8α-dihydroxy-12,13-epoxytrichothec-9-ene, 8-Hydroxydiacetoxyscirpenol solution, NEO

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About This Item

Empirical Formula (Hill Notation):
C19H26O8
CAS Number:
Molecular Weight:
382.40
UNSPSC Code:
85151701
PubChem Substance ID:
NACRES:
NA.24
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grade

analytical standard

shelf life

limited shelf life, expiry date on the label

concentration

~100 μg/mL in acetonitrile

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

cleaning products
cosmetics
food and beverages
personal care

format

single component solution

storage temp.

−20°C

SMILES string

CC(=O)C[C@@H]1[C@@H](O)[C@H]2O[C@@H]3C=C(C)[C@@H](O)C[C@]3(COC(C)=O)[C@]1(C)[C@@]24CO4

InChI

1S/C19H26O8/c1-9-5-13-18(6-12(9)22,7-24-10(2)20)17(4)15(26-11(3)21)14(23)16(27-13)19(17)8-25-19/h5,12-16,22-23H,6-8H2,1-4H3/t12-,13?,14+,15+,16+,17+,18+,19-/m1/s1

InChI key

TVZHDVCTOCZDNE-VUQWXZGYSA-N

General description

Neosolaniol is a group A trichothecene mycotoxin produced by fungi of the Fusarium genus, found in grains used for livestock as well as human consumption products such as bread and cereals.

Application

Neosolaniol solution may be used as an analytical reference standard for the estimation of the analyte in human urine samples using gas chromatography coupled to tandem mass spectrometry (GC-MS/MS).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Analysis Note

purity : ≥96.0% (HPLC)

Pictograms

FlameExclamation mark

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

35.6 °F

Flash Point(C)

2 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

高风险级别生物产品--毒素类产品
危险化学品
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Simultaneous determination of type-A and type-B trichothecenes in barley samples by GC-MS.
Ibanez-Vea M, et al.
Food Control, 22(8), 1428-1434 (2011)
Vipin Kumar Deo et al.
Parasitology international, 72, 101938-101938 (2019-06-16)
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Natacha Mendes et al.
Scientific data, 6, 180307-180307 (2019-02-13)
The dataset enables exploration of higher-order cognitive faculties, self-generated mental experience, and personality features in relation to the intrinsic functional architecture of the brain. We provide multimodal magnetic resonance imaging (MRI) data and a broad set of state and trait
Development of a GC--MS/MS strategy to determine 15 mycotoxins and metabolites in human urine.
Rodriguez-Carrasco Y, et al.
Journal of AOAC (Association of Official Analytical Chemists) International, 128, 125-131 (2014)
Nathalie Gonska et al.
Biomacromolecules, 21(6), 2116-2124 (2020-04-01)
The production of large quantities of artificial spider silk fibers that match the mechanical properties of the native material has turned out to be challenging. Recent advancements in the field make biomimetic spinning approaches an attractive way forward since they

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