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Merck
CN

45453

地乐酚

PESTANAL®, analytical standard

别名:

2-仲丁基-4,6-二硝基酚

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关于此项目

经验公式（希尔记法）:
C10H12N2O5
化学文摘社编号:
88-85-7
分子量:
240.21
NACRES:
NA.24
PubChem Substance ID:
329756747
UNSPSC Code:
41116107
EC Number:
201-861-7
MDL number:
MFCD00024246

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产品名称

地乐酚, PESTANAL®, analytical standard

InChI key

OWZPCEFYPSAJFR-UHFFFAOYSA-N

InChI

1S/C10H12N2O5/c1-3-6(2)8-4-7(11(14)15)5-9(10(8)13)12(16)17/h4-6,13H,3H2,1-2H3

SMILES string

CCC(C)c1cc(cc(c1O)[N+]([O-])=O)[N+]([O-])=O

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

storage temp.

2-8°C

Quality Level

100

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Disclaimer

仅限于专业用户。注意 — 避免接触 — 使用前请阅读说明书。

Application

Dinoseb may be used as a reference standard in the analysis of dinoseb residues in samples of raspberry extract using high performance liquid chromatography coupled with ultraviolet-visible light detector (HPLC-UV).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

General description

This compound is listed in the SVHC (Substances of very high concern) candidate list of ECHA (European Chemicals Agency)

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

signalword

Danger

Hazard Classifications

Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Repr. 1B - Skin Irrit. 2 - Skin Sens. 1

supp_hazards

EUH044

存储类别

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

306.9 °F - closed cup

flash_point_c

152.7 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

法规信息

监管及禁止进口产品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCM0929
BCCH5434
BCBW3273

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High-performance liquid chromatography method for the determination of dinoseb: application to the analysis of residues in raspberries
Szeto.YS and Price.MP
Journal of Agricultural and Food Chemistry, 39, 1614-1617 (1991)
Mark R Viant et al.
Aquatic toxicology (Amsterdam, Netherlands), 76(3-4), 329-342 (2005-11-18)
Changes in metabolism of Japanese medaka (Oryzias latipes) embryos exposed to dinoseb (2-sec-butyl-4,6-dinitrophenol), a substituted dinitrophenol herbicide, were determined by in vivo (31)P NMR, high-pressure liquid chromatography (HPLC)-UV, and (1)H NMR metabolomics. ATP and phosphocreatine (PCr) metabolism were characterized within
Qian Zhang et al.
Journal of hazardous materials, 176(1-3), 1058-1064 (2009-12-26)
A novel and efficient photo-Fenton catalyst of Fe(III)-5-sulfosalicylic acid (ssal) supported on Al(2)O(3) was prepared and characterized by FT-IR and TEM-EDX technique. A detailed investigation of photocatalytic degradation of 2-sec-butyl-4,6-dinitrophenol (DNBP) using this catalyst and H(2)O(2) under solar light irradiation
Mariko Matsumoto et al.
Reproductive toxicology (Elmsford, N.Y.), 29(3), 292-297 (2010-02-06)
This study evaluated the prenatal developmental toxicity of the pesticide 2-sec-butyl-4,6-dinitrophenol (dinoseb). Pregnant rats were given dinoseb by gavage at 0, 8.0 or 10 mg/kg bw/day on days 6-15 of gestation, or in the diet at 0, 120 or 200
Mariko Matsumoto et al.
Environmental toxicology, 23(2), 169-183 (2008-01-25)
In a combined repeated dose toxicity study with reproduction/developmental toxicity screening test, Crj:CD(SD)IGS rats were dosed with dinoseb, 2-sec-butyl-4,6-dinitrophenol, by gavage at 0 (vehicle), 0.78, 2.33, or 7.0 mg/kg bw/day. Six males per group were dosed for a total of
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