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40220-U

Supelco

Aldrin solution

certified reference material, 5000 μg/mL in methanol

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About This Item

Empirical Formula (Hill Notation):
C12H8Cl6
CAS Number:
309-00-2
Molecular Weight:
364.91
Beilstein:
2336652
MDL number:
MFCD00135587
UNSPSC Code:
77101502
PubChem Substance ID:
329755956
NACRES:
NA.24

grade

certified reference material
TraceCERT®

product line

TraceCERT®

CofA

current certificate can be downloaded

packaging

ampule of 1 mL

concentration

5000 μg/mL in methanol

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

single component solution

storage temp.

2-8°C

SMILES string

ClC1=C(Cl)[C@]2(Cl)[C@@H]3[C@@H]4C[C@@H](C=C4)[C@@H]3[C@@]1(Cl)C2(Cl)Cl

InChI

1S/C12H8Cl6/c13-8-9(14)11(16)7-5-2-1-4(3-5)6(7)10(8,15)12(11,17)18/h1-2,4-7H,3H2/t4-,5+,6+,7-,10+,11-

InChI key

QBYJBZPUGVGKQQ-SJJAEHHWSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Other Notes

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Legal Information

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

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Flam. Liq. 2 - STOT SE 1

Target Organs

Eyes,Central nervous system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

49.5 °F - closed cup - Solvent

Flash Point(C)

9.7 °C - closed cup - Solvent

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
LRAD1162
LRAC0441
XA13639V
XA13638V
LC06759

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Daibin Yang et al.
Environmental science & technology, 44(5), 1854-1859 (2010-02-11)
alpha-HCH (hexachlorocyclohexane) is chiral and can still be detected in almost all environmental media. In this study, the enantioselective behavior of alpha-HCH in mice (CD1) and quail (Coturnix japonica) was investigated and compared after a single dose of exposure. The
Hans Ragnar Norli et al.
Journal of chromatography. A, 1218(41), 7234-7241 (2011-09-09)
The QuEChERS method developed for 22 organochlorine pesticides (OCPs) and 7-polychlorinated biphenyls (PCBs) in fish tissue involves a simple and efficient freezing technique for removal of lipids. The equipment developed consists of disposable syringes and a freezing block constructed from
Xiao-Yuan Tao et al.
Molecular ecology, 21(17), 4371-4385 (2012-04-21)
Cotton plants accumulate phytotoxins, including gossypol and related sesquiterpene aldehydes, to resist insect herbivores and pathogens. To counteract these defensive plant secondary metabolites, cotton bollworms (Helicoverpa armigera) elevate their production of detoxification enzymes, including cytochrome P450 monooxygenases (P450s). Besides their
Xiaomin Li et al.
Journal of chromatography. A, 1277, 69-75 (2013-01-22)
Identification and quantification of related-structure impurity is a research focus in the purity assessment of organic compounds. Determination of the purity value and uncertainty assessment are also important in the metrological research. A method for the determination of related-structure impurity
Le Kang et al.
Epidemiology (Cambridge, Mass.), 21 Suppl 4, S58-S63 (2011-04-01)
Understanding the health effects associated with environmental chemicals is challenging when individuals have concentrations at or below the laboratory limits of detection as well as when the values may round to zero or are presented in the form of 0
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