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Merck

90656

Supelco

17α(H),21β(H)-Hopane solution

0.1 mg/mL in isooctane, analytical standard

Synonim(y):

α-Hopan

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About This Item

Wzór empiryczny (zapis Hilla):
C30H52
Numer CAS:
Masa cząsteczkowa:
412.73
Numer WE:
Numer MDL:
Kod UNSPSC:
85151701
Identyfikator substancji w PubChem:
NACRES:
NA.24

klasa czystości

analytical standard

Poziom jakości

okres trwałości

limited shelf life, expiry date on the label

stężenie

0.1 mg/mL in isooctane

metody

HPLC: suitable
gas chromatography (GC): suitable

Zastosowanie

food and beverages

format

single component solution

temp. przechowywania

−20°C

ciąg SMILES

CC(C)[C@H]1CC[C@@]2(C)[C@@H]1CC[C@]3(C)[C@@H]2CC[C@@H]4[C@@]5(C)CCCC(C)(C)[C@@H]5CC[C@@]34C

InChI

1S/C30H52/c1-20(2)21-12-17-27(5)22(21)13-18-29(7)24(27)10-11-25-28(6)16-9-15-26(3,4)23(28)14-19-30(25,29)8/h20-25H,9-19H2,1-8H3/t21-,22-,23+,24-,25-,27+,28+,29-,30-/m1/s1

Klucz InChI

ZRLNBWWGLOPJIC-SUWMKODTSA-N

Powiązane kategorie

Zastosowanie

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

Hasło ostrzegawcze

Danger

Zwroty wskazujące rodzaj zagrożenia

Zwroty wskazujące środki ostrożności

Klasyfikacja zagrożeń

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

Organy docelowe

Central nervous system

Kod klasy składowania

3 - Flammable liquids

Klasa zagrożenia wodnego (WGK)

WGK 2

Temperatura zapłonu (°F)

10.4 °F - closed cup

Temperatura zapłonu (°C)

-12 °C - closed cup

Środki ochrony indywidualnej

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Certyfikaty analizy (CoA)

Lot/Batch Number

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Paula V Welander et al.
Proceedings of the National Academy of Sciences of the United States of America, 107(19), 8537-8542 (2010-04-28)
The rise of atmospheric oxygen has driven environmental change and biological evolution throughout much of Earth's history and was enabled by the evolution of oxygenic photosynthesis in the cyanobacteria. Dating this metabolic innovation using inorganic proxies from sedimentary rocks has
H G M Edwards et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 78(1), 191-195 (2010-11-06)
The aim of this work is to investigate the viability and potential of three groups of organic compounds as biomarkers in a future robotic analytical exploration of Mars. The three compounds have been identified as suitable candidates for potential biomarkers
Li-guo Guo et al.
Huan jing ke xue= Huanjing kexue, 31(8), 1897-1903 (2010-11-26)
Biodegradabilities of several hydrocarbon biomarker groups, including isoprene, hopanes and steranes in a medium-crude oil BZ34-1 and a heavy-crude oil SZ36-1 from offshore, were determined under laboratory conditions. The results of GC-MS analysis showed that isoprene biomarkers such as pristane
J P Sáenz et al.
Geobiology, 10(4), 311-319 (2012-02-15)
Cyanobacteria are key players in the global carbon and nitrogen cycles and are thought to have been responsible for the initial rise of atmospheric oxygen during the Neoarchean. There is evidence that a class of membrane lipids known as hopanoids
Y Subhash et al.
International journal of systematic and evolutionary microbiology, 63(Pt 6), 2338-2343 (2012-11-28)
Strain JC141(T) was isolated from an alkaline soil (pH 8.8) at Mau, Uttar Pradesh, India. Colonies were blue with a metallic sheen; cells stained Gram-negative, and were oxidase- and catalase-positive, but chitinase-negative. Major fatty acids were C16:1ω7c/C16:1ω6c, C16:0 and C18:0

Produkty

We provide high-quality, relevant hopane reference standards to be used as biomarkers for petrochemical oil field remediation and spill analysis.

Nasz zespół naukowców ma doświadczenie we wszystkich obszarach badań, w tym w naukach przyrodniczych, materiałoznawstwie, syntezie chemicznej, chromatografii, analityce i wielu innych dziedzinach.

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