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Merck
CN

90656

17α(H),21β(H)-Hopane solution

0.1 mg/mL in isooctane, analytical standard

Synonym(s):

α-Hopan

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About This Item

Empirical Formula (Hill Notation):
C30H52
CAS Number:
13849-96-2
Molecular Weight:
412.73
NACRES:
NA.24
PubChem Substance ID:
329769939
UNSPSC Code:
85151701
EC Number:
208-759-1
MDL number:
MFCD16660343

Key Documents

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Product Name

17α(H),21β(H)-Hopane solution, 0.1 mg/mL in isooctane, analytical standard

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

InChI key

ZRLNBWWGLOPJIC-SUWMKODTSA-N

SMILES string

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

grade

analytical standard

shelf life

limited shelf life, expiry date on the label

concentration

0.1 mg/mL in isooctane

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

food and beverages

format

single component solution

storage temp.

−20°C

Quality Level

100

Related Categories

Application

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

signalword

Danger

Hazard Classifications

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

target_organs

Central nervous system

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

10.4 °F - closed cup

flash_point_c

-12 °C - closed cup

ppe

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

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCP1023
BCCN2543
BCCM7183
BCCJ7098
BCCF3737

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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
Masahiko Isaka et al.
Fungal biology, 115(4-5), 401-405 (2011-05-03)
The insect pathogens in the genus Torrubiella s. lat. were recently divided into new genera based on molecular phylogenetic characters. Isolates collected at various locations in Thailand, were tested for their productivity of a hopane-type triterpene, zeorin (6α,22-dihydroxyhopane), when cultured
S Siljeström et al.
Geobiology, 8(1), 37-44 (2009-11-17)
Steranes and hopanes are organic biomarkers used as indicators for the first appearance of eukaryotes and cyanobacteria on Earth. Oil-bearing fluid inclusions may provide a contamination-free source of Precambrian biomarkers, as the oil has been secluded from the environment since
Jemal Demma et al.
Phytotherapy research : PTR, 27(4), 507-514 (2012-06-01)
An extract of Glinus lotoides, a medicinal plant used in Africa and Asia for various therapeutic purposes, was recently shown to cause DNA damage in vitro. To further explore the potential genotoxicity of this plant, fractionation of the crude extract
Fang Wang et al.
Journal of Asian natural products research, 12(1), 94-97 (2010-04-15)
Phytochemical investigation of the whole plant of Dicranostigma leptopodum (Maxim) Fedde led to the isolation of a new hopane triterpene, dicranostigmone (1), and a known compound, erythrodiol-3-O-palmitate (2). The structure of the new compound (1) was elucidated by various spectroscopic
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Hopane Reference Standards for use as Petrochemical Biomarkers in Oil Field Remediation and Spill Analysis

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

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