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90656

Supelco

17α(H),21β(H)-Hopane solution

0.1 mg/mL in isooctane, analytical standard

Synonym(s):

α-Hopan

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1 ML
$2,520.00

$2,520.00

Estimated to ship onMay 19, 2025

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1 ML
$2,520.00

About This Item

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

$2,520.00

Estimated to ship onMay 19, 2025

Request a Bulk Order

grade

analytical standard

Quality Level

100

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

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

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

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_germany

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM7183
BCCJ7098
BCCF3737
BCCB4929
BCBZ5981

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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
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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