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Merck
CN

90656

17α(H),21β(H)-藿烷 溶液

0.1 mg/mL in isooctane, analytical standard

别名:

α-Hopan

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关于此项目

经验公式（希尔记法）:
C30H52
化学文摘社编号:
13849-96-2
分子量:
412.73
NACRES:
NA.24
PubChem Substance ID:
329769939
UNSPSC Code:
85151701
EC Number:
208-759-1
MDL number:
MFCD16660343

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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

相关类别

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

存储类别

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

法规信息

危险化学品
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历史批次信息供参考:

分析证书(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
Andrew T Lambe et al.
Environmental science & technology, 43(23), 8794-8800 (2009-12-01)
Hydroxyl radical (OH) uptake by organic aerosols, followed by heterogeneous oxidation, happens nearly at the collision frequency. Oxidation complicates the use of organic molecular markers such as hopanes for source apportionment, since receptor models assume markers are stable during transport.
Vikas Jaitak et al.
Natural product communications, 5(10), 1561-1566 (2010-12-03)
Phytochemical investigation of the aerial parts of Potentilla fulgens L. led to the isolation of two new triterpenes, potentene A (1) and potentene B (2). In addition, three known compounds afzelchin-4alpha --> 8"-catechin (3), epiafzelchin (4) and rutin (5) were
Ute Kraus et al.
Inhalation toxicology, 23(7), 431-447 (2011-06-07)
The aerosol components responsible for the adverse health effects of the exposure to particulate matter (PM) have not been conclusively identified, and there is especially little information on the role of particulate organic compounds (POC). This study evaluated the role
Geir Kildahl-Andersen et al.
Magnetic resonance in chemistry : MRC, 48(12), 951-954 (2010-10-01)
The full (1)H and (13)C NMR chemical shift assignment of 2α-methyl-17α(H),21β(H)-hopane is presented. This compound is formed in mature sediments from biogenic sources of 2β-methyl-17β(H),21β(H)-hopanoids, which include several cyanobacteria. In addition, full (1)H and (13)C NMR chemical shift data of
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商品

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.

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