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Merck
CN

90656

Supelco

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
EC 号:
208-759-1
MDL编号:
MFCD16660343
UNSPSC代码:
85151701
PubChem化学物质编号:
329769939
NACRES:
NA.24

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等级

analytical standard

质量水平

100

保质期

limited shelf life, expiry date on the label

浓度

0.1 mg/mL in isooctane

技术

HPLC: suitable
gas chromatography (GC): suitable

应用

food and beverages

包装形式

single component solution

储存温度

−20°C

SMILES字符串

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

相关类别

应用

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

警示用语：

Danger

危险分类

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

靶器官

Central nervous system

储存分类代码

3 - Flammable liquids

WGK

WGK 2

闪点(°F)

10.4 °F - closed cup

闪点(°C)

-12 °C - closed cup

个人防护装备

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

法规信息

危险化学品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCN2543
BCCM7183
BCCJ7098
BCCF3737
BCCB4929

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Chintalapati Venkata Ramana et al.
Antonie van Leeuwenhoek, 103(4), 885-898 (2013-01-12)
Strain JC90(T) was isolated from a soda lake in Lonar, India. Strain JC90(T) maintains its external pH to 8.5 and participates in halite formation. Based on 16S rRNA gene sequence similarity studies, strain JC90(T) was found to belong to the
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
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.
P V Welander et al.
Geobiology, 10(2), 163-177 (2012-01-10)
Hopanes preserved in both modern and ancient sediments are recognized as the molecular fossils of bacteriohopanepolyols, pentacyclic hopanoid lipids. Based on the phylogenetic distribution of hopanoid production by extant bacteria, hopanes have been used as indicators of specific bacterial groups
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
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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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