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13849-96-2

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13849-96-2 Usage

Triterpenoid compound

17ALPHA(H),21ALPHA(H)-HOPANE is a natural compound that belongs to the triterpenoid class, which are a group of organic compounds derived from the isoprene unit.

Found in petroleum and sedimentary rocks

This compound is commonly found in petroleum and sedimentary rocks, making it a useful biomarker for identifying the source of petroleum.

C30 compound

17ALPHA(H),21ALPHA(H)-HOPANE has a molecular formula of C30H50, indicating that it is composed of 30 carbon atoms and 50 hydrogen atoms.

Tetracyclic structure

The compound has a complex structure consisting of four fused rings, which gives it its unique properties.

Biomarker for petroleum source rocks

17ALPHA(H),21ALPHA(H)-HOPANE is used as a biomarker to identify the source of petroleum, as its presence indicates the presence of ancient photosynthetic organisms.

Molecular marker

The compound is also used as a molecular marker for the presence of ancient photosynthetic organisms, which can provide information about the age and origin of the petroleum.

Paleoclimate and paleoenvironmental studies

17ALPHA(H),21ALPHA(H)-HOPANE is used as a proxy for organic matter and temperature conditions in ancient sedimentary environments, which can provide insights into past climate and environmental conditions.

Tracing oil migration

The compound can be used to trace the movement of oil through geological formations, which can help in locating and extracting petroleum resources.

Assessing maturity of petroleum source rocks

The presence and concentration of 17ALPHA(H),21ALPHA(H)-HOPANE in source rocks can provide information about the maturity of the rocks and the potential for petroleum generation.

Check Digit Verification of cas no

The CAS Registry Mumber 13849-96-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,4 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13849-96:
(7*1)+(6*3)+(5*8)+(4*4)+(3*9)+(2*9)+(1*6)=132
132 % 10 = 2
So 13849-96-2 is a valid CAS Registry Number.
InChI:InChI=1/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

13849-96-2 Well-known Company Product Price

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  • Sigma-Aldrich

  • (90656)  17α(H),21β(H)-Hopanesolution  0.1 mg/mL in isooctane, analytical standard

  • 13849-96-2

  • 90656-1ML

  • 20,334.60CNY

  • Detail

13849-96-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 17ALPHA(H),21ALPHA(H)-HOPANE

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13849-96-2 SDS

13849-96-2Relevant articles and documents

Heating of hop-17(21)-ene in molten sulphur: A route to new sedimentary biomarkers of the hopane series?

Bisseret,Rohmer

, p. 5295 - 5298 (1993)

On heating in liquid sulphur, the unsaturated hopanoid hop-17(21)-ene 1 was converted to a major extent into the series of organo-sulphur products 5-9, all of interest as potential sedimentary biomarkers.

Concise syntheses of bacteriohopanetetrol and its glucosamine derivative

Pan, Weidong,Zhang, Yongmin,Liang, Guangyi,Vincent, Stephane P.,Sinay, Pierre

, p. 3445 - 3447 (2007/10/03)

This study describes the syntheses of bacteriohopanetetrol and its glucosamine derivative through a key direct coupling of a ribose derivative to the hopane skeleton. The Royal Society of Chemistry 2005.

Neriifoliol: A new pentacyclic triterpene alcohol from Oleandra neriifolia

Pandey,Mitra

, p. 1353 - 1357 (2007/10/14)

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