ContaminantDB: 6-(3-aminopropyl)-2,2,4,4,6,8,8,10,10-nonamethyl-3,5,7,9-tetraoxa-2,4,6,8,10-pentasilaundecane

Identification Taxonomy Biological Properties Physical Properties Toxicity Profile Spectra Concentrations Links References XML

Record Information

Version

1.0

Creation Date

2016-06-03 11:53:31 UTC

Update Date

2016-11-09 01:23:05 UTC

Accession Number

CHEM044220

Identification

Common Name

6-(3-aminopropyl)-2,2,4,4,6,8,8,10,10-nonamethyl-3,5,7,9-tetraoxa-2,4,6,8,10-pentasilaundecane

Class

Small Molecule

Description

Not Available

Contaminant Sources

STOFF IDENT Compounds

Contaminant Type

Not Available

Chemical Structure

MOL SDF PDB SMILES InChI

Synonyms

Not Available

Chemical Formula

C₁₄H₄₁NO₄Si₅

Average Molecular Mass

427.910 g/mol

Monoisotopic Mass

427.188 g/mol

CAS Registry Number

99363-37-8

IUPAC Name

6-(3-aminopropyl)-2,2,4,4,6,8,8,10,10-nonamethyl-3,5,7,9-tetraoxa-2,4,6,8,10-pentasilaundecane

Traditional Name

6-(3-aminopropyl)-2,2,4,4,6,8,8,10,10-nonamethyl-3,5,7,9-tetraoxa-2,4,6,8,10-pentasilaundecane

SMILES

C[Si](C)(C)O[Si](C)(C)O[Si](C)(CCCN)O[Si](C)(C)O[Si](C)(C)C

InChI Identifier

InChI=1S/C14H41NO4Si5/c1-20(2,3)16-22(7,8)18-24(11,14-12-13-15)19-23(9,10)17-21(4,5)6/h12-15H2,1-11H3

InChI Key

PXUXLBITYUZGOV-UHFFFAOYSA-N

Chemical Taxonomy

Description

belongs to the class of organic compounds known as siloxanes. These are saturated silicon-oxygen hydrides with unbranched or branched chains of alternating silicon and oxygen atoms (each silicon atom is separated from its nearest silicon neighbours by single oxygen atoms). The general structure of unbranched siloxanes is H3Si[OSiH2]nOSiH3. H3Si[OSiH2]nOSiH[OSiH2OSiH3]2 is an example of a branched siloxane. By extension hydrocarbyl derivatives are commonly included.

Kingdom

Organic compounds

Super Class

Organometallic compounds

Class

Organometalloid compounds

Sub Class

Organosilicon compounds

Direct Parent

Siloxanes

Alternative Parents

Substituents

Siloxane
Trialkylheterosilane
Organoheterosilane
Organic metalloid salt
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Organic salt
Primary amine
Organonitrogen compound
Primary aliphatic amine
Amine
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Biological Properties

Status

Detected and Not Quantified

Origin

Not Available

Cellular Locations

Not Available

Biofluid Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Applications

Not Available

Biological Roles

Not Available

Chemical Roles

Not Available

Physical Properties

State

Not Available

Appearance

Not Available

Experimental Properties

Property	Value
Melting Point	Not Available
Boiling Point	Not Available
Solubility	Not Available

Predicted Properties

Property	Value	Source
Water Solubility	0.00073 g/L	ALOGPS
logP	4.77	ALOGPS
logP	2.93	ChemAxon
logS	-5.8	ALOGPS
pKa (Strongest Basic)	10.21	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	62.94 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	88.49 m³·mol⁻¹	ChemAxon
Polarizability	44.46 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	1	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-01t9-0000900000-3a37bd52b9f58d755985	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-03dm-8921200000-e451ae70b15338224757	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-022l-8249100000-3993027f3222dfe1da19	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-0i00-0109500000-0fb118de71dbd91f2515	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-000b-9742000000-60e9819226fd0b4c55c1	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-0a4j-9211000000-8681288c04d5b01d5a97	Spectrum

Toxicity Profile

Route of Exposure

Not Available

Mechanism of Toxicity

Not Available

Metabolism

Not Available

Toxicity Values

Not Available

Lethal Dose

Not Available

Carcinogenicity (IARC Classification)

Not Available

Uses/Sources

Not Available

Minimum Risk Level

Not Available

Health Effects

Not Available

Symptoms

Not Available

Treatment

Not Available

Concentrations

Not Available

External Links

DrugBank ID

Not Available

HMDB ID

Not Available

FooDB ID

Not Available

Phenol Explorer ID

Not Available

KNApSAcK ID

Not Available

BiGG ID

Not Available

BioCyc ID

Not Available

METLIN ID

Not Available

PDB ID

Not Available

Wikipedia Link

Not Available

Chemspider ID

Not Available

ChEBI ID

Not Available

PubChem Compound ID

23560364

Kegg Compound ID

Not Available

YMDB ID

Not Available

ECMDB ID

Not Available

References

Synthesis Reference

Not Available

MSDS

Not Available

General References

Not Available

6-(3-aminopropyl)-2,2,4,4,6,8,8,10,10-nonamethyl-3,5,7,9-tetraoxa-2,4,6,8,10-pentasilaundecane (CHEM044220)

Structure for CHEM044220: 6-(3-aminopropyl)-2,2,4,4,6,8,8,10,10-nonamethyl-3,5,7,9-tetraoxa-2,4,6,8,10-pentasilaundecane