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Details

Stereochemistry ACHIRAL
Molecular Formula C12H25Br
Molecular Weight 249.231
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LAURYL BROMIDE

SMILES

CCCCCCCCCCCCBr

InChI

InChIKey=PBLNBZIONSLZBU-UHFFFAOYSA-N
InChI=1S/C12H25Br/c1-2-3-4-5-6-7-8-9-10-11-12-13/h2-12H2,1H3

HIDE SMILES / InChI

Molecular Formula C12H25Br
Molecular Weight 249.231
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Self-aggregation behavior of alkylated chitosan and its effect on the release of a hydrophobic drug.
2003
Enhanced cell volume regulation: a key protective mechanism of ischemic preconditioning in rabbit ventricular myocytes.
2003 Jan
Effects of CCCP-induced mitochondrial uncoupling and cyclosporin A on cell volume, cell injury and preconditioning protection of isolated rabbit cardiomyocytes.
2003 Jul
Synthesis and characterization of novel polyurethane cationomers with dipeptide sequences and alkylammonium groups.
2004
Catalysis by hydrophobically modified poly(propylenimine) dendrimers having quaternary ammonium and tertiary amine functionality.
2004 Sep 14
A study of oil droplet coalescence.
2007 Dec 1
Diverse self-assembly in soluble oligoazaacenes: a microscopy study.
2009 Aug 4
Synthesis of surfactants based on pentaerythritol. I. Cationic and zwitterionic gemini surfactants.
2009 Oct 16
Reaction of lithium diethylamide with an alkyl bromide and alkyl benzenesulfonate: origins of alkylation, elimination, and sulfonation.
2010 Dec 17
A molecular mechanism for eflornithine resistance in African trypanosomes.
2010 Nov 24
3-(12-Bromo-dodec-yl)-1,5-dimethyl-1H-1,5-benzodiazepine-2,4(3H,5H)-dione.
2010 Oct 13
Assessment of heterologous butyrate and butanol pathway activity by measurement of intracellular pathway intermediates in recombinant Escherichia coli.
2010 Sep
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:55:06 GMT 2023
Edited
by admin
on Fri Dec 15 17:55:06 GMT 2023
Record UNII
90T93TX09D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LAURYL BROMIDE
MI  
Systematic Name English
DODECYL BROMIDE
Systematic Name English
NSC-6786
Code English
LAURYL BROMIDE [MI]
Common Name English
1-BROMODODECANE
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
205-587-9
Created by admin on Fri Dec 15 17:55:06 GMT 2023 , Edited by admin on Fri Dec 15 17:55:06 GMT 2023
PRIMARY
MESH
C073960
Created by admin on Fri Dec 15 17:55:06 GMT 2023 , Edited by admin on Fri Dec 15 17:55:06 GMT 2023
PRIMARY
NSC
6786
Created by admin on Fri Dec 15 17:55:06 GMT 2023 , Edited by admin on Fri Dec 15 17:55:06 GMT 2023
PRIMARY
PUBCHEM
8919
Created by admin on Fri Dec 15 17:55:06 GMT 2023 , Edited by admin on Fri Dec 15 17:55:06 GMT 2023
PRIMARY
MERCK INDEX
m6714
Created by admin on Fri Dec 15 17:55:06 GMT 2023 , Edited by admin on Fri Dec 15 17:55:06 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID2044395
Created by admin on Fri Dec 15 17:55:06 GMT 2023 , Edited by admin on Fri Dec 15 17:55:06 GMT 2023
PRIMARY
CAS
143-15-7
Created by admin on Fri Dec 15 17:55:06 GMT 2023 , Edited by admin on Fri Dec 15 17:55:06 GMT 2023
PRIMARY
WIKIPEDIA
1-Bromododecane
Created by admin on Fri Dec 15 17:55:06 GMT 2023 , Edited by admin on Fri Dec 15 17:55:06 GMT 2023
PRIMARY
FDA UNII
90T93TX09D
Created by admin on Fri Dec 15 17:55:06 GMT 2023 , Edited by admin on Fri Dec 15 17:55:06 GMT 2023
PRIMARY