U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C6H19NSi2
Molecular Weight 161.3928
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HEXAMETHYLDISILAZANE

SMILES

C[Si](C)(C)N[Si](C)(C)C

InChI

InChIKey=FFUAGWLWBBFQJT-UHFFFAOYSA-N
InChI=1S/C6H19NSi2/c1-8(2,3)7-9(4,5)6/h7H,1-6H3

HIDE SMILES / InChI

Molecular Formula C6H19NSi2
Molecular Weight 161.3928
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Bone is not essential for osteoclast activation.
2010-09-17
Difluorobenzocyclooctyne: synthesis, reactivity, and stabilization by beta-cyclodextrin.
2010-08-25
The pneumococcal serine-rich repeat protein is an intra-species bacterial adhesin that promotes bacterial aggregation in vivo and in biofilms.
2010-08-12
[Fe(4)S(4)](q) cubane clusters (q = 4+, 3+, 2+) with terminal amide ligands.
2010-07-19
Synthesis and antiprotozoal activity of 2,5-bis[amidinoaryl]thiazoles.
2010-05-15
Bis(N-triisopropyl-silyl-quinolin-8-aminato)nickel(II).
2009-12-04
Solid-state (49/47)Ti NMR of titanium-based MCM-41 hybrid materials.
2009-11-03
Reversible transformation of a stable monomeric silicon(II) compound into a stable disilene by phase transfer: experimental and theoretical studies of the system {[(Me3Si)2N](Me5C5)Si}n with n = 1,2.
2009-09-02
Synthesis, structure, and reactivity of low-coordinate 1,1,3,3-tetraethylguanidinate complexes.
2009-08-17
Newly characterised ex vivo colospheres as a three-dimensional colon cancer cell model of tumour aggressiveness.
2009-08-04
pH-responsive biodegradable micelles based on acid-labile polycarbonate hydrophobe: synthesis and triggered drug release.
2009-07-13
Beta-diketiminato calcium and magnesium amides; model complexes for hydroamination catalysis.
2009-05-18
Hydrofluoric-acid-resistant and hydrophobic pure-silica-zeolite MEL low-dielectric-constant films.
2009-05-05
Synthesis and characterization of group 11 1,1,3,3-tetraalkylguanidinate (TAG) clusters: [M2(mu-TAG){mu-N(SiMe3)2}]2 (M = Cu, Ag, and Au).
2009-03-16
Synthesis of an imprinted hybrid organic-inorganic polymeric sol-gel matrix toward the specific binding and isotherm kinetics investigation of creatinine.
2009-03-15
[μ-Bis(trimethyl-silyl)amido]bis-[μ-N,N-dimethyl-N',N''-bis-(trimethyl-silyl)guanidinato]-triangulo-tricopper(I).
2009-03-14
Synthesis and characterization of lithium hemiporphyrazines.
2009-02-16
Solution interaction of potassium and calcium bis(trimethylsilyl)amides; preparation of Ca[N(SiMe3)2]2 from dibenzylcalcium.
2009-02-16
An Ugi reaction in the total synthesis of (-)-dysibetaine.
2009
Mercury or silver atoms bridging trinuclear titanium imido-nitrido systems.
2008-12-28
Sequential and selective Buchwald-Hartwig amination reactions for the controlled functionalization of 6-bromo-2-chloroquinoline: synthesis of ligands for the Tec Src homology 3 domain.
2008-11-21
Silica passivation efficiency monitored by a surface-bound fluorescent dye.
2008-08-19
Displayed correlation between gene expression profiles and submicroscopic alterations in response to cetuximab, gefitinib and EGF in human colon cancer cell lines.
2008-08-08
Ammonium benzene-phospho-nate.
2008-07-26
Surface property and in vitro biodegradation of microspheres fabricated by poly(epsilon-caprolactone-b-ethylene oxide) diblock copolymers.
2008-03-15
Reversibility in the protonolysis of a beta-diketiminate stabilised calcium bis(trimethylsilyl)amide with benzylamine.
2008-03-14
Quantification of cell edge velocities and traction forces reveals distinct motility modules during cell spreading.
2008
Zinc complexes of the biomimetic N,N,O ligand family of substituted 3,3-bis(1-alkylimidazol-2-yl)propionates: the formation of oxalate from pyruvate.
2007-11
Structure and reaction mechanism of basil eugenol synthase.
2007-10-03
A stable chiral diaminocyclopropenylidene.
2007-09-21
FeSO4 x 7H2O-catalyzed four-component synthesis of protected homoallylic amines.
2007-07-06
Efficient nucleophilic aromatic substitution between aryl nitrofluorides and alkynes.
2007-07-05
Synthesis and structural characterisation of lithium and sodium 2,6-dibenzylphenolate complexes.
2006-07-21
1,2-Eliminations in a novel reductive coupling of nitroarenes to give azoxy arenes by sodium bis(trimethylsilyl)amide.
2005-07-21
Base-promoted acyloin rearrangement of 1,8-di-tert-butyldimethylsilyloxybicyclo[2.2.2]oct-5-en-2-ones.
2005-06
C-H Activation (gamma-deprotonation) of a Sm(III) bis(trimethylsilyl)amide complex via macrocyclic stabilisation of the sodium counter ion.
2005-03-28
Unprecedented catalytic asymmetric reduction of N-H imines.
2005-01-20
The (Me5C5)Si+ cation: a stable derivative of HSi+.
2004-08-06
Determination of the absolute structure of (+)-cystothiazole B.
2004-06
Silylation reaction of dextran: effect of experimental conditions on silylation yield, regioselectivity, and chemical stability of silylated dextrans.
2003-09-10
Linear and cyclic polysilanes containing the bis(trimethylsilyl)amino group: synthesis, reactions, and spectroscopic characterization.
2003-07-28
Synthesis of 11C-amides using [11C]carbon monoxide and in situ activated amines by palladium-mediated carboxaminations.
2003-02-07
Structural studies of N,N'-di(ortho-fluorophenyl)formamidine group 1 metallation.
2003-01-20
Analogues of thiolactomycin: potential drugs with enhanced anti-mycobacterial activity.
2002-10
Synthesis and characterization of endcapped C18 stationary phases using a silica hydride intermediate.
2002-02-22
Palladium-catalyzed synthesis of arylamines from aryl halides and lithium bis(trimethylsilyl)amide as an ammonia equivalent.
2001-08-23
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:12:33 GMT 2025
Edited
by admin
on Mon Mar 31 19:12:33 GMT 2025
Record UNII
H36C68P1BH
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-93895
Preferred Name English
HEXAMETHYLDISILAZANE
HSDB   MI  
Systematic Name English
HEXAMETHYLDISILAZANE [MI]
Common Name English
HMDS
Common Name English
1,1,1-TRIMETHYL-N-(TRIMETHYLSILYL)SILANAMINE
Systematic Name English
HEXAMETHYLDISILAZANE [HSDB]
Common Name English
Code System Code Type Description
SMS_ID
100000170857
Created by admin on Mon Mar 31 19:12:33 GMT 2025 , Edited by admin on Mon Mar 31 19:12:33 GMT 2025
PRIMARY
ECHA (EC/EINECS)
213-668-5
Created by admin on Mon Mar 31 19:12:33 GMT 2025 , Edited by admin on Mon Mar 31 19:12:33 GMT 2025
PRIMARY
CAS
999-97-3
Created by admin on Mon Mar 31 19:12:33 GMT 2025 , Edited by admin on Mon Mar 31 19:12:33 GMT 2025
PRIMARY
NSC
93895
Created by admin on Mon Mar 31 19:12:33 GMT 2025 , Edited by admin on Mon Mar 31 19:12:33 GMT 2025
PRIMARY
CHEBI
85068
Created by admin on Mon Mar 31 19:12:33 GMT 2025 , Edited by admin on Mon Mar 31 19:12:33 GMT 2025
PRIMARY
DAILYMED
H36C68P1BH
Created by admin on Mon Mar 31 19:12:33 GMT 2025 , Edited by admin on Mon Mar 31 19:12:33 GMT 2025
PRIMARY
EVMPD
SUB185133
Created by admin on Mon Mar 31 19:12:33 GMT 2025 , Edited by admin on Mon Mar 31 19:12:33 GMT 2025
PRIMARY
RXCUI
1986434
Created by admin on Mon Mar 31 19:12:33 GMT 2025 , Edited by admin on Mon Mar 31 19:12:33 GMT 2025
PRIMARY
EPA CompTox
DTXSID2025395
Created by admin on Mon Mar 31 19:12:33 GMT 2025 , Edited by admin on Mon Mar 31 19:12:33 GMT 2025
PRIMARY
MESH
C024548
Created by admin on Mon Mar 31 19:12:33 GMT 2025 , Edited by admin on Mon Mar 31 19:12:33 GMT 2025
PRIMARY
WIKIPEDIA
Bis(trimethylsilyl)amine
Created by admin on Mon Mar 31 19:12:33 GMT 2025 , Edited by admin on Mon Mar 31 19:12:33 GMT 2025
PRIMARY
PUBCHEM
13838
Created by admin on Mon Mar 31 19:12:33 GMT 2025 , Edited by admin on Mon Mar 31 19:12:33 GMT 2025
PRIMARY
FDA UNII
H36C68P1BH
Created by admin on Mon Mar 31 19:12:33 GMT 2025 , Edited by admin on Mon Mar 31 19:12:33 GMT 2025
PRIMARY
HSDB
7226
Created by admin on Mon Mar 31 19:12:33 GMT 2025 , Edited by admin on Mon Mar 31 19:12:33 GMT 2025
PRIMARY
MERCK INDEX
m5995
Created by admin on Mon Mar 31 19:12:33 GMT 2025 , Edited by admin on Mon Mar 31 19:12:33 GMT 2025
PRIMARY Merck Index