3,5,5-Trimethylhexanoyl chloride

Suppliers

Names

[ Name ]:
3,5,5-Trimethylhexanoyl chloride

[Synonym ]:
Isononanoic acid chloride
EINECS 253-168-4
3,5,5-trimethyl hexanoic acid chloride
3,5,5-TriMethylhexanoyl Chloride
3,5,5-Trimethyl-hexanoylchlorid
3,5,5-trimethyl hexanoyl chloride
Hexanoyl chloride,3,5,5-trimethyl
Isononanoyl chloride
MFCD00044028
3,5,5-trimethyl-1-hexanoyl chloride

Chemical & Physical Properties

[ Density]:
0.93 g/mL at 25 °C(lit.)

[ Boiling Point ]:
188-190 °C(lit.)

[ Melting Point ]:
188-190ºC

[ Molecular Formula ]:
C₉H₁₇ClO

[ Molecular Weight ]:
176.68400

[ Flash Point ]:
284 °F

[ Exact Mass ]:
176.09700

[ PSA ]:
17.07000

[ LogP ]:
3.21420

[ Index of Refraction ]:
n20/D 1.436(lit.)

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS05, GHS06

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H290-H302-H314-H317-H330-H412

[ Supplemental HS ]:
Reacts violently with water.

[ Precautionary Statements ]:
P260-P273-P280-P284-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
C:Corrosive;

[ Risk Phrases ]:
R14;R20;R34

[ Safety Phrases ]:
S26-S27-S36/37/39-S45

[ RIDADR ]:
3389

[ WGK Germany ]:
1

[ RTECS ]:
MP4560000

[ Packaging Group ]:
III

[ Hazard Class ]:
8

[ HS Code ]:
2915900090

Precursor & DownStream

Precursor

3,5,5-Trimethylhexanal
3,5,5-Trimethylhexanoic acid
UNII:O5KUD6I57K

DownStream

3,5,5-Trimethylhexanoyl peroxide
ethyl 3,5,5-trimethyl hexanoate

Customs

[ HS Code ]: 2915900090

[ Summary ]:
2915900090 other saturated acyclic monocarboxylic acids and their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) MFN tariff:5.5% General tariff:30.0%

Articles

Antibacterial barbituric acid analogues inspired from natural 3-acyltetramic acids; synthesis, tautomerism and structure and physicochemical property-antibacterial activity relationships.

Molecules 20(3) , 3582-627, (2015)

The synthesis, tautomerism and antibacterial activity of novel barbiturates is reported. In particular, 3-acyl and 3-carboxamidobarbiturates exhibited antibacterial activity, against susceptible and s...

Chemical synthesis, isolation and characterization of a-N-fattyacyl colistin nonapeptide with special reference to the correlation between antimicrobial activity and carbon number of fattyacyl moiety. Chihara S, et al.

Agric. Biol. Chem. 38(3) , 521-529, (1974)

Outer-Sphere Coordination Chemistry: Amido-Ammonium Ligands as Highly Selective Tetrachloridozinc (II) ate Extractants. Turkington JR, et al.

Inorg. Chem. 51(23) , 12805-12819, (2012)

(3,5,5-TRIMETHYLHEXANOYL)-FERROCENE
3,5,5-Trimethylhexanoyl peroxide
dibutylbis[(3,5,5-trimethylhexanoyl)oxy]stannane
2-(3,5,5-TRIMETHYLHEXANOYL)OXAZOLE
3-(5,5-dimethylpyrrolidin-1-ium-2-yl)-1H-indole,chloride
3-(5,5-dimethyl-3-octadecyl-1,3-thiazolidin-2-yl)-4-hydroxybenzenesulfonyl chloride
Ethyl (3S)-10-(4-amino-1-piperazinyl)-9-fluoro-2,3-dihydro-3-methyl-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylate
7,10,11,12-Tetrahydro-7-(2-hydroxyphenyl)-10,10-dimethylbenz[c]acridin-8(9H)-one
4-[2-(Cyclopropanecarbonyl-amino)-[1,2,4]triazolo[1,5-a]pyridin-5-yl]-benzoic acid
6-Bromo-2-pyridin-2-ylquinoline-4-carbonyl chloride hydrochloride
1-(Pyrazin-2-yl)propan-2-amine trihydrochloride
Sodium 2-methanesulfonamido-3-methylbutanoate
tert-butyl N-(2-aminocycloheptyl)carbamate
3-(2,4-Dimethoxyphenyl)-3-oxopropanal
N-hexylpiperidine-2-carboxamide
2-[[[4-(Methylthio)phenyl]methyl]thio]acetic acid

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.