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HCID 8166Erstellt: 23. Oktober 2026

Dodecanoyl chloride

DODECANOYL CHLORIDE · LACL · N-DODECANOYL CHLORIDE · Lauric chloride · LAUROYL CHLORIDE · Dodecanoyl chlorid · Lauroyl chloride,98% · LAURIC ACID CHLORIDE

https://huagongshe.com/de/chemical/8166

Molekülstruktur von Dodecanoyl chloride

Identifikatoren & physikalische Daten

CAS No.112-16-3
SummenformelC12H23ClO
Durchschnittliche Molmasse218,76 g/mol
Monoisotopische Masse218,143743 g/mol
SMILESCCCCCCCCCCCC(=O)Cl
InChIKeyNQGIJDNPUZEBRU-UHFFFAOYSA-N
PubChem CID8166
ChEMBLCHEMBL3561663
EC No.203-941-7
DTXSIDDTXSID5044368

Chemische & physikalische Eigenschaften

XLogP5,2
Polarare Oberfläche (TPSA)17,1
H-Brücken-Donoren0
H-Brücken-Akzeptoren1
Frei drehbare Bindungen10
Schwere Atome14
Formalladung0
Komplexität134
Color/FormWATER-WHITE LIQUID
LöslichkeitSOL IN ETHERSoluble in ethanol and methanol.reacts
Siedepunkt145 °C @ 18 MM HG134-137 °C/11 mmHg (lit.)
Schmelzpunkt-17 °C
BrechungsindexINDEX OF REFRACTION: 1.4458 @ 20 °C/Dn20/D 1.445
Physical DescriptionLiquidWater white liquid[HSDB] Colorless liquid[MSDSonline]
Other Experimental PropertiesDECOMP IN WATER, ALCOHOL
Dichte0.946 g/mL at 25 °C (lit.)
Dampfdruck0.5Pa at 20℃
Flammpunkt>230 °F
LagerbedingungenStore below +30°C.
AggregatzustandLiquid
FarbeClear
BRN1281201
StabilitätStable. Incompatible with strong oxidizing agents, amines, strong bases. Do not allow to come into contact with water or moisture.
InChI1S/C12H23ClO/c1-2-3-4-5-6-7-8-9-10-11-12(13)14/h2-11H2,1H3
InChIKeyNQGIJDNPUZEBRU-UHFFFAOYSA-N
SMILESCCCCCCCCCCCC(Cl)=O
CAS Datenbank112-16-3(CAS DataBase Reference)
NIST chemische InformationenDodecanoyl chloride(112-16-3)
EPA chemische InformationenDodecanoyl chloride (112-16-3)

Sicherheit & Vorschriften

GHS-EinstufungDangerH290 (17.2%): May be corrosive to metals [Warning Corrosive to Metals]H314 (99.5%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]H317 (56.5%): May cause an allergic skin reaction [Warning Sensitization, Skin]H318 (57%): Causes serious eye damage [Danger Serious eye damage/eye irritation]P234, P260, P261, P264, P264+P265, P272, P280, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P354+P338, P316, P317, P321, P333+P317, P362+P364, P363, P390, P405, P406, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 186 reports by companies from 12 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.
Regulatorische InformationenChemical: Dodecanoyl chlorideDodecanoyl chloride is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Dodecanoyl chloride are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)Status: Cease Manufacture Update: 07-10-2013 https://echa.europa.eu/registration-dossier/-/registered-dossier/1369Status: Active Update: 13-04-2021 https://echa.europa.eu/registration-dossier/-/registered-dossier/14344Lauroyl chloride: Does not have an individual approval but may be used under an appropriate group standard
Weitere SicherheitsinformationenIMAP assessments - Dodecanoyl chloride: Human health tier I assessmentIMAP assessments - Dodecanoyl chloride: Environment tier I assessment
GefahrenübersichtReacts violently with waterA corrosive substance that can cause injury to the skin, eyes, and respiratory tractInhalation may cause chemical pneumonitis[MSDSonline]
Hazard Classes and CategoriesMet. Corr. 1 (17.2%)Skin Corr. 1B (99.5%)Skin Sens. 1 (56.5%)Eye Dam. 1 (57%)
Unerwünschte WirkungenDermatotoxin - Skin burns.Toxic Pneumonitis - Inflammation of the lungs induced by inhalation of metal fumes or toxic gases and vapors.
Wassergefährdungsklasse (WGK)3
TSCA-Inventar-StatusTSCA listed
UN-TransportnummerUN 3265 8/PG 2
Zollcode29159080
R-Sätze (R)34-37-29-22-14
ToxizitätLD50 orally in Rabbit: 200 - 2000 mg/kg
GefahrensymboleC
Sicherheitshinweise (S)26-36/37/39-45-8
Gefahrenklasse8Skin Corr. 1B
VerpackungsgruppeII
Lagerklasse8A - Combustible corrosive hazardous materials
Gefahrstoffdaten112-16-3(Hazardous Substances Data)

Anwendungen & Verwendung

Verwenden

Lauroyl chloride is used as tailoring agent for chemical modification of nanocelluloses of different length, nanofibrillated cellulose and cellulose nanocrystals and in the preparation of acylated collagen with water solubility and better surface activity. It is also employed as organic low-friction boundary lubricant in the preparation of novel polyvinyl alcohol hydrogel.It is used in the synthesis of hemicellulose-based hydrophobic biomaterials.

Herstellung & Synthese

synthetische

Lauroyl chloride is synthesized by the reaction of lauric acid with thionyl chloride. Reaction: The flask was charged with lauric acid 1330 (200 g, 1.0 mol) and catalyst (imidazole, 2-methyl imidazole, 2.0 mol% based on the acid), and the mixture was heated with stirring to 90 C°. The stirred mixture was maintained at 90 C° for 1 h, at which time gaseous phosgene was introduced below the surface of the liquid at such a rate as to maintain a gentle phosgene reflux from the deflamator. Phosgene addition was regulated and calculated with the aid of a tubular flowmeter. The reaction was continued, generally within the temperature range 80–100 C°, until hydrogen chloride was no longer evolved (cessation of heat generation at the top of the water scrubber). The phosgene feed was stopped and the reaction mixture was kept at 85–95 C° with gentle phosgene reflux from the deflamator until the evolution of carbon dioxide had ceased (30–60 min, as evidenced by cessation of the gas entering at the base of the scrubber column). Occasionally, additional phosgene was required during this period to maintain phosgene reflux and to complete the reaction. Following complete reaction, the deflamator was replaced by a 10-in. (25 cm) glass helix packed distillation column fitted with a total reflux head, and dissolved phosgene was removed from the stirred reaction product by purging with dry nitrogen at 90 C° for 2 h. The product was distilled at 10 mmHg as a single fraction. Yield: 91–94.5% of lauroyl chloride.