| Identification | More | [Name]
10-UNDECENOYL CHLORIDE | [CAS]
38460-95-6 | [Synonyms]
10-UNDECENOIC ACID CHLORIDE
10-UNDECENOYL CHLORIDE
10-UNDECYLENIC ACID CHLORIDE
10-UNDECYLENOYL CHLORIDE
DELTA 10 CIS-UNDECENOYL CHLORIDE
TIMTEC-BB SBB009003
UNDECENOYL CHLORIDE
UNDECYLENYL CHLORIDE
omega-Undecylenic acid chloride
omega-undecylenicacidchloride
Undecylenoyl chloride
undec-10-enoyl chloride
10-UNDECENOYL CHLORIDE DEST.
10-UNDECENOYL CHLORIDE 98+%
10-Nndecenoyl chloride, 98% | [EINECS(EC#)]
253-951-0 | [Molecular Formula]
C11H19ClO | [MDL Number]
MFCD00000772 | [Molecular Weight]
202.72 | [MOL File]
38460-95-6.mol |
| Chemical Properties | Back Directory | [Appearance]
clear yellow liquid | [Boiling point ]
120-122 °C10 mm Hg(lit.)
| [density ]
0.944 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.454(lit.)
| [Fp ]
200 °F
| [storage temp. ]
Store below +30°C. | [form ]
Liquid | [color ]
Clear yellow | [BRN ]
1635112 | [InChI]
InChI=1S/C11H19ClO/c1-2-3-4-5-6-7-8-9-10-11(12)13/h2H,1,3-10H2 | [InChIKey]
MZFGYVZYLMNXGL-UHFFFAOYSA-N | [SMILES]
C(Cl)(=O)CCCCCCCCC=C | [CAS DataBase Reference]
38460-95-6(CAS DataBase Reference) | [EPA Substance Registry System]
10-Undecenoyl chloride (38460-95-6) |
| Safety Data | Back Directory | [Hazard Codes ]
C | [Risk Statements ]
R34:Causes burns.
R37:Irritating to the respiratory system. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . | [RIDADR ]
UN 3265 8/PG 2
| [WGK Germany ]
3
| [RTECS ]
YQ2991000
| [TSCA ]
TSCA listed | [HazardClass ]
8 | [PackingGroup ]
III | [HS Code ]
29161910 | [Storage Class]
8A - Combustible corrosive hazardous materials | [Hazard Classifications]
Eye Dam. 1
Skin Corr. 1B
STOT SE 3 |
| Hazard Information | Back Directory | [Chemical Properties]
clear yellow liquid | [Uses]
10-Undecenoyl chloride was used as acylating reagent in the synthesis of cellulose ω-carboxyalkanoates and poly(ethylene glycol)–lipid amphiphiles. It was used in synthesis and modification of hyperbranched poly(glycidol). |
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