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13-??????,

13-??????,
13-??????, ??? ???
?? ??:
112-84-5
???:
13-??????,
???(??):
??????;13-???????,;13-??????,;13-???????,(Z);??????;(Z)-13-???????;(Z)-???-13-?????;13-???????, (13Z)-;13-???????, (Z)-;??-13-???????;??-13-????????;??? ????;??? ????;?????;???? ????;??? ????-?????
???:
Erucamide
???(??):
ERUCAMIDE;13-DOCOSENAMIDE;ERUCYLAMIDE;13Z-DOCOSENAMIDE;(z)-13-docosenamide;(Z)-docos-13-enamide;ERUCIC AMIDE;CIS-13-DOCOSENOAMIDE;Erucic acid amide;CIS-13-DOCOSENAMIDE
CBNumber:
CB0136080
???:
C22H43NO
??? ??:
337.58
MOL ??:
112-84-5.mol
MSDS ??:
SDS

13-??????, ??

???
75-85 °C 79-81 °C (lit.)
?? ?
473.86°C (rough estimate)
??
0.9417 (rough estimate)
???
0-0Pa at 25℃
???
1.5614 (estimate)
???
230 °C
?? ??
-20°C
???
DMSO(?? 40mg/ml) ?? ?(?? ? ?? 25mg/ml)? ?????.
??? ??
??
??? ??
??? ??
?? ?? (pKa)
16.61±0.40(Predicted)
??
???
???
????? ???
Henry's Law Constant
3.5×100 mol/(m3Pa) at 25℃, HSDB (2015)
???
????. ?? ???? ???? ????.
??? ?? ??
?? ??
????
InChI
1S/C22H43NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22(23)24/h9-10H,2-8,11-21H2,1H3,(H2,23,24)/b10-9-
InChIKey
UAUDZVJPLUQNMU-KTKRTIGZSA-N
SMILES
[H]\C(CCCCCCCC)=C(/[H])CCCCCCCCCCCC(N)=O
LogP
8
CAS ??????
112-84-5(CAS DataBase Reference)
NIST
13-Docosenamide, (z)-(112-84-5)
EPA
13-Docosenamide, (13Z)- (112-84-5)
??
  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
??? ?? Xi
?? ???? ?? 36/37/38
????? 26-36-37/39
WGK ?? 1
TSCA TSCA listed
HS ?? 29241990
???? ??? 11 - Combustible Solids
?? ?? ??? 112-84-5(Hazardous Substances Data)
???? ?? KE-12791
????(GHS): Exclamation Mark (GHS07)
?? ?: Warning
??·?? ??:
?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
H315 ??? ??? ??? ????? ?? ????? ?? 2 ?? P264, P280, P302+P352, P321,P332+P313, P362
H319 ?? ?? ??? ??? ?? ? ?? ?? ??? ?? ?? 2A ?? P264, P280, P305+P351+P338,P337+P313P
H335 ?? ???? ??? ? ?? ?? ???? ?? - 1? ??;???? ?? ?? 3 ??
??????:
P261 ??·?·??·???·??·...·????? ??? ????.
P305+P351+P338 ?? ??? ? ?? ?? ???? ????. ???? ?????? ?????. ?? ????.
NFPA 704
0
2 0

13-??????, MSDS


cis-13-Docosenoamide

13-??????, C??? ??, ??, ??

??

Erucamide is also known as 13-Docosenamide or Erucylamide. It is in the form of white flakes or beads. It is soluble in isopropanol, slightly soluble in alcohol and acetone.1 In industry, cis-13-docosenoamide is used in the formulations of anti-adhesive agents, lubricants, and lubricant additives to reduce their friction coefficient and to make films easier to handle.2 It is used as a standard to determine fatty acid amides in polyethylene packaging film by GC/MS.3

??? ??

Erucamide is a fatty acid amide derived from erucic acid, which is found in vegetable oil. It is a odorless waxy solid that can dissolve in isopropanol and has low solubility in alcohol and acetone. It is also combustible. Its molecular structure consists of a long unsaturated C22 chain and a polar amine group, which gives it strong surface polarity, a high melting point, and good thermal stability. Because of these properties, it finds extensive applications in industries such as plastics, rubber, printing, and machinery.

??

Erucamide is primarily used as a polymer additive, with plastic additive 21 is a plasticizer; used in preparation of natural mineral modified degradable polymer flame-retardant composite material.

?? ??

Erucamide is prepared by reaction of erucic acid with anhydrous ammonia. The reaction of erucic acid with anhydrous ammonia is as follows: C22H42O2 + NH3 → C22H43NO2.

?? ??

Erucamide is a migratory additive that is commonly placed in polyolefin films to reduce their coefficient of friction (COF), a good attribute for high speed packaging operations.

???? ??

13-Docosenamide is the amide of docosenoic acid. It was first identified in the cerebrospinal fluid of sleep-deprived cats. It has also been detected in the cerebrospinal fluid of rats and humans. 13-Docosenamide causes reduced mobility and slightly lessened awareness in rats, whereas 9-octadecenamide induces physiological sleep.

?? ??

[1] MIAO-MIAO LI . Antidepressant and anxiolytic-like behavioral effects of erucamide, a bioactive fatty acid amide, involving the hypothalamus–pituitary–adrenal axis in mice[J]. Neuroscience Letters, 2017, 640: Pages 6-12. DOI:10.1016/j.neulet.2016.12.072.
[2] LIEROP B V, CASTLE L, FEIGENBAUM A, et al. Spectra for the Identification of Additives in Food Packaging[C]. 1998: 0. DOI:10.1007/978-94-011-5222-8.
[3] https://pubchem.ncbi.nlm.nih.gov/compound/Erucylamide#section=Use-and-Manufacturing
[4] https://www.sigmaaldrich.com/catalog/product/aldrich/280577lang=de&region=DE
[5] I. QUIJADA-GARRIDO. Desorption of Erucamide Vapor in Vacuum from Erucamide/Isotactic Polypropylene Films 1[J]. Macromolecules, 1996, 29 27: 8791-8797. DOI:10.1021/ma961065i.

13-??????, ?? ?? ? ???

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?? ??


13-??????, ?? ??

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??? ?? ??? ?? ?? ? ??
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13-??????, ?? ??:

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