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About This Item
Empirical Formula (Hill Notation):
C16H26O3
CAS Number:
Molecular Weight:
266.38
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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vapor density
9.2 (vs air)
vapor pressure
<1 mmHg ( 20 °C)
grade
technical
form
solid
bp
180-182 °C/5 mmHg (lit.)
mp
41-43 °C (lit.)
~45 °C
SMILES string
CCCCCCCCC\C=C/CC1CC(=O)OC1=O
InChI
1S/C16H26O3/c1-2-3-4-5-6-7-8-9-10-11-12-14-13-15(17)19-16(14)18/h10-11,14H,2-9,12-13H2,1H3/b11-10+
InChI key
UYCICMIUKYEYEU-ZHACJKMWSA-N
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General description
(2-Dodecen-1-yl)succinic anhydride is a carboxylic acid anhydride. It participates in the synthesis of alkenyl inulin derivatives and biosurfactants.
Application
(2-Dodecen-1-yl)succinic anhydride may be used in the following:
- Synthesis of amphiphilic N-[(2´-(dodec-2´-en-10-yl)succinoyl]chitosan.
- Chemical modification of sago starch, via esterification.
- Preparation of dodecenyl succinic anhydride (DDSA) gum arabic derivatives, via chemical modification of gum arabic.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
352.4 °F - closed cup
Flash Point(C)
178 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Application of hydrophobic ?-cyclodextrin polymer in separation of metal ions by plasticized membranes.
Kozlowski CA, et al.
Separation and Purification Technology, 46(3), 136-144 (2005)
The effect of anhydride modification of sago starch on the tensile and water absorption properties of sago-filled linear low-density polyethylene (LLDPE).
Abdul Khalil HPS, et al.
Polymer-Plastics Technology and Engineering, 40(3), 249-263 (2001)
Amphiphilic N-[2 (3)-(dodec-2'-en-1'-yl) succinoyl] chitosan: Synthesis and properties.
Tikhonov VE, et al.
Reactive functional Polymers, 68(2), 436-445 (2008)
Synthesis, characterization and emulsification properties of dodecenyl succinic anhydride derivatives of gum Arabic.
Wang H, et al.
Food Hydrocolloids, 37, 143-148 (2014)
S Kokubun et al.
Biomacromolecules, 14(8), 2830-2836 (2013-06-26)
Biosurfactants have been synthesized using a low energy, environmentally friendly process by the derivatization of inulin with octenyl (OSA) and dodecenyl (DDSA) succinic anhydrides in aqueous solution. The inulin and its derivatives have been characterized using gel permeation chromatography/multi angle
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