ChemicalBook >> CAS DataBase List >>11-DODECYN-1-OL

11-DODECYN-1-OL

CAS No.
18202-10-3
Chemical Name:
11-DODECYN-1-OL
Synonyms
Dodec-11-yn-1-ol;11-DODECYN-1-OL;11-dodecyn-1-01;odec-11-yn-1-ol;11-Dodecyne-1-ol
CBNumber:
CB3694686
Molecular Formula:
C12H22O
Molecular Weight:
182.3
MDL Number:
MFCD07780248
MOL File:
18202-10-3.mol
MSDS File:
SDS
Last updated:2026-05-28 04:30:23

11-DODECYN-1-OL Properties

Melting point 18.8°C (estimate)
Boiling point 285.73°C (rough estimate)
Density 0.8530 (estimate)
refractive index 1.4535 (estimate)
storage temp. 2-8°C
form <26°C Solid,>28°C Liquid
pka 15.20±0.10(Predicted)
color Colorless to off-white
InChI InChI=1S/C12H22O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h1,13H,3-12H2
InChIKey XNRAUTMOUDUPET-UHFFFAOYSA-N
SMILES C(O)CCCCCCCCCC#C

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P301+P312-P302+P352-P304+P340-P305+P351+P338

11-DODECYN-1-OL price More Price(25)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
ChemScene CS-W007273 11-Dodecyn-1-ol ≥97% 18202-10-3 5g $38 2026-06-04 Buy
ChemScene CS-W007273 11-Dodecyn-1-ol ≥97% 18202-10-3 10g $75 2026-06-04 Buy
ChemScene CS-W007273 11-Dodecyn-1-ol ≥97% 18202-10-3 25g $186 2026-06-04 Buy
ChemScene CS-W007273 11-Dodecyn-1-ol ≥97% 18202-10-3 100g $559 2026-06-04 Buy
Synthonix D56304 Dodec-11-yn-1-ol 98% 18202-10-3 250mg $43 2026-05-06 Buy
Product number Packaging Price Buy
CS-W007273 5g $38 Buy
CS-W007273 10g $75 Buy
CS-W007273 25g $186 Buy
CS-W007273 100g $559 Buy
D56304 250mg $43 Buy

11-DODECYN-1-OL Chemical Properties,Uses,Production

Uses

11-Dodecyn-1-ol is a synthetic intermediate of the sex pheromone (Z,E)-11,13,15-Hexadecatrienyl acetate for Thaumetopoea processionea[1].

Synthesis

NaH (7.5 g, 60% oil dispersion, 326 mmol) was added batchwise to a stirred 0 C solution of dodeca-3-yn-1-ol (10.0 g, 54.95 mmol; GF Smith) in ethylenediamine (40 mL).After 1 h, the temperature was raised to 70 C. The reaction mixture was cooled to 0 C for another 8 h and carefully terminated with ice-cold water (100 mL) and extracted with ether (3 x 60 mL). After another 8h, the reaction mixture was cooled to 0 C, carefully terminated with ice-cold water (100 mL) and extracted with ether (3 x 60 mL). The combined ether extracts were washed with water (100 mL). The aqueous washings were back-extracted with ether (3 x 60mL). The combined organic extracts were concentrated under vacuum and the residue was subjected to column chromatography using 10% EtOAc/hexane to obtain 11-dodecyne-1-ol (7.4 g, 74%) contaminated with 3-5% of other regioisomers (regioisomer).TLC: 30% EtOAc/hexane, Rf 0.4; 1H NMR (300 MHz, CDCl3). CDCl3) 3.66 (t, 2H, J = 7.3 Hz), 2.14-2.21 (m, 2H), 1.93 (t, J = 1.9 Hz, 1H), 1.20-1.63 (m, 16H).

References

[1] Gries R, et al. (Z, Z)-11, 13-Hexadecadienyl acetate and (Z, E)-11, 13, 15-hexadecatrienyl acetate: synergistic sex pheromone components of oak processionary moth, Thaumetopoea processionea (Lepidoptera: Thaumetopoeidae)[J]. Chemoecology, 2004, 14: 95-100...

11-DODECYN-1-OL Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 74)Suppliers
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Infinity SCI 400-106-2016 17800804092 admin@infsci.com China 471 55
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Shanghai YuanYe Biotechnology Co., Ltd. 15026964105 2881489226@qq.com China 89667 60

11-DODECYN-1-OL Spectrum

11-dodecyn-1-01 11-DODECYN-1-OL 11-Dodecyne-1-ol odec-11-yn-1-ol Dodec-11-yn-1-ol 18202-10-3