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Suppliers for CAS
5986-55-0
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Properties | | CAS |
5986-55-0 | | Formula |
C15H26O | | EINECS |
227-807-2 |
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8 Registered suppliers
Dayang Chem (Hangzhou) Co.,Ltd.
P.R.China
Leap Chem Co., Ltd
P.R.China
Molecular Formula: C15H26O Molecular Weight: 222.37 HS Code: 29061990
More details are to be found here
Van Aroma
Indonesia
Finetech Industry Limited
P.R.China
More details are to be found here
BOC Sciences
USA
Description : Patchouli alcohol, coming from the herbs of Pogostemon cablin (Blanco) Benth, has the potential to treat inflammation as well as bacterial and fungal infections. It exhibited selective antibacterial activity against Helicobacter pylori, without influencing the major normal gastrointestinal bacteria. Patchouli alcohol significantly accelerated the recovery of the UV-induced skin lesions, evidently through anti-oxidant and anti-inflammatory action, as well as down-regulation of the MMP-1 and MMP-3 expression. - Molecular Weight :222.36
- Purity :> 98%
Molecular Formula : C15H26O Canonical SMILES : CC1CCC2(C(C3CCC2(C1C3)C)(C)C)O InChI : InChI=1S/C15H26O/c1-10-5-8-15(16)13(2,3)11-6-7-14(15,4)12(10)9-11/h10-12,16H,5-9H2,1-4H3/t10-,11+,12-,14-,15+/m0/s1
InChIKey :
GGHMUJBZYLPWFD-CUZKYEQNSA-N
Appearance :
Powder
Application :
Antibacterial/anti-inflammatory
Synonyms :
1,6-Methanonaphthalen-1(2H)-ol, octahydro-4,8a,9,9-tetramethyl-, (1alpha,4beta,4aalpha,6beta,8aalpha)-; 1,6-Methanonaphthalen-1(2H)-ol, octahydro-4,8a,9,9-tetramethyl-, [1R-(1alpha,4beta,4aalpha,6beta,8aalpha)]-; Patchoulol; patchouli camphor; patchoulanol
More details are to be found here
Chemos GmbH & Co. KG
Germany
Description : Patchouli alcohol, coming from the herbs of Pogostemon cablin (Blanco) Benth, has the potential to treat inflammation as well as bacterial and fungal infections. It exhibited selective antibacterial activity against Helicobacter pylori, without influencing the major normal gastrointestinal bacteria. Patchouli alcohol significantly accelerated the recovery of the UV-induced skin lesions, evidently through anti-oxidant and anti-inflammatory action, as well as down-regulation of the MMP-1 and MMP-3 expression. - Molecular Weight :222.36
- Purity :> 98%
Molecular Formula : C15H26O Canonical SMILES : CC1CCC2(C(C3CCC2(C1C3)C)(C)C)O InChI : InChI=1S/C15H26O/c1-10-5-8-15(16)13(2,3)11-6-7-14(15,4)12(10)9-11/h10-12,16H,5-9H2,1-4H3/t10-,11+,12-,14-,15+/m0/s1
InChIKey :
GGHMUJBZYLPWFD-CUZKYEQNSA-N
Appearance :
Powder
Application :
Antibacterial/anti-inflammatory
Synonyms :
1,6-Methanonaphthalen-1(2H)-ol, octahydro-4,8a,9,9-tetramethyl-, (1alpha,4beta,4aalpha,6beta,8aalpha)-; 1,6-Methanonaphthalen-1(2H)-ol, octahydro-4,8a,9,9-tetramethyl-, [1R-(1alpha,4beta,4aalpha,6beta,8aalpha)]-; Patchoulol; patchouli camphor; patchoulanol
More details are to be found here
BuGuCh & Partners
Germany
Description : Patchouli alcohol, coming from the herbs of Pogostemon cablin (Blanco) Benth, has the potential to treat inflammation as well as bacterial and fungal infections. It exhibited selective antibacterial activity against Helicobacter pylori, without influencing the major normal gastrointestinal bacteria. Patchouli alcohol significantly accelerated the recovery of the UV-induced skin lesions, evidently through anti-oxidant and anti-inflammatory action, as well as down-regulation of the MMP-1 and MMP-3 expression. - Molecular Weight :222.36
- Purity :> 98%
Molecular Formula : C15H26O Canonical SMILES : CC1CCC2(C(C3CCC2(C1C3)C)(C)C)O InChI : InChI=1S/C15H26O/c1-10-5-8-15(16)13(2,3)11-6-7-14(15,4)12(10)9-11/h10-12,16H,5-9H2,1-4H3/t10-,11+,12-,14-,15+/m0/s1
InChIKey :
GGHMUJBZYLPWFD-CUZKYEQNSA-N
Appearance :
Powder
Application :
Antibacterial/anti-inflammatory
Synonyms :
1,6-Methanonaphthalen-1(2H)-ol, octahydro-4,8a,9,9-tetramethyl-, (1alpha,4beta,4aalpha,6beta,8aalpha)-; 1,6-Methanonaphthalen-1(2H)-ol, octahydro-4,8a,9,9-tetramethyl-, [1R-(1alpha,4beta,4aalpha,6beta,8aalpha)]-; Patchoulol; patchouli camphor; patchoulanol
More details are to be found here
Santa Cruz Biotechnology, Inc.
USA
Description : Patchouli alcohol, coming from the herbs of Pogostemon cablin (Blanco) Benth, has the potential to treat inflammation as well as bacterial and fungal infections. It exhibited selective antibacterial activity against Helicobacter pylori, without influencing the major normal gastrointestinal bacteria. Patchouli alcohol significantly accelerated the recovery of the UV-induced skin lesions, evidently through anti-oxidant and anti-inflammatory action, as well as down-regulation of the MMP-1 and MMP-3 expression. - Molecular Weight :222.36
- Purity :> 98%
Molecular Formula : C15H26O Canonical SMILES : CC1CCC2(C(C3CCC2(C1C3)C)(C)C)O InChI : InChI=1S/C15H26O/c1-10-5-8-15(16)13(2,3)11-6-7-14(15,4)12(10)9-11/h10-12,16H,5-9H2,1-4H3/t10-,11+,12-,14-,15+/m0/s1
InChIKey :
GGHMUJBZYLPWFD-CUZKYEQNSA-N
Appearance :
Powder
Application :
Antibacterial/anti-inflammatory
Synonyms :
1,6-Methanonaphthalen-1(2H)-ol, octahydro-4,8a,9,9-tetramethyl-, (1alpha,4beta,4aalpha,6beta,8aalpha)-; 1,6-Methanonaphthalen-1(2H)-ol, octahydro-4,8a,9,9-tetramethyl-, [1R-(1alpha,4beta,4aalpha,6beta,8aalpha)]-; Patchoulol; patchouli camphor; patchoulanol
More details are to be found here
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