14462

(−)-α-Bisabolol

≥93% (GC)

Manufacturer: Sigma Aldrich

CAS Number: 23089-26-1

Synonym(S): (-)-alpha-Bisabolol, (−)-6-Methyl-2-(4-methyl-3-cyclohexen-1-yl)-5-hepten-2-ol, Levomenol

Select a Size

Pack Size SKU Availability Price
5 ML 14462-5-ML In Stock ₹ 4,860.43
25 ML 14462-25-ML In Stock ₹ 13,693.63

14462 - 5 ML

₹ 4,860.43

In Stock

Quantity

1

Base Price: ₹ 4,860.43

GST (18%): ₹ 874.877

Total Price: ₹ 5,735.307

Quality Level

100

Assay

≥93% (GC)

optical activity

[α]/D -58±5°, neat

refractive index

n20/D 1.496

SMILES string

C\C(C)=C\CC[C@](C)(O)[C@H]1CCC(C)=CC1

InChI

1S/C15H26O/c1-12(2)6-5-11-15(4,16)14-9-7-13(3)8-10-14/h6-7,14,16H,5,8-11H2,1-4H3/t14-,15+/m1/s1

InChI key

RGZSQWQPBWRIAQ-CABCVRRESA-N

Other Options

Image Product Name Manufacturer Price Range
11-101-9010
(-)-Bisabolol, ≥93% (GC), MilliporeSigma™ Supelco™
MilliporeSigma Supelco ₹ 13,946.28
11-101-7828
TraceCERT™ (-)-α-Bisabolol, 2,000 μg/mL in Methanol, MilliporeSigma™ Supelco™
MilliporeSigma Supelco ₹ 10,951.68
50-175-1793
Sigma Aldrich Fine Chemicals Biosciences (-)-alpha-Bisabolol primary reference standard | 23089-26-1 | MFCD03412455 | 100MG
Sigma Aldrich Fine Chemicals Biosciences ₹ 28,298.97
95426
(−)-α-Bisabolol
Supelco ₹ 11,885.85
PHR3196
Levomenol
Supelco ₹ 19,084.48
1362307
Levomenol
Sigma Aldrich ₹ 40,550.45
PHL80005
(−)-α-Bisabolol
Sigma Aldrich ₹ 28,047.58
AI45466
23089-26-1 | 3-Cyclohexene-1-methanol, a,4-dimethyl-a-(4-methyl-3-pentenyl)-,(aS,1S)-
A2B Chem ₹ 3,080.16 - ₹ 19,593.24

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Description

  • General description: (-)-α-Bisabolol is the major constituent of essential oil from leaves of Hymenocrater yazdianus[1].
  • Application: (-)-α-Bisabolol was used to investigate the leishmanicidal and cytotoxic activity of essential oil of Vanillosmopsis arborea[2].
  • Biochem/physiol Actions: α-Bisabolol is active against primary acute leukemia cells, including BCR-ABL(+) acute lymphoblastic leukemias[3]. It is the inhibitor of voltage-dependent Ca(2+) channels in tracheal smooth muscle preparations of rat[4]. It also inhibits human and rat glioma cell growth and survival[1]. It is a potential new therapeutic agent against leishmaniasis[2].

SAFETY INFORMATION

Hazard Statements

H412

Precautionary Statements

P273 - P501

Hazard Classifications

Aquatic Chronic 3

WGK

WGK 1

Flash Point(F)

289.4 °F

Flash Point(C)

143 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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100

Assay:
≥93% (GC)

optical activity:
[α]/D -58±5°, neat

refractive index:
n20/D 1.496

SMILES string:
C\C(C)=C\CC[C@](C)(O)[C@H]1CCC(C)=CC1

InChI:
1S/C15H26O/c1-12(2)6-5-11-15(4,16)14-9-7-13(3)8-10-14/h6-7,14,16H,5,8-11H2,1-4H3/t14-,15+/m1/s1

InChI key:
RGZSQWQPBWRIAQ-CABCVRRESA-N

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NC(=O)C(F)(F)F

InChI:
1S/C2H2F3NO/c3-2(4,5)1(6)7/h(H2,6,7)

InChI key:
NRKYWOKHZRQRJR-UHFFFAOYSA-N

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O.[Na+].N[C@@H](CCC([O-])=O)C(O)=O

InChI:
1S/C5H9NO4.Na.H2O/c6-3(5(9)10)1-2-4(7)8;;/h3H,1-2,6H2,(H,7,8)(H,9,10);;1H2/q;+1;/p-1/t3-;;/m0../s1

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GJBHGUUFMNITCI-QTNFYWBSSA-M

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