218367
(S)-(−)-Limonene
96%
동의어(들):
(−)-p-Mentha-1,8-diene, (−)-Carvene, (S)-4-Isopropenyl-1-methyl cyclohexene
로그인조직 및 계약 가격 보기
크기 선택
제품정보 (DICE 배송 시 비용 별도)
실험식(Hill 표기법):
C10H16
CAS 번호:
Molecular Weight:
136.23
Beilstein:
2323991
EC Number:
MDL number:
UNSPSC 코드:
12352002
PubChem Substance ID:
NACRES:
NA.22
vapor density
4.7 (vs air)
Quality Level
vapor pressure
<3 mmHg ( 14.4 °C)
1 mmHg ( 20 °C)
분석
96%
양식
liquid
광학 활성
[α]19/D −94°, c = 10 in ethanol
expl. lim.
6.1 %
refractive index
n20/D 1.471 (lit.)
bp
175-177 °C (lit.)
density
0.844 g/mL at 25 °C (lit.)
SMILES string
CC(=C)[C@H]1CCC(C)=CC1
InChI
1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,10H,1,5-7H2,2-3H3/t10-/m1/s1
InChI key
XMGQYMWWDOXHJM-SNVBAGLBSA-N
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일반 설명
(S)-(-)-Limonene, a monoterpenoid compound, is mostly used in perfumery and in flavoring. On irradiation, it undergoes radiolysis, which leads to a reduction in the optical purity. (S)-(-)-Limonene also shows potent antimicrobial activity.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 3 - Skin Irrit. 2 - Skin Sens. 1B
Storage Class Code
3 - Flammable liquids
WGK
WGK 2
Flash Point (°F)
123.8 °F - closed cup
Flash Point (°C)
51 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Antimicrobial activity of limonene enantiomers and 1, 8-cineole alone and in combination.
Van Vuuren SF and Viljoen AM.
Flavour and Fragrance Journal, 22(6), 540-544 (2007)
Malaria parasites produce volatile mosquito attractants.
Kelly M, et al.
mBio, 6(2), e00235-e00215 (2015)
Gamma-radiolysis of chiral molecules: R (+)-limonene, S (-)-limonene and R (-)-a-phellandrene.
Cataldo F, et al.
J. Radioanal. Nucl. Chem., 262(2), 423-428 (2004)
P L Crowell et al.
Critical reviews in oncogenesis, 5(1), 1-22 (1994-01-01)
The naturally occurring monoterpene d-limonene has chemopreventive and chemotherapeutic activity against many rodent solid tumor types. The chemopreventive activity of limonene during initiation can be attributed to the induction of phase I and phase II enzymes, with resulting carcinogen detoxification.
P A Cornwell et al.
The Journal of pharmacy and pharmacology, 46(12), 938-950 (1994-12-01)
Wide-angle X-ray-diffraction experiments were used to investigate the molecular organization of barrier components of human stratum corneum. Diffraction lines related to the side-by-side lipid packing arrangements in the intercellular bilayers were identified as were patterns arising from secondary protein structures
Chromatograms
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