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Key Documents

D0138

Sigma-Aldrich

1,2-Dioleoyl-sn-glycerol

≥97%

Sinonimo/i:

(9Z)-9-Octadecenoic acid 1,1′-[(1S)-1-(hydroxymethyl)-1,2-ethanediyl] ester, (S)-1,2-Diolein, (S)-Glycerol 1,2-dioleate, 1,2-Di(cis-9-octadecenoyl)-sn-glycerol, DG(18:1(9Z)/18:1(9Z)/0:0), DG(18:1/18:1/0:0)

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About This Item

Formula empirica (notazione di Hill):
C39H72O5
Numero CAS:
Peso molecolare:
620.99
Beilstein:
1730457
Numero MDL:
Codice UNSPSC:
12352211
ID PubChem:
NACRES:
NA.25

Origine biologica

semisynthetic

Saggio

≥97%

Forma fisica

liquid

Impurezze

1,3-isomer, trace

Gruppo funzionale

ether

Tipo di lipide

neutral glycerides

Condizioni di spedizione

dry ice

Temperatura di conservazione

−20°C

Stringa SMILE

OC[C@H](OC(CCCCCCC/C=C\CCCCCCCC)=O)COC(CCCCCCC/C=C\CCCCCCCC)=O

InChI

1S/C39H72O5/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-38(41)43-36-37(35-40)44-39(42)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h17-20,37,40H,3-16,21-36H2,1-2H3/b19-17-,20-18-/t37-/m0/s1
AFSHUZFNMVJNKX-LLWMBOQKSA-N

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Applicazioni


  • Direct and simultaneous analysis of lipase-catalyzed hydrolysis of high-oleic oil model by chiral stationary phase HPLC-ELSD.: This study utilizes 1,2-dioleoyl-sn-glycerol to investigate lipase-catalyzed hydrolysis, providing insights into enzymatic processes and chiral analysis which are critical in food chemistry and biochemistry (Choi et al., 2022).

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


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Bio-protocol, 10(10), e3626-e3626 (2021-03-05)
It is important to experimentally determine how membrane proteins are integrated into biomembranes to unveil the roles of the integration factors, and to understand the functions and structures of membrane proteins. We have developed a reconstitution system for membrane protein
Keisuke Kobayashi et al.
Scientific reports, 8(1), 12099-12099 (2018-08-16)
Atropisomers with a biaryl dihydronaphthopyranone structure, dinapinones A1 (DPA1) (M position) and A2 (DPA2) (P position), were isolated from the fungus culture broth of Talaromyces pinophilus FKI-3864 as inhibitors of [14C]neutral lipid ([14C]triacylglycerol (TG) and [14C]cholesteryl ester (CE)) synthesis from
Ferdinand Ngale Njume et al.
PLoS neglected tropical diseases, 13(7), e0007591-e0007591 (2019-07-23)
Onchocerca volvulus is the nematode pathogen responsible for human onchocerciasis also known as "River blindness", a neglected tropical disease that affects up to 18 million people worldwide. Helminths Excretory Secretory Products (ESPs) constitute a rich repertoire of molecules that can
Peter Reinink et al.
European journal of immunology, 49(5), 737-746 (2019-03-12)
Lyme disease is a common multisystem disease caused by infection with a tick-transmitted spirochete, Borrelia burgdorferi and related Borrelia species. The monoglycosylated diacylglycerol known as B. burgdorferi glycolipid II (BbGL-II) is a major target of antibodies in sera from infected
Rachel N Cotton et al.
The Journal of clinical investigation, 131(1) (2021-01-05)
CD1a-autoreactive T cells contribute to skin disease, but the identity of immunodominant self-lipid antigens and their mode of recognition are not yet solved. In most models, MHC and CD1 proteins serve as display platforms for smaller antigens. Here, we showed

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