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Merck
모든 사진(3)

주요 문서

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213705

Sigma-Aldrich

1,2-Octanediol

98%

동의어(들):

(±)-Octane-1,2-diol, 1,2-Dihydroxyoctane, 1,2-Octylene glycol, 7,8-Dihydroxyoctane, Caprylyl glycol, n-Octane-1,2-diol

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모든 사진(3)

About This Item

Linear Formula:
CH3(CH2)5CH(OH)CH2OH
CAS Number:
1117-86-8
Molecular Weight:
146.23
EC Number:
214-254-7
MDL number:
MFCD00010738
UNSPSC 코드:
12352100
PubChem Substance ID:
24852793
NACRES:
NA.22

vapor density

>1 (vs air)

Quality Level

200

분석

98%

형태

solid

bp

131-132 °C/10 mmHg (lit.)

mp

36-38 °C (lit.)

작용기

hydroxyl

SMILES string

CCCCCCC(O)CO

InChI

1S/C8H18O2/c1-2-3-4-5-6-8(10)7-9/h8-10H,2-7H2,1H3

InChI key

AEIJTFQOBWATKX-UHFFFAOYSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

일반 설명

1,2-Octanediol is a potential pediculicide and is useful for treating head louse infestation clinically.

애플리케이션

1,2-Octanediol was used as organic modifier to improve the HPLC separation of organic acids and bases. It was also used in preparation of halohydrin palmitates.

픽토그램

Exclamation mark
GHS07

신호어

Warning

유해 및 위험 성명서

H319

Hazard Classifications

Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)

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시험 성적서(COA)

Lot/Batch Number
STBH3026
STBH6967
STBH4770
STBH1186
STBG6060V

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특정 버전이 필요한 경우 로트 번호나 배치 번호로 특정 인증서를 찾을 수 있습니다.

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문서 라이브러리 방문

Ian F Burgess et al.
PloS one, 7(4), e35419-e35419 (2012-04-24)
Interest in developing physically active pediculicides has identified new active substances. The objective was to evaluate a new treatment for clinical efficacy. We describe the selection of 1,2-octanediol as a potential pediculicide. Clinical studies were community based. The main outcome
Mireia Oromí-Farrús et al.
Molecules (Basel, Switzerland), 14(10), 4275-4283 (2009-11-20)
Preparation of (S)-1-chloro-2-octanol and (S)-1-bromo-2-octanol was carried out by the enzymatic hydrolysis of halohydrin palmitates using biocatalysts. Halohydrin palmitates were prepared by various methods from palmitic acid and 1,2-octanediol. A tandem hydrolysis was carried out using lipases from Candida antarctica
Shelly Li et al.
Journal of chromatography. A, 964(1-2), 91-98 (2002-08-30)
A straight-chain alcohol or diol additive in the mobile phase was used to modify and improve the HPLC separation of organic acids and bases. Incorporation of 2% 1-butanol, 1% 1,2-hexanediol, or 0.25% 1,2-octanediol into an aqueous mobile phase greatly improved
Kelli L Hvorecny et al.
Structure (London, England : 1993), 25(5), 697-707 (2017-04-11)
Pseudomonas aeruginosa secretes an epoxide hydrolase with catalytic activity that triggers degradation of the cystic fibrosis transmembrane conductance regulator (CFTR) and perturbs other host defense networks. Targets of this CFTR inhibitory factor (Cif) are largely unknown, but include an epoxy-fatty

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