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Merck

213705

Sigma-Aldrich

1,2-辛二醇

98%

别名:

(±)-辛烷-1,2-二醇, 1,2-八亚甲基二醇, 1,2-辛二醇, 7,8-八亚甲基二醇, 正辛烷-1,2-二醇, 辛甘醇

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About This Item

线性分子式:
CH3(CH2)5CH(OH)CH2OH
CAS号:
分子量:
146.23
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

蒸汽密度

>1 (vs air)

品質等級

化驗

98%

形狀

solid

bp

131-132 °C/10 mmHg (lit.)

mp

36-38 °C (lit.)

官能基

hydroxyl

SMILES 字串

CCCCCCC(O)CO

InChI

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

InChI 密鑰

AEIJTFQOBWATKX-UHFFFAOYSA-N

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一般說明

1,2-辛二醇是一种潜在的杀虫剂,临床上可用于治疗头虱侵扰

應用

1,2-辛二醇用作有机改性剂,以改善有机酸和碱的HPLC分离。它也用于制备卤代醇棕榈酸酯

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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分析证书(COA)

Lot/Batch Number

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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
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
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
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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