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Merck
CN

W291501

聚山梨酯20

别名:

Cremophor PS 20, Monebatt - 20

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关于此项目

化学文摘社编号:
FEMA Number:
2915
UNSPSC Code:
12164502
NACRES:
NA.21
MDL number:
Organoleptic:
alcohol
Food allergen:
no known allergens
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SMILES string

O1C(C(C(C1)OCCO)OCCO)C(OCCO)COCCOC(=O)CCCCCCCCCCC

InChI

1S/C26H50O10/c1-2-3-4-5-6-7-8-9-10-11-24(30)34-19-18-31-20-22(32-15-12-27)26-25(35-17-14-29)23(21-36-26)33-16-13-28/h22-23,25-29H,2-21H2,1H3

InChI key

HMFKFHLTUCJZJO-UHFFFAOYSA-N

reg. compliance

FDA 21 CFR 172.515, FDA 21 CFR 173.310, FDA 21 CFR 175.105, FDA 21 CFR 178.3400

description

Biological source: corn or palm

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

no known allergens

organoleptic

alcohol

Quality Level

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General description

聚山梨酯 20 是一种亲水性非离子表面活性剂,常用作乳化剂、分散剂和增溶剂。

Application

聚山梨醇酯 20 已被用于一项研究,以评估其作为公认的安全 (GRAS) 增塑剂在赋予巴西棕榈蜡可塑性方面的潜力。

Disclaimer

仅供R&D或非EU食品使用不用于零售。

存储类别

10 - Combustible liquids

flash_point_f

527.0 °F - Pensky-Martens closed cup

flash_point_c

275 °C - Pensky-Martens closed cup

ppe

Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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CRC Handbook of Food, Drug, and Cosmetic Excipients, 295-296 (1992)
Plasticisation of carnauba wax with generally recognised as safe (GRAS) additives.
Zhang Y, et al.
Polymer, 86, 208-219 (2016)
Julie Beegle et al.
Stem cells (Dayton, Ohio), 33(6), 1818-1828 (2015-02-24)
Mesenchymal stem cells/multipotent stromal cells (MSCs) are promising therapeutics for a variety of conditions. However, after transplantation, cell retention remains extremely challenging. Given that many hypoxic signals are transitory and that the therapeutic administration of MSCs is typically into tissues
Daniel C Zielinski et al.
Nature communications, 6, 7101-7101 (2015-06-10)
Drug side effects cause a significant clinical and economic burden. However, mechanisms of drug action underlying side effect pathogenesis remain largely unknown. Here, we integrate pharmacogenomic and clinical data with a human metabolic network and find that non-pharmacokinetic metabolic pathways

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