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Merck

W292419

Sigma-Aldrich

丙酸

greener alternative

natural, 99%, FG

别名:

Propanoic acid, Propanyl acid, 初油酸

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About This Item

线性分子式:
CH3CH2COOH
CAS号:
分子量:
74.08
FEMA號碼:
2924
Beilstein:
506071
EC號碼:
歐洲委員會號碼:
3c
MDL號碼:
分類程式碼代碼:
12164502
PubChem物質ID:
Flavis號碼:
8.003
NACRES:
NA.21

等級

FG
Fragrance grade
Halal
Kosher
natural

品質等級

agency

follows IFRA guidelines

法律遵循

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 178.1010

蒸汽密度

2.55 (vs air)

蒸汽壓力

2.4 mmHg ( 20 °C)

化驗

99%

自燃溫度

955 °F

expl. lim.

12.1 %

環保替代產品特色

Less Hazardous Chemical Syntheses
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

折射率

n20/D 1.386 (lit.)

bp

141 °C (lit.)

mp

−24-−23 °C (lit.)

溶解度

H2O: soluble
soluble

密度

0.993 g/mL at 25 °C (lit.)

應用

flavors and fragrances

文件

see Safety & Documentation for available documents

食物過敏原

no known allergens

香料過敏原

no known allergens

環保替代類別

感官的

dairy; acidic; pungent

SMILES 字串

CCC(O)=O

InChI

1S/C3H6O2/c1-2-3(4)5/h2H2,1H3,(H,4,5)

InChI 密鑰

XBDQKXXYIPTUBI-UHFFFAOYSA-N

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一般說明

Propionic acid (PA) is a naturally occurring carboxylic acid, which is an excellent raw material as it is stable, cheap, and safe and can even be used as a food additive.
Propionic acid is a volatile fatty acid (VFA) formed in the rumen of ruminants by bacterial fermentations.
We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives . This product is a Biobased products, showing key improvements in Green Chemistry Principles “Less Hazardous Chemical Syntheses” and “Use of Renewable Feedstock”.

訊號詞

Danger

危險聲明

危險分類

Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

129.2 °F - closed cup

閃點(°C)

54 °C - closed cup

個人防護裝備

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


分析证书(COA)

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Interconversions and production of volatile fatty acids in the sheep rumen.
Bergman EN, et al.
The Biochemical Journal, 97(1), 53-58 (1965)
Metabolism of propionic acid in animal tissues I. Enzymatic conversion of propionate to succinate.
Flavin M & Ochoa S.
The Journal of Biological Chemistry, 229(2), 965-979 (1957)
Nucleophilic ?-Carbon Activation of Propionic Acid as a 3-Carbon Synthon by Carbene Organocatalysis
Jin, Zhichao, et al.
Chemistry?A European Journal, 21 (26), 9360-9363 (2015)
Flour and Breads and their Fortification in Health and Disease Prevention.
Victor R. Preedy, Ronald Ross Watson, Vinood B
Technology & Engineering, 476-476 (2011)
Biological effects of propionic acid in humans; metabolism, potential applications and underlying mechanisms
Sa'ad, H., et al.
Molecular and Cellular Biology, 1801 (11), 1175-1183 (2010)

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