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Merck
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文件

16511

Sigma-Aldrich

3-溴丁酸

≥95.0% (GC)

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About This Item

线性分子式:
CH3CHBrCH2COOH
CAS号:
2623-86-1
分子量:
167.00
Beilstein:
1720574
EC號碼:
220-082-3
MDL號碼:
MFCD00053318
分類程式碼代碼:
12352100
PubChem物質ID:
57647573
NACRES:
NA.22

化驗

≥95.0% (GC)

折射率

n20/D 1.476

密度

1.57 g/mL at 20 °C (lit.)

SMILES 字串

CC(Br)CC(O)=O

InChI

1S/C4H7BrO2/c1-3(5)2-4(6)7/h3H,2H2,1H3,(H,6,7)

InChI 密鑰

HAIUIAZIUDPZIE-UHFFFAOYSA-N

應用

3-Bromobutyric acid was used in the synthesis of β-butyrolactone, monomer for a naturally occurring polyester, D-poly-β-hydroxybutyrate. It was used to investigate the effect of halo acids on the activity of aspartate aminotransferase isoenzymes in their pyridoxamine form. It was also used in the synthesis of optically active β-lactones.

象形圖

Corrosion
GHS05

訊號詞

Danger

危險聲明

H314

危險分類

Eye Dam. 1 - Skin Corr. 1B

儲存類別代碼

8A - Combustible corrosive hazardous materials

水污染物質分類（WGK）

WGK 3

閃點（°F）

237.2 °F - closed cup

閃點（°C）

114 °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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Synthesis and characterization of poly-?-hydroxybutyrate. I. Synthesis of crystalline DL-poly-?-hydroxybutyrate from DL-?-butyrolactone.
Agostini DE, et al.
Journal of Polymer Science: Part A, General Papers, 9(10), 2775-2787 (1971)
Methods for the synthesis of optically active β-lactones (2-oxetanones).
Yang YW and Romo D.
Tetrahedron, 55(21), 6403-6434 (1999)
Selective inactivation of pyridoxamine form of aspartate aminotransferase by iodoacetate. Carboxymethylation of 4'-amino group of bound pyridoxamine 5'-phosphate.
Y Morino et al.
The Journal of biological chemistry, 253(17), 6026-6030 (1978-09-10)

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