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Merck
CN

19270

丁酸酐

purum, ≥97.0% (NT)

别名:

丁酐

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关于此项目

线性分子式:
(CH3CH2CH2CO)2O
化学文摘社编号:
分子量:
158.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-383-4
Beilstein/REAXYS Number:
1099474
MDL number:
Assay:
≥97.0% (NT)
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产品名称

丁酸酐, purum, ≥97.0% (NT)

InChI key

YHASWHZGWUONAO-UHFFFAOYSA-N

InChI

1S/C8H14O3/c1-3-5-7(9)11-8(10)6-4-2/h3-6H2,1-2H3

SMILES string

CCCC(=O)OC(=O)CCC

vapor density

5.45 (vs air)

vapor pressure

10 mmHg ( 79.5 °C)

grade

purum

assay

≥97.0% (NT)

autoignition temp.

535 °F

expl. lim.

1.1 %, 104 °F
7.6 %, 144 °F

refractive index

n20/D 1.413 (lit.)
n20/D 1.413

bp

198-199 °C (lit.)

mp

−75-−66 °C (lit.)

solubility

alcohol: soluble (with decomposition)(lit.)
diethyl ether: soluble(lit.)
water: soluble (with decomposition)(lit.)

density

0.967 g/mL at 25 °C (lit.)

functional group

anhydride
ester

Quality Level

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Application

Butyric anhydride was used in the synthesis of:
  • dibutyrylchitin, a lipophilic chitin diester
  • N-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-n-butyramide
  • butyric-ester derivatives of hyaluronic acid

pictograms

CorrosionExclamation mark

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

supp_hazards

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 1

flash_point_f

188.6 °F - closed cup

flash_point_c

87 °C - closed cup

ppe

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

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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D Coradini et al.
International journal of cancer, 81(3), 411-416 (1999-04-21)
The potential clinical utility of sodium butyrate, a natural compound known to inhibit tumor-cell growth, is hampered by the difficulty of achieving effective in-vivo concentrations. The short half-life (about 5 minutes) of sodium butyrate results in rapid metabolism and excretion.
Nabilah Abdul Hadi et al.
Foods (Basel, Switzerland), 9(1) (2020-01-17)
Rice and quinoa starch esters were prepared by acylation using short-chain fatty acid anhydrides with different chain lengths (acetic, propionic, and butyric anhydride). A direct stoichiometric method based on the acylation reaction was used to determine the degree of substitution
J J Kaylor et al.
Carbohydrate research, 331(4), 439-444 (2001-06-12)
The syntheses of four analogues of N4-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-L-asparagine are described. Activated carboxylic acids were reacted with 2-acetamido-2-deoxy-beta-D-glucopyranosylamine. n-Butyric anhydride gave N-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-n-butyramide. 3-Chloropropionic anhydride was synthesized from 3-chloropropionic acid and gave N-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-3-chloropropionamide. Equilibration of the latter with ammonium bicarbonate gave N1-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-3-aminopropionamide. Succinimidyl
Xiaoning Shan et al.
International journal of pharmaceutics, 590, 119884-119884 (2020-09-21)
Poly(2-methyl-2-oxazoline) (PMOZ), poly(2-propyl-2-oxazoline) (PnPOZ) and poly(2-isopropyl-2-oxazoline) (PiPOZ) were synthesized by hydrolysis of 50 kDa poly(2-ethyl-2-oxazoline) (PEOZ) and subsequent reaction of the resulting poly(ethylene imine) with acetic, butyric and isobutyric anhydrides, respectively. These polymers were characterized by proton nuclear magnetic resonance, FTIR
Luca Casettari et al.
Drug development and industrial pharmacy, 38(8), 979-984 (2011-11-30)
Dibutyrylchitin (DBC), a lipophilic chitin diester, has been synthesized from chitin and butyric anhydride with methanesulfonic acid as catalyst. Exhaustive esterification of free alcoholic groups of chitin was assessed by FT-IR and (1)H-NMR spectroscopy. High degree of alkyl substitution allowed

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