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109614

Sigma-Aldrich

Butyryl chloride

98%

Synonym(s):

Butanoic acid chloride, Butyric acid chloride, Butyric chloride, Butyroyl chloride, n-Butanoyl chloride, n-Butyroyl chloride, n-Butyryl chloride

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About This Item

Linear Formula:
CH3CH2CH2COCl
CAS Number:
141-75-3
Molecular Weight:
106.55
Beilstein/REAXYS Number:
605395
EC Number:
205-498-5
MDL number:
MFCD00000752
UNSPSC Code:
12352100
PubChem Substance ID:
24846927
NACRES:
NA.22

vapor density

3.7 (vs air)

Quality Level

200

assay

98%

refractive index

n20/D 1.412 (lit.)

bp

102 °C (lit.)

mp

−89 °C (lit.)

density

1.026 g/mL at 25 °C (lit.)

SMILES string

CCCC(Cl)=O

InChI

1S/C4H7ClO/c1-2-3-4(5)6/h2-3H2,1H3

InChI key

DVECBJCOGJRVPX-UHFFFAOYSA-N

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Related Categories

Application

Butyryl chloride has been used to esterify wood meal dissolved in the ionic liquid, 1-butyl-3-methylimidazolium chloride.

signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B

wgk_germany

WGK 1

flash_point_f

64.4 °F

flash_point_c

18 °C

ppe

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Tongqi Yuan et al.
Bioresource technology, 102(6), 4590-4593 (2011-01-25)
Wood meal was dissolved under identical conditions in the ionic liquid 1-butyl-3-methylimidazolium chloride ([C(4)mim]Cl) and homogeneously esterified with butyryl chloride and lauroyl chloride in the presence of triethylamine as a neutralizer. The effect of the molar ratio of reagent to
Paulina Majewska
Bioorganic chemistry, 61, 28-35 (2015-06-13)
2-Hydroxy-2-(ethoxyphenylphosphinyl)acetic acid, a new type of organophosphorus compound possessing two stereogenic centers, was investigated. Racemic 2-butyryloxy-2-(ethoxyphenylphosphinyl)acetic acid was synthesized and hydrolyzed using four bacterial species as biocatalysts. In all cases the reaction was more or less stereoselective and isomers bearing
Janclei P Coutinho et al.
Talanta, 134, 256-263 (2015-01-27)
In this work a multivariate statistical tool (Derringer and Suich optimization) was proposed for the separation of seventeen capsinoids (natural and synthetic) using the UHPLC-DAD chromatography. Capsinoids were analyzed at 280 nm. The variables optimized were the mobile phase (water

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