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157422

Isovaleryl chloride

Name: Isovaleryl chloride
Brand: ALDRICH

98%

Synonym(s):

3-Methylbutyryl chloride

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About This Item

Linear Formula:

(CH₃)₂CHCH₂COCl

CAS Number:

108-12-3

Molecular Weight:

120.58

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24849677

EC Number:

203-552-2

Beilstein/REAXYS Number:

741910

MDL number:

MFCD00000738

Assay:

98%

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Properties

Quality Level

200

assay

98%

refractive index

n20/D 1.416 (lit.)

bp

115-117 °C (lit.)

density

0.989 g/mL at 25 °C (lit.)

functional group

acyl chloride

SMILES string

CC(C)CC(Cl)=O

InChI

1S/C5H9ClO/c1-4(2)3-5(6)7/h4H,3H2,1-2H3

InChI key

ISULZYQDGYXDFW-UHFFFAOYSA-N

Description

Application

Isovaleryl chloride was used in the synthesis of:

furanodictines A and B
tetrapeptide amide, S-benzyl-L-cysteinyl-L-prolyl-L-leucylglycinamide
(+)-blastmycinone
(R)- and (S)-2-methyl-4-octanol, aggregation pheromone of some sugarcane weevils

signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Flam. Liq. 3 - Skin Corr. 1B

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

87.8 °F - closed cup

flash_point_c

31 °C - closed cup

ppe

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

Regulatory Information

危险化学品

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Enantioselective synthesis of (R)-and (S)-2-methyl-4-octanol, the male-produced aggregation pheromone of Curculionidae species.

Baraldi PT, et al.

Tetrahedron Asymmetry, 13(6), 621-624 (2002)

The Synthesis of the Tetrapeptide Amide S-Benzyl-L-cysteinyl-L-prolyl-L-leucylglycinamide

Ressler Cand Vincent du Vigneaud.

Journal of the American Chemical Society, 76(12), 3107-3109 (1954)

Novel and facile synthesis of furanodictines A and B based on transformation of 2-acetamido-2-deoxy-D-glucose into 3,6-anhydro hexofuranoses.

Makoto Ogata et al.

Carbohydrate research, 345(2), 230-234 (2009-12-08)

A novel synthesis of furanodictines A [2-acetamido-3,6-anhydro-2-deoxy-5-O-isovaleryl-D-glucofuranose (1)] and B [2-acetamido-3,6-anhydro-2-deoxy-5-O-isovaleryl-D-mannofuranose (2)] is described starting from 2-acetamido-2-deoxy-D-glucose (GlcNAc). The synthetic protocol is based on deriving the epimeric bicyclic 3,6-anhydro sugars [2-acetamido-3,6-anhydro-2-deoxy-D-glucofuranose (4) and 2-acetamido-3,6-anhydro-2-deoxy-D-mannofuranose (5)] from GlcNAc. Reaction with borate

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Global Trade Item Number

SKU	GTIN
157422-100G	04061838743329
157422-25G	04061838743336
157422-500G	04061838743343