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Butylate

Basic information Safety Supplier Related

Butylate Basic information

Product Name:
Butylate
Synonyms:
  • Butylate Standard
  • anelda
  • aneldazine
  • bis(2-methylpropyl)-carbamothioicacis-ethylester
  • butilate
  • Carbamic acid, diisobutylthio-, S-ethyl ester
  • Carbamothioic acid, bis(2-methylpropyl)-, S-ethyl ester
  • Diisobutylthiocarbamic acid S-ethyl ester
CAS:
2008-41-5
MF:
C11H23NOS
MW:
217.37
EINECS:
217-916-3
Product Categories:
  • Alphabetic
  • B
  • BI - BZPesticides&Metabolites
  • Herbicides
  • Thiocarbamates
Mol File:
2008-41-5.mol
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Butylate Chemical Properties

Melting point:
<25 °C
Boiling point:
130°C (10 mmHg)
Density 
0.9402
refractive index 
nD30 1.4701
storage temp. 
0-6°C
pka
-1.22±0.70(Predicted)
form 
Liquid
color 
Amber
Water Solubility 
45mg/L(room temperature)
Merck 
13,1545
BRN 
1770420
CAS DataBase Reference
2008-41-5(CAS DataBase Reference)
NIST Chemistry Reference
Carbamothioic acid, bis(2-methylpropyl)-, s-ethyl ester(2008-41-5)
EPA Substance Registry System
Butylate (2008-41-5)
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Safety Information

Hazard Codes 
Xn;N,N,Xn
Risk Statements 
20-51/53
Safety Statements 
60
RIDADR 
UN 3082
WGK Germany 
2
RTECS 
EZ7525000
HS Code 
29033080
Hazardous Substances Data
2008-41-5(Hazardous Substances Data)
Toxicity
LD50 oral in rat: 4gm/kg

MSDS

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Butylate Usage And Synthesis

Description

Butylate is a clear liquid with an aromaticodor. Molecular weight = 217.4; Specific gravity 5 0.94;Boiling point = 130C at 10 mmHg at 20C; Vaporpressure 5 1 3 10 2 3 mmHg. Low solubility in water; solubility5 44 mg/L

Chemical Properties

Butylate is a clear liquid with an aromatic odor.

Uses

Herbicide.

Definition

ChEBI: Butylate is a tertiary amine.

Agricultural Uses

Herbicide: Classified as a General Use Pesticide (GUP) with applications limited to corn fields. Not approved for use in EU countries. A selective herbicide for use on field corn, sweet corn, and popcorn to control grassy and broadleaf weeds and seeds in the soil prior to sowing a crop. Often applied in combination with atrazine and/or cyanazine.

Trade name

ANELDA PLUS®; ANELDAZIN®; ANELIROX®; ATRA-BUTE®[C] Nov.1992; BUTILATE®; GENATE®[C] August 1994; R-1910®[C] Dec.1987; STAUFFER R-1910®[C] Dec.1987; SUTAN®[C] Sept.1994; SUTAZINE®[C] Dec.1987; TOMAHAWK®

Potential Exposure

A thiocarbamate herbicide. A potential danger to those involved in the manufacture, formulation or application of this carbamate herbicide which is used to control weed seeds in the soil prior to sowing crops

First aid

If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seekmedical attention immediately. If this chemical contactsthe skin, remove contaminated clothing and wash immediately with soap and water. Seek medical attention immediately. If this chemical has been inhaled, remove fromexposure, begin rescue breathing (using universal precautions, including resuscitation mask) if breathing hasstopped and CPR if heart action has stopped. Transferpromptly to a medical facility. When this chemical hasbeen swallowed, get medical attention. Give large quantities of water and induce vomiting. Do not make an unconscious person vomit.

storage

Color Code—Green: General storage may be used.Prior to working with this chemical you should be trainedon its proper handling and storage. Store in tightly closedcontainers in a cool, dry place.

Shipping

UN3082 Environmentally hazardous substances, liquid, n.o.s., Hazard class: 9; Labels: 9—Miscellaneous hazardous material, Technical Name Required

Incompatibilities

Thiocarbamate esters are combustible. They react violently with powerful oxidizers such as calcium hypochlorite. Poisonous gases are generated by the thermal decomposition of thiocarbamate compounds, including carbon disulfide, oxides of sulfur, oxides of nitrogen, hydrogen sulfide, ammonia, and methylamine. Many materials in this group slowly decompose in aqueous solution to form carbon disulfide and methylamine or other amines. Such decompositions are accelerated by acids. Flammable gases are generated by the combination of thiocarbamates with aldehydes, nitrides, and hydrides. Thiocarbamates are incompatible with acids, peroxides, and acid halides

ButylateSupplier

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