13002-10-3

• 

• Basic information

  1. Product Name: 1,1-Dibutoxypropane
  2. Synonyms: 1,1-Dibutoxypropane
  3. CAS NO:13002-10-3
  4. Molecular Formula: C₁₁H₂₄O₂
  5. Molecular Weight: 188.31
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 13002-10-3.mol
  9. Article Data: 4

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 205.1°C at 760 mmHg
  3. Flash Point: 49.3°C
  4. Appearance: /
  5. Density: 0.843g/cm³
  6. Vapor Pressure: 0.364mmHg at 25°C
  7. Refractive Index: 1.419
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 1,1-Dibutoxypropane(CAS DataBase Reference)
  11. NIST Chemistry Reference: 1,1-Dibutoxypropane(13002-10-3)
  12. EPA Substance Registry System: 1,1-Dibutoxypropane(13002-10-3)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 13002-10-3(Hazardous Substances Data)

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• Usage
• SDS
• Upstream product
• Downstream Products
• Article

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• 1,1-DIBUTOXYPROPANECAS

  Cas No: 13002-10-3

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• Hangzhou Fandachem Co.,Ltd
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• 1,1-Dibutoxypropane

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13002-10-3 Usage

Physical state

Colorless, slightly viscous liquid

Industrial applications

a. Solvent in the production of paints, coatings, and adhesives
b. Coupling agent
c. Component in some cleaning products

Potential uses

Agricultural chemical (due to pesticidal properties)

Safety precautions

a. Irritant to eyes
b. Irritant to skin
c. Irritant to respiratory system
d. Proper safety measures should be followed when handling

Check Digit Verification of cas no

The CAS Registry Mumber 13002-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,0 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13002-10:
(7*1)+(6*3)+(5*0)+(4*0)+(3*2)+(2*1)+(1*0)=33
33 % 10 = 3
So 13002-10-3 is a valid CAS Registry Number.

InChI:InChI=1/C11H24O2/c1-4-7-9-12-11(6-3)13-10-8-5-2/h11H,4-10H2,1-3H3

13002-10-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name	1-(1-butoxypropoxy)butane

1.2 Other means of identification

Product number	-
Other names	Propionaldehyd-dibutylacetal

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13002-10-3 SDS

13002-10-3Upstream product

• 3739-64-8 allyl n-butyl ether 
• 6032-29-7 (+/-)-2-pentanol 
• 108-95-2 phenol 
• 71-36-3 butan-1-ol 
• 100-51-6 benzyl alcohol 
• 588-43-2 Tributyl orthoformate 
• 97-93-8 triethylaluminum 
• 123-38-6 propionaldehyde 
• 45094-50-6 1,1-dibutoxy-prop-2-en 

13002-10-3Downstream Products

• 123-38-6 propionaldehyde 

13002-10-3Relevant articles and documents

A selective and convenient ruthenium mediated method for the synthesis of mixed acetals and orthoesters

Krompiec, Stanis?aw,Penczek, Robert,Ku?nik, Nikodem,Ma?ecki, Jan Grzegorz,Matlengiewicz, Marek

, p. 137 - 140 (2007)

Addition of alcohols and phenols to O-allyl compounds (allyl ethers and acrolein acetals), catalyzed by [RuCl2(PPh3)3], was examined. Intramolecular addition of an OH group, leading to the formation of cyclic acetals and o

Reactions of trialkylalanes with cyclic acetals and orthoformates in CH2Cl2 and ClCH2CH2Cl as solvents

Gafarova,Dekhtyar',Dekhtyar',Fatykhov,Spirikhin,Vostrikova,Zlotskii,Dokichev

, p. 1003 - 1008 (2007/10/03)

Under mild conditions, trialkylalanes (Et3Al and Bu i3Al) in chlorine-containing solvents (CH 2Cl2 or ClCH2CH2Cl) react with cyclic acetals and orthoformates to form glycol monoethers and dialkylacetals, respectively, in high yields. The 1H NMR spectroscopic data demonstrate that CH2Cl2 or ClCH2CH 2Cl interacts with Bui3Al.

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